Abstract
Anna Leonov1, Anthony Arlia-Ciommo1, Simon D. Bourque1, Olivia Koupaki1, Pavlo Kyryakov1, Paméla Dakik1, Mélissa McAuley1, Younes Medkour1, Karamat Mohammad1, Tamara Di Maulo1 and Vladimir I. Titorenko1
1 Department of Biology, Concordia University, Montreal, Quebec, Canada
Correspondence to:
Vladimir I. Titorenko, email:
Keywords: yeast, aging, mitochondria, mitochondrial lipidome, mitochondrial proteome, Gerotarget
Received: February 20, 2017 Accepted: March 20, 2017 Published: March 31, 2017
Abstract
We have previously found that exogenously added lithocholic acid delays yeast chronological aging. We demonstrated that lithocholic acid enters the yeast cell, is sorted to mitochondria, resides in both mitochondrial membranes, changes the relative concentrations of different membrane phospholipids, triggers changes in the concentrations of many mitochondrial proteins, and alters some key aspects of mitochondrial functionality. We hypothesized that the lithocholic acid-driven changes in mitochondrial lipidome may have a causal role in the remodeling of mitochondrial proteome, which may in turn alter the functional state of mitochondria to create a mitochondrial pattern that delays yeast chronological aging. Here, we test this hypothesis by investigating how the ups1Δ, ups2Δ and psd1Δ mutations that eliminate enzymes involved in mitochondrial phospholipid metabolism influence the mitochondrial lipidome. We also assessed how these mutations affect the mitochondrial proteome, influence mitochondrial functionality and impinge on the efficiency of aging delay by lithocholic acid. Our findings provide evidence that 1) lithocholic acid initially creates a distinct pro-longevity pattern of mitochondrial lipidome by proportionally decreasing phosphatidylethanolamine and cardiolipin concentrations to maintain equimolar concentrations of these phospholipids, and by increasing phosphatidic acid concentration; 2) this pattern of mitochondrial lipidome allows to establish a specific, aging-delaying pattern of mitochondrial proteome; and 3) this pattern of mitochondrial proteome plays an essential role in creating a distinctive, geroprotective pattern of mitochondrial functionality.
Introduction
An age-related deterioration of mitochondrial functionality is the universal hallmark of aging in eukaryotes across phyla [1]. This age-related deterioration is manifested as a progressive decline of the efficiencies with which mitochondria create the bulk of cellular ATP and generate biosynthetic intermediates for amino acids, nucleotides and lipids [1-10].
The functional state of mitochondria defines the pace of the replicative and chronological modes of aging in the yeast Saccharomyces cerevisiae [11-15]. Some traits of mitochondrial functionality are well known for their essential roles in yeast replicative and chronological aging. These mitochondrial traits include the following: 1) electron transport chain, oxidative phosphorylation and membrane potential [11-22]; 2) reactive oxygen species (ROS) homeostasis [11-13, 17, 23-34]; 3) protein synthesis and proteostasis [11, 27, 35-47]; 4) synthesis and assembly of iron-sulfur clusters [19, 27, 48-50]; 5) amino acid synthesis [12, 24, 27, 34, 51-56]; and 6) NADPH synthesis [12, 27, 34, 57, 58].
It remains unknown, however, if such an important trait of mitochondrial functionality as the composition of mitochondrial membrane lipids can play a role in yeast aging. We have previously found that exogenous lithocholic bile acid (LCA) delays the onset and decreases the rate of yeast chronological aging [20, 59]. We showed that the aging-delaying efficiency of LCA under caloric restriction (CR) on 0.2% glucose greatly exceeds its aging-delaying efficiency under non-CR conditions on 2% glucose [20]. We demonstrated that exogenously added LCA enters the yeast cell, accumulates in mitochondria, resides mainly in the inner mitochondrial membrane (IMM), and also associates with the outer mitochondrial membrane (OMM) [60]. We provided evidence that mitochondria-associated LCA alters the abundance and relative concentrations of different classes of membrane phospholipids [60], elicits age-related changes in the concentrations of many mitochondrial proteins [61], and modifies the age-related chronology of some key aspects of mitochondrial functionality [60]. Based on these findings, we proposed the following hypotheses: 1) LCA delays yeast chronological aging because it initially causes specific changes in the composition of mitochondrial membrane lipids; 2) the LCA-driven changes in mitochondrial lipidome then alter mitochondrial proteome; and 3) these changes in protein composition of mitochondria lead to specific alterations in mitochondrial functionality, thus creating a mitochondrial pattern that delays the onset and slows down the progression of yeast chronological aging [61, 62].
In our hypotheses, the LCA-dependent specific changes in the composition of mitochondrial membrane lipids may have a causal role in the age-related remodeling of mitochondrial proteome. The hypotheses further posit that certain mitochondrial proteins whose abundance is altered in response to LCA-driven changes in mitochondrial lipidome may play essential roles in creating a distinct, aging-delaying pattern of mitochondrial functionality. To test our hypotheses, in this study we investigated how the ups1Δ, ups2Δ and psd1Δ mutations eliminating different enzymes involved in mitochondrial phospholipid metabolism influence the following: 1) mitochondrial lipidome and proteome; 2) mitochondrial functionality; and 3) the geroprotective (aging-delaying) efficiency of LCA in chronologically aging yeast. These analyses revealed a distinct LCA-dependent pro-longevity pattern of mitochondrial lipidome, which consists in a proportional decrease of phosphatidylethanolamine and cardiolipin concentrations to maintain equimolar concentrations of these phospholipids, and in an increase of phosphatidic acid concentration. In turn, this pattern of mitochondrial lipidome enables a sustained specific aging-delaying pattern of mitochondrial proteome. Therefore, we also investigated how single-gene-deletion mutations eliminating the key proteins of such mitochondrial proteome pattern affect the efficiency of aging delay by LCA. In all these experiments yeast cells were cultured under CR in medium initially containing 0.2% glucose.
Results
The relative concentrations of mitochondrial membrane phospholipids define the geroprotective (aging-delaying) efficiency of LCA
Our first objective was to test a hypothesis that the composition of mitochondrial membrane lipids may define the efficiency with which LCA delays yeast chronological aging. To attain this objective, we examined how single-gene-deletion mutations eliminating proteins involved in different aspects of phospholipid metabolism and transfer in mitochondrial membranes influence mitochondrial lipidome. We also assessed how these mutations affect the efficiency of yeast chronological aging delay by LCA.
A spatiotemporal dynamics of processes that define the relative concentrations of different classes of membrane phospholipids in yeast mitochondria is well-understood [63-70]. These processes are catalyzed by enzymes that reside in both mitochondria and the endoplasmic reticulum (ER). These processes include the following steps of phospholipid synthesis and transfer: 1) the synthesis of phosphatidic acid (PA), cytidine diphosphate-diacylglycerol (CDP-DAG), diacylglycerol (DAG), phosphatidylserine (PS), phosphatidylcholine (PC) and phosphatidylinositol (PI) in the ER; 2) the movement of PA from the ER to the OMM through mitochondria-ER contact sites at zones of a juxtaposition between the OMM and the mitochondria-associated membrane (MAM) domain of the ER; 3) the transfer of PA from the OMM across the intermembrane space (IMS) to the IMM, which is catalyzed by the Ups1/Mdm35 protein complex and inhibited by CL; 4) the conversion of ER-derived PA into CDP-DAG, phosphatidylglycerol-phosphate (PGP), phosphatidylglycerol (PG), cardiolipin (CL) and monolysocardiolipin (MLCL) in a series of reactions that are catalyzed by Tam41, Pgs1, Gep4, Crd1, Cld1 and Taz1 (respectively) in the IMM; 5) the transfer of PS from the ER to the OMM via mitochondria-ER contact sites by an unidentified mechanism; 6) the Ups2/Mdm35-dependent transport of PS from the OMM via the IMS to the IMM, where PS is converted into phosphatidylethanolamine (PE) in a reaction catalyzed by Psd1; 7) the synthesis of PE from PS in the OMM, which is catalyzed by Psd1, requires a close apposition between the two mitochondrial membranes and is assisted by the mitochondrial contact site (MICOS) protein complex; 8) the transfer of PC and PI from the ER to the OMM via mitochondria-ER contact sites, which is followed by the movement of PC and PI from the OMM to the IMM; mechanisms of both these processes remain obscure; and 9) the movement of DAG and CDP-DAG from the ER to the OMM across mitochondria-ER contact sites, and the subsequent transfer of these two phospholipids to the IMM by currently unknown mechanisms (Figure 1) [63-70].
Figure 1: The relative concentrations of different classes of membrane phospholipids in yeast mitochondria depend on several processes of phospholipid synthesis and transfer. These processes are catalyzed by enzymes that reside in the inner mitochondrial membrane (IMM), intermembrane space (IMS), outer mitochondrial membrane (OMM) and endoplasmic reticulum (ER). Only enzymes catalyzing these processes in the IMM, IMS and OMM are shown. A T bar denotes a cardiolipin (CL)-dependent inhibition of phosphatidic acid (PA) transfer from the OMM across the IMS to the IMM. In this study we investigated various effects of single-gene-deletion mutations that eliminate enzymes displayed in red color. See text for more details. Abbreviations: CDP-DAG, cytidine diphosphate-diacylglycerol; DAG, diacylglycerol; MAM, the mitochondria-associated membrane domain of the ER; MICOS, the mitochondrial contact site protein complex; MLCL, monolysocardiolipin; PC, phosphatidylcholine; PG, phosphatidylglycerol; PGP, phosphatidylglycerol-phosphate; PI, phosphatidylinositol; PS, phosphatidylserine.
The ups1Δ mutation alters mitochondrial membrane lipidome and lowers the geroprotective efficiency of LCA
We used quantitative mass spectrometry to compare lipidomes of mitochondria purified from wild-type (WT) yeast cells cultured with or without LCA to those from ups1Δ cells. Both WT and ups1Δ cells were recovered on day 2, 4 or 7 of cell culturing, i.e. at different stages of chronological aging. The ups1Δ mutation eliminates a component of the Ups1/Mdm35 protein complex, which catalyzes the transfer of PA from the OMM across the IMS to the IMM [63, 71, 72]. We found that 1) akin to the effect of LCA on mitochondrial membrane lipidome in WT, LCA increases the concentrations of PS, PI, PC and PA in mitochondria of ups1Δ in an age-related manner; 2) similar to its effect in WT, LCA decreases the concentration of PE in mitochondrial membranes of ups1Δ at different stages of chronological aging; and 3) unlike an age-related decrease in the concentration of CL elicited by LCA in WT, this bile acid does not cause significant changes in CL concentration in ups1Δ (compare Supplementary Figures S1 and S2).
We then used these data to compare the ratios between concentrations of all possible pairwise combinations of phospholipid classes in mitochondrial membranes of WT and ups1Δ cells cultured with or without LCA. Of note, PA, PE and CL are phospholipid classes that have the non-bilayer forming shape of a cone; they increase the extent of membrane curving for the IMM, thereby raising the abundance of mitochondrial cristae (formed by the IMM) and mitochondrial contact cites (formed between the IMM and OMM) [60, 69, 70, 73-78]. In contrast, PS, PC and PI are phospholipid classes that exhibit the bilayer forming shape of a cylinder; they decrease the extent of membrane curving for the IMM, thus 1) increasing the abundance of the IMM domains having ″flat″ bilayer conformation; 2) decreasing the abundance of the IMM domains exhibiting negative curvature typical of mitochondrial contact sites; and 3) decreasing the abundance of the IMM domains displaying positive curvature characteristic of mitochondrial cristae [60, 69, 70, 73-78]. We found that, in cells cultured with or without LCA, the ups1Δ mutation 1) increases the PA/PS, PA/PC and PA/PI ratios for non-bilayer forming PA vs. bilayer forming PS, PC and PI; 2) does not alter the PE/PS, PE/PC and PE/PI ratios for non-bilayer forming PE vs. PS, PC and PI; 3) decreases the CL/PS, CL/PC and CL/PI ratios for non-bilayer forming CL vs. PS, PC and PI; 4) does not change the PS/PI, PS/PC and PI/PC ratios for all these bilayer forming phospholipid classes; and 5) increases the PA/PE, PA/CL and PE/CL ratios for all these non-bilayer forming phospholipid classes (Figure 2). Thus, while this mutation alters the relative to each other concentrations for all non-bilayer forming phospholipids, it has no effect on the relative to each other concentrations for phospholipids that exhibit the bilayer forming shape.
Figure 2: The ups1Δ mutation differently affects the ratios between concentrations of pairwise combinations of different phospholipid classes in mitochondrial membranes of chronologically aging yeast. ups1Δ cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA or without it. Mitochondria were purified from cells recovered on day 2 A., 4 B. or 7 C. of cell culturing. Extraction of mitochondrial membrane lipids, and mass spectrometric identification and quantitation of the extracted phospholipid classes were carried out as described in Materials and methods. Based on these data, the ratios between concentrations of all possible pairwise combinations of phospholipid classes were calculated. Data are presented as means ± SEM (n = 3; *p < 0.05; ns, not significant).
We then assessed the effect of the ups1Δ mutation on the chronological lifespan (CLS) of yeast cultured with or without LCA. We found that ups1Δ 1) significantly shortens yeast CLS in the absence of LCA (Figures 3A and 3B); and 2) substantially lowers the geroprotective efficiency of LCA by almost completely eliminating the ability of LCA to increase both the mean and the maximum CLS (Figures 3A-3D).
In sum, these findings suggest that the ups1Δ mutation may accelerate yeast chronological aging and decrease the geroprotective efficiency of LCA because it creates a distinct pro-aging pattern of mitochondrial lipidome. This characteristic of ups1Δ pattern may include the following specific changes in the relative concentrations of different classes of membrane phospholipids: 1) an increase of the PA/PS, PA/PC and PA/PI ratios for non-bilayer forming PA vs. bilayer forming PS, PC and PI; 2) a decrease of the CL/PS, CL/PC and CL/PI ratios for non-bilayer forming CL vs. bilayer forming PS, PC and PI; and 3) an increase of the PA/PE, PA/CL and PE/CL ratios for all these non-bilayer forming phospholipid classes (Figure 3E).
Figure 3: The ups1Δ mutation shortens yeast CLS in the absence of LCA and lowers the aging-delaying efficiency of LCA. WT and ups1Δ cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA or without it. A. Survival curves of chronologically aging WT and ups1Δ strains are shown. Data are presented as means ± SEM (n = 3). B. p Values for different pairs of survival curves of WT and ups1Δ strains cultured with or without LCA. Survival curves shown in A. were compared. Two survival curves were considered statistically different if the p value was less than 0.05. The p values for comparing pairs of survival curves using the logrank test were calculated as described in Materials and methods. C. and D. Survival curves shown in A. were used to calculate the percentage of increase of the mean and maximum CLS by LCA for WT and ups1Δ strains. Data are presented as means ± SEM (n = 3; *p < 0.05). E. The pattern of mitochondrial lipidome characteristic of the ups1Δ mutation is shown. Arrows next to the ratios between concentrations of different pairwise combinations of phospholipid classes indicate ratios that are increased (red arrows) or decreased (blue arrows) in ups1Δ cells (as compared to WT cells) cultured with or without LCA. Each colored line connects the names of two phospholipid classes whose concentration ratio is increased (red lines) or decreased (blue lines) by the ups1Δ mutation and cannot be restored by LCA.
The ups2Δ mutation changes the composition of mitochondrial membrane lipids and amplifies the aging-delaying effect of LCA
Using quantitative mass spectrometry, we compared lipidomes of mitochondria purified from WT and ups2Δ cells. Both WT and mutant strains were cultured with or without LCA and recovered on day 2, 4 or 7 of cell culturing. The ups2Δ mutation eliminates a component of the Ups2/Mdm35 protein complex; Ups2/Mdm35 catalyzes the transfer of PS from the OMM across the IMS to the IMM, where PS is converted into PE in a Psd1-dependent reaction [66, 67, 70]. We found that similar to the effect of LCA on mitochondrial membrane lipidome in WT, LCA causes an age-related increase in the concentrations of PS, PI, PC and PA in mitochondria of ups2Δ; however, the concentration of PA in mitochondria of ups2Δ exceeds that in WT mitochondria of cells cultured with or without LCA (compare Supplementary Figures S1 and S3). We also observed that akin to the effect of LCA on mitochondrial membrane lipidome in WT, LCA elicits an age-related decline in the concentrations of PE and CL in mitochondria of ups2Δ; yet, the concentrations of both these phospholipids in mitochondria of ups2Δ are lower than in WT mitochondria of cells cultured with or without LCA (compare Supplementary Figures S1 and S3).
Using the above data, we then compared the ratios between concentrations of all conceivable pairwise combinations of different phospholipids in membranes of mitochondria purified from WT and ups2Δ cells; these cells were cultured with or without LCA. We found that, in cells cultured in the presence or absence of LCA, the ups2Δ mutation 1) raises the PA/PS, PA/PC and PA/PI ratios for non-bilayer forming PA vs. bilayer forming PS, PC and PI; 2) lowers the PE/PS, PE/PC and PE/PI ratios for non-bilayer forming PE vs. PS, PC and PI; 3) lessens the CL/PS, CL/PC and CL/PI ratios for non-bilayer forming CL vs. PS, PC and PI; 4) does not alter the PS/PI, PS/PC and PI/PC ratios for all these bilayer forming classes of phospholipids; 5) rises the PA/PE and PA/CL ratios for all these non-bilayer forming phospholipid classes; and 6) does not alter the PE/CL ratio for these two non-bilayer forming phospholipids (Figure 4). Thus, unlike the ups1Δ mutation, ups2Δ allows to maintain the equimolar concentrations of two non-bilayer forming phospholipids, PE and CL, by proportionally decreasing their concentrations.
Figure 4: The ups2Δ mutation exhibits differential effects on the ratios between concentrations of different pairwise combinations of phospholipid classes in mitochondrial membranes of chronologically aging yeast. ups2Δ cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA or without it. Mitochondria were purified from cells recovered on day 2 A., 4 B. or 7 C. of cell culturing. Extraction of mitochondrial membrane lipids, and mass spectrometric identification and quantitation of the extracted phospholipid classes were carried out as described in Materials and methods. Based on these data, the ratios between concentrations of all possible pairwise combinations of phospholipid classes were calculated. Data are presented as means ± SEM (n = 3; *p < 0.05; ns, not significant).
Our assessment of the effect of the ups2Δ mutation on the CLS of yeast cultured with or without LCA revealed that ups2Δ 1) extends yeast CLS in the absence of LCA (Figures 5A and 5B); and 2) significantly amplifies the geroprotective efficiency of LCA by enhancing the ability of this bile acid to increase both the mean and the maximum CLS (Figures 5A-5D).
Taken together, the above findings indicate that the ups2Δ mutation may slow down yeast chronological aging and increase the geroprotective efficiency of LCA because it establishes a distinctive aging-delaying pattern of mitochondrial lipidome. This ups2Δ-specific pattern may consist of the following distinct changes in the relative concentrations of different phospholipid classes: 1) an increase of the PA/PS, PA/PC and PA/PI ratios for non-bilayer forming PA vs. bilayer forming PS, PC and PI; 2) a decrease of the PE/PS, PE/PC and PE/PI ratios for non-bilayer forming PE vs. bilayer forming PS, PC and PI; 3) a decline of the CL/PS, CL/PC and CL/PI ratios for non-bilayer forming CL vs. bilayer forming PS, PC and PI; and 4) a rise of the PA/PE and PA/CL ratios for these non-bilayer forming classes of phospholipids (Figure 5E).
Figure 5: The ups2Δ mutation extends yeast CLS in the absence of LCA and amplifies the geroprotective efficiency of LCA. WT and ups2Δ cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA or without it. A. Survival curves of chronologically aging WT and ups2Δ strains are shown. Data are presented as means ± SEM (n = 3). B. p Values for different pairs of survival curves of WT and ups2Δ strains cultured with or without LCA. Survival curves shown in A. were compared. Two survival curves were considered statistically different if the p value was less than 0.05. The p values for comparing pairs of survival curves using the logrank test were calculated as described in Materials and methods. C. and D. Survival curves shown in A. were used to calculate the percentage of increase of the mean and maximum CLS by LCA for WT and ups2Δ strains. Data are presented as means ± SEM (n = 3; *p < 0.05). E. The pattern of mitochondrial lipidome characteristic of the ups2Δ mutation is shown. Arrows next to the ratios between concentrations of different pairwise combinations of phospholipid classes indicate ratios that are increased (red arrows) or decreased (blue arrows) in ups2Δ cells (as compared to WT cells) cultured with or without LCA. Each colored line connects the names of two phospholipid classes whose concentration ratio is increased (red lines) or decreased (blue lines) by the ups2Δ mutation and cannot be restored by LCA.
The psd1Δ mutation elicits changes in mitochondrial membrane lipidome and lessens the geroprotective efficiency of LCA
We compared lipidomes of purified mitochondria from WT cells cultured with or without LCA to those from psd1Δ cells. These cells were recovered for purification of mitochondria on day 2, 4 or 7 of cell culturing. The psd1Δ mutation eliminates phosphatidylserine decarboxylase which catalyzes the conversion of PS to PE in the IMM and OMM [66, 67, 70, 79, 80]. We found that similar to the effect of LCA on mitochondrial membrane lipidome in WT, LCA causes an age-related rise in the concentrations of PS, PI, PC and PA in mitochondria of psd1Δ; however, the concentration of PA in mitochondria of psd1Δ is higher than in mitochondria of WT cultured with or without LCA (compare Supplementary Figures S1 and S4). We also observed that akin to the effect of LCA on mitochondrial membrane lipidome in WT, LCA triggers an age-related decline in the concentrations of PE and CL in mitochondria of psd1Δ; however, the concentrations of both PE and CL in mitochondria of psd1Δ are lower than in mitochondria of WT cultured with or without LCA (compare Supplementary Figures S1 and S4).
We then used the above data to compare the ratios between concentrations of all possible pairwise combinations of phospholipid classes in mitochondrial membranes of WT and psd1Δ cells cultured in the presence or absence of LCA. We found that, in cells cultured with or without LCA, the psd1Δ mutation 1) augments the PA/PS, PA/PC and PA/PI ratios for non-bilayer forming PA vs. bilayer forming PS, PC and PI; 2) reduces the PE/PS, PE/PC and PE/PI ratios for non-bilayer forming PE vs. PS, PC and PI; 3) lessens the CL/PS, CL/PC and CL/PI ratios for non-bilayer forming CL vs. PS, PC and PI; 4) does not change the PS/PI, PS/PC and PI/PC ratios for all these bilayer forming classes of phospholipids; 5) rises the PA/PE and PA/CL ratios for all these non-bilayer forming phospholipid classes; and 6) decreases the PE/CL ratio for these two non-bilayer forming phospholipids (Figure 6). Thus, unlike ups2Δ and similar to ups1Δ, the psd1Δ mutation does not allow to maintain the equimolar concentrations of two non-bilayer forming phospholipids, PE and CL.
Our assessment of how the psd1Δ mutation influences the CLS of yeast cultured with or without LCA showed that psd1Δ 1) shortens yeast CLS in the absence of LCA (Figures 7A and 7B); and 2) substantially decreases the aging-delaying efficiency of LCA by significantly lowering the ability of this bile acid to increase both the mean and the maximum CLS (Figures 7A-7D).
Collectively, these findings suggest that the psd1Δ mutation may accelerate yeast chronological aging and decrease the geroprotective efficiency of LCA because it establishes a distinct pro-aging pattern of mitochondrial lipidome. This characteristic for psd1Δ pattern may include the following specific changes in the relative concentrations of different classes of membrane phospholipids: 1) an increase of the PA/PS, PA/PC and PA/PI ratios for non-bilayer forming PA vs. bilayer forming PS, PC and PI; 2) a decrease of the PE/PS, PE/PC and PE/PI ratios for non-bilayer forming PE vs. bilayer forming PS, PC and PI; 3) a decline of the CL/PS, CL/PC and CL/PI ratios for non-bilayer forming CL vs. bilayer forming PS, PC and PI; 4) an increase of the PA/PE and PA/CL ratios for these non-bilayer forming phospholipid classes; and 5) a decrease in the PE/CL ratio for these two non-bilayer forming classes of phospholipids (Figure 7E).
A distinct pro-longevity pattern of mitochondrial lipidome extends yeast CLS in the absence of LCA and amplifies the geroprotective efficiency of LCA
We noticed that the ups1Δ, ups2Δ and psd1Δ mutations cause some similar changes to the ratios between concentrations of various pairwise combinations of mitochondrial membrane phospholipids (compare Figures 3E, 5E and 7E). We therefore compared the datasets of such ratios that have been statistically significantly changed (SSC) by the ups1Δ, ups2Δ and psd1Δ mutations in yeast cultured with or without LCA. We found the following for the total of 12 SSC ratios: 1) 8 SSC ratios overlap between the ups1Δ, ups2Δ and psd1Δ datasets; 2) 3 SSC ratios are common to the datasets of the CLS-extending ups2Δ mutation that amplifies the geroprotective efficiency of LCA and the CLS-shortening psd1Δ mutation that lessens such efficiency; and 3) 1 SSC ratio, namely PE/CL, is common to the datasets of the ups1Δ and psd1Δ mutations, both of which are CLS-shortening mutations that lower the geroprotective efficiency of LCA (ups1Δ increases the PE/CL ratio, whereas psd1Δ decreases it) (Figure 8A).
We also noticed that some ratios between concentrations of various pairwise combinations of mitochondrial membrane phospholipids are not statistically changed by the ups1Δ, ups2Δ and psd1Δ mutations. Our analysis of these statistically unchanged (SU) ratios revealed the following: 1) 3 SU ratios overlap between the ups1Δ, ups2Δ and psd1Δ datasets; 2) 3 SU ratios are unique to the dataset of ups1Δ, a CLS-shortening mutation that lowers the geroprotective efficiency of LCA; and 3) 1 SU ratio, namely PE/CL, is unique to the dataset of ups2Δ, a CLS-extending mutation that amplifies the geroprotective efficiency of LCA (Figure 8B).
In sum, these findings suggest that the maintenance of equimolar concentrations of two non-bilayer forming and cone-shaped phospholipids, PE and CL, may be critical feature of the pro-longevity pattern of mitochondrial lipidome (Figure 8C). This feature is a longevity assurance trait in the absence of LCA. This feature is also required for the delay of yeast chronological aging by exogenous LCA.
The maintenance of equimolar concentrations of PE and CL is a trait that is common to WT and ups2Δ, a mutant strain that not only lives longer than WT but also exhibits an amplified (as compared to WT) geroprotective efficiency of LCA (Figure 5). It is conceivable, therefore, that some traits distinguishing mitochondrial lipidome of ups2Δ from that of WT may represent additional features of the pro-longevity pattern of mitochondrial lipidome. These additional features are likely to be responsible for the ability of the ups2Δ mutation to extend longevity in the absence of LCA and also to increase the geroprotective efficiency of LCA. Among these additional features are the ones that differentiate mitochondrial lipidome of ups2Δ from that of WT; they include the following: 1) an increased concentration of PA, another non-bilayer forming and cone-shaped phospholipid; 2) a decreased concentration of PE; and 3) a proportionally (as compared to PE) decreased concentration of CL (compare Supplementary Figures S1 and S3). We hypothesize that the proportional decrease in the concentrations of PE and CL in mitochondrial membranes of ups2Δ may be responsible for the increased concentration of PA in these membranes.
The ups1Δ and ups2Δ mutations alter the concentrations of many mitochondrial proteins in yeast cultured with or without LCA
Our hypothesis posits that the LCA-dependent establishment and maintenance of a distinct pro-longevity pattern of mitochondrial lipidome may have a causal role in the age-related remodeling of mitochondrial proteome. We therefore used quantitative mass spectrometry to compare the identities and relative concentrations of proteins that were recovered in mitochondria purified from WT, ups1Δ and ups2Δ cells cultured with or without LCA. The ups1Δ mutation establishes and maintains a distinct pro-aging pattern of mitochondrial lipidome (Figures 2, 3 and 8), shortens CLS (Figure 3), and lowers the geroprotective efficiency of LCA (Figure 3). In contrast, the ups2Δ mutation institutes and preserves a specific pro-longevity pattern of mitochondrial lipidome (Figures 4, 5 and 8), extends CLS (Figure 5), and amplifies the geroprotective efficiency of LCA (Figure 5).
We found that both mutations, ups1Δ and ups2Δ, alter the age-related chronology of changes in concentrations of numerous mitochondrial proteins in yeast cultured in the presence of LCA or in its absence; these proteins have been implicated in many essential mitochondrial functions (see Supplementary Figure S5 and Supplementary Tables S1 - S9 for ups1Δ, and Supplementary Figure S7 and Supplementary Tables S10 - S15 for ups2Δ).
We then compared the datasets of relative concentrations of mitochondrial proteins that are statistically significantly downregulated or upregulated 1) by LCA in WT; 2) by the ups1Δ or ups2Δ mutation in the absence of LCA; and 3) by LCA in ups1Δ or ups2Δ cells.
Our comparative analysis of these datasets for ups1Δ revealed the following: 1) many mitochondrial proteins that are downregulated or upregulated in ups1Δ cells cultured without LCA are unique to these datasets (i.e. these proteins are not present in the datasets of mitochondrial proteins that are downregulated or upregulated by LCA in WT or by LCA in ups1Δ cells) (Supplementary Figures S6A - S6F); and 2) the total number and identities of mitochondrial proteins that are downregulated or upregulated in ups1Δ cells cultured with or without LCA fluctuate significantly in cells recovered on day 2, 4 or 7 of cell culturing (i.e. at different stages of chronological aging) (Supplementary Figures S6H - S6L).
For ups2Δ, we found that: 1) a number of mitochondrial proteins that are downregulated or upregulated in ups2Δ cells cultured in the absence of LCA cannot be found in the datasets of mitochondrial proteins downregulated or upregulated by LCA in WT or by LCA in ups2Δ cells (Supplementary Figures S8A - S8F); 2) the total number and identities of mitochondrial proteins that are downregulated or upregulated in ups2Δ cells cultured in the absence of LCA vary substantially with the chronological age of cells (Supplementary Figures S8H and S8K); 3) numerous mitochondrial proteins that are downregulated or upregulated by LCA in ups2Δ cells are unique to these datasets as they cannot be found in the datasets of mitochondrial proteins downregulated or upregulated by LCA in WT or by the ups2Δ mutation in the absence of LCA (Supplementary Figures S8A - S8F); and 4) the total number and identities of mitochondrial proteins that are downregulated or upregulated by LCA in ups2Δ cells fluctuate significantly with the chronological age of cells (Supplementary Figures S8I and S8L).
Taken together, these findings indicate that in yeast cultured with or without LCA 1) the establishment and maintenance of a distinct pro-aging pattern of mitochondrial lipidome in short-lived ups1Δ cells (Figures 2, 3 and 8) correlate with the establishment and maintenance of a specific aging-accelerating pattern of mitochondrial proteome in these mutant cells; and 2) the institution and preservation of a specific pro-longevity pattern of mitochondrial lipidome in long-lived ups2Δ cells (Figures 4, 5 and 8) correlate with the institution and preservation of a distinctive aging-delaying pattern of mitochondrial proteome in these mutant cells.
Figure 6: The psd1Δ mutation differently affects the ratios between concentrations of pairwise combinations of different phospholipid classes in mitochondrial membranes of chronologically aging yeast. psd1Δ cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA or without it. Mitochondria were purified from cells recovered on day 2 A., 4 B. or 7 C. of cell culturing. Extraction of mitochondrial membrane lipids, and mass spectrometric identification and quantitation of the extracted phospholipid classes were carried out as described in Materials and methods. Based on these data, the ratios between concentrations of all possible pairwise combinations of phospholipid classes were calculated. Data are presented as means ± SEM (n = 3; *p < 0.05; ns, not significant).
Figure 7: The psd1Δ mutation shortens yeast CLS in the absence of LCA and considerably decreases the geroprotective efficiency of LCA. WT and psd1Δ cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA or without it. A. Survival curves of chronologically aging WT and psd1Δ strains are shown. Data are presented as means ± SEM (n = 3). B. p Values for different pairs of survival curves of WT and psd1Δ strains cultured with or without LCA. Survival curves shown in A. were compared. Two survival curves were considered statistically different if the p value was less than 0.05. The p values for comparing pairs of survival curves using the logrank test were calculated as described in Materials and methods. C. and D. Survival curves shown in A. were used to calculate the percentage of increase of the mean and maximum CLS by LCA for WT and psd1Δ strains. Data are presented as means ± SEM (n = 3; *p < 0.05). E. The pattern of mitochondrial lipidome characteristic of the psd1Δ mutation is shown. Arrows next to the ratios between concentrations of different pairwise combinations of phospholipid classes indicate ratios that are increased (red arrows) or decreased (blue arrows) in psd1Δ cells (as compared to WT cells) cultured with or without LCA. Each colored line connects the names of two phospholipid classes whose concentration ratio is increased (red lines) or decreased (blue lines) by the psd1Δ mutation and cannot be restored by LCA.
Figure 8: Venn diagrams showing a comparison of the effects of the ups1Δ, ups2Δ and psd1Δ mutations on the ratios between concentrations of various pairwise combinations of mitochondrial membrane phospholipids. A comparison of the datasets for the ratios that have been statistically significantly changed A. or statistically unchanged B. by the ups1Δ, ups2Δ and psd1Δ mutations in yeast cultured with or without LCA are shown. C. The maintenance of equimolar concentrations of PE and CL is an essential feature of the pro-longevity pattern of mitochondrial lipidome. Arrows next to the ratios between concentrations of different pairwise combinations of phospholipid classes indicate ratios that are increased (red arrows) or decreased (blue arrows) in ups1Δ, ups2Δ or psd1Δ cells (as compared to WT cells) cultured with or without LCA.
The mitochondrial proteomes of ups1Δ and ups2Δ differ substantially
Because our findings suggest that in yeast cultured with or without LCA the ups1Δ and ups2Δ mutations can establish and maintain either an aging-accelerating or an aging-delaying (respectively) pattern of mitochondrial proteome, we compared the datasets of relative concentrations of mitochondrial proteins that are statistically significantly downregulated or upregulated in ups1Δ or ups2Δ cells in the absence or presence of LCA.
For ups1Δ and ups2Δ cells cultured without LCA, we found the following: 1) many mitochondrial proteins that are downregulated or upregulated in long-lived ups2Δ cells are not present in the datasets of mitochondrial proteins that are downregulated or upregulated in short-lived ups1Δ cells (Figures 9A - 9F; Supplementary Tables S16 and S17); and 2) the total number and identities of mitochondrial proteins that are downregulated or upregulated only in long-lived ups2Δ cells fluctuate significantly in cells recovered at different stages of chronological aging (Figures 9A - 9F; Supplementary Tables S16 and S17). Functions of some mitochondrial proteins that are downregulated or upregulated only in long-lived ups2Δ cells remain to be established (Figures 9G - 9L; Supplementary Tables S16 and S17). Many mitochondrial proteins that are downregulated or upregulated only in long-lived ups2Δ cells have been implicated in essential mitochondrial functions, including the electron transport chain (ETC), respiration, the tricarboxylic acid (TCA) cycle, ribosome assembly, amino acid metabolism, carbohydrate metabolism, protein import, proteostasis, metabolite synthesis, protein synthesis, ATP synthesis, metabolite transport, lipid metabolism, contact sites and cristae maintenance, redox homeostasis, mitochondrial DNA (mtDNA) maintenance, stress response, mRNA synthesis and processing, the maintenance of contact sites between mitochondria and vacuoles, and mitochondrial fusion (Figures 9G - 9L; Supplementary Tables S16 and S17).
Figure 9: In cells cultured without LCA, many mitochondrial proteins that are downregulated or upregulated in long-lived ups2Δ cells are not downregulated or upregulated in short-lived ups1Δ cells. (A - F) Venn diagrams showing a comparison of the datasets of relative concentrations of mitochondrial proteins that are statistically significantly downregulated or upregulated in ups1Δ or ups2Δ cells cultured in the absence of LCA; cells were recovered on day 2, 4 or 7 of culturing. (G - L) Mitochondrial proteins that are downregulated or upregulated only in long-lived ups2Δ cells belong to various functional categories. The names of functional categories whose protein representatives were downregulated or upregulated in ups2Δ cells recovered on every of the three days are underlined. Functions of some mitochondrial proteins that are downregulated or upregulated only in ups2Δ cells are currently unknown. Abbreviations: ETC, electron transport chain; mtDNA, mitochondrial DNA; TCA, the tricarboxylic acid cycle.
For ups1Δ and ups2Δ cells cultured with LCA, we found the following: 1) a number of mitochondrial proteins that are downregulated or upregulated by LCA in long-lived ups2Δ cells cannot be found in the datasets of mitochondrial proteins that are downregulated or upregulated by LCA in WT or short-lived ups1Δ cells (Figures 10A - 10F; Supplementary Tables S18 and S19); and 2) the total number and identities of mitochondrial proteins that are downregulated or upregulated by LCA only in long-lived ups2Δ cells vary notably in cells recovered at different stages of chronological aging (Figures 10A - 10F; Supplementary Tables S18 and S19). Functions of some mitochondrial proteins that are downregulated or upregulated by LCA only in long-lived ups2Δ cells remain unknown (Figures 10G - 10L; Supplementary Tables S18 and S19). Numerous mitochondrial proteins that are downregulated or upregulated by LCA only in long-lived ups2Δ cells are known for their essential roles in the same set of mitochondrial functions as the ones played by proteins that are downregulated or upregulated only in long-lived ups2Δ cells culture without LCA (compare Figures 9G - 9L and Supplementary Tables S16 and S17 to Figures 10G - 10L and Supplementary Tables S18 and S19).
In sum, these findings suggest that in yeast cultured with or without LCA the ups2Δ mutation may establish and maintain an aging-delaying pattern of mitochondrial proteome.
Figure 10: In cells cultured with LCA, many mitochondrial proteins that are downregulated or upregulated by LCA in long-lived ups2Δ cells are not downregulated or upregulated by LCA in WT or short-lived ups1Δ cells. A. - F. Venn diagrams showing a comparison of the datasets of relative concentrations of mitochondrial proteins that are statistically significantly downregulated or upregulated by LCA in WT, ups1Δ or ups2Δ; cells were recovered on day 2, 4 or 7 of culturing. G. - L. Mitochondrial proteins that are downregulated or upregulated by LCA only in long-lived ups2Δ cells belong to many different functional categories. The names of functional categories whose protein representatives were downregulated or upregulated by LCA in ups2Δ cells recovered on every of the three days are underlined. Functions of some mitochondrial proteins that are downregulated or upregulated by LCA only in ups2Δ cells are currently unknown. Abbreviations: ETC, electron transport chain; mtDNA, mitochondrial DNA; TCA, the tricarboxylic acid cycle.
Many mitochondrial proteins that are downregulated or upregulated by LCA only in long-lived ups2Δ cells play essential roles in aging delay by LCA
Because our findings suggest that in yeast cultured with LCA the ups2Δ mutation may establish and maintain a distinct pattern of mitochondrial proteome that is essential for the ability of LCA to delay aging, we investigated how single-gene-deletion mutations eliminating the key proteins constituting such pattern affect the geroprotective efficiency of LCA.
We thought that some of the proteins downregulated by LCA in ups2Δ may function in attenuating the geroprotective efficiency of LCA, and thus the elimination of these proteins by mutations may increase such efficiency. We also thought that some of the proteins upregulated by LCA in ups2Δ may act as facilitators of aging delay by LCA, and therefore the elimination of these proteins by mutations may decrease the geroprotective efficiency of LCA.
We found that mutants that lack 10 out of 12 proteins most highly downregulated by LCA in ups2Δ exhibit a statistically significantly increase of the aging-delaying efficiency of LCA; a slight increase of such efficiency seen in mutants that lack 2 other downregulated by LCA proteins was not statistically significant (Figures 11A - 11C). We also found that mutants that lack 11 out of 12 proteins vastly upregulated by LCA in ups2Δ display a statistically significantly decrease of the geroprotective efficiency of LCA; a minor decrease of such efficiency observed in a mutant lacking one of the downregulated by LCA proteins was not statistically significant (Figures 11D - 11F). Of note, none of these mutants exhibits such robust change of the aging-delaying efficiency of LCA as the changes seen in the ups1Δ, ups2Δ and psd1Δ mutants (compare Figures 3, 5, 7 and 11). This finding suggests that Ups1, Ups2 and Psd1 may function as upstream regulators of various mitochondrial processes whose synergistic action defines the efficiency of aging delay by LCA.
Taken together, these findings further support the notion that the ups2Δ mutation may allow to sustain a distinct aging-delaying pattern of mitochondrial proteome that is essential for the ability of LCA to delay aging.
Figure 11: Many mutations eliminating proteins downregulated by LCA in ups2Δ increase the aging-delaying efficiency of LCA, while many mutations eliminating proteins upregulated by LCA in ups2Δ decrease such efficiency. WT and mutant cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA. A. - C. Survival curves of chronologically aging WT and mutant strains that lack proteins most highly downregulated by LCA in ups2Δ are shown. Data are presented as means ± SEM (n = 3). Also shown are p values for different pairs of survival curves of WT and mutant strains cultured with LCA. Survival curves shown in A. - C. were compared. Two survival curves were considered statistically different if the p value was less than 0.05. The p values for comparing pairs of survival curves using the logrank test were calculated as described in Materials and methods. D. - F. Survival curves of chronologically aging WT and mutant strains that lack proteins most substantially upregulated by LCA in ups2Δ are shown. Data are presented as means ± SEM (n = 3). Also shown are p values for different pairs of survival curves of WT and mutant strains cultured with LCA. Survival curves shown in D. -F. were compared. Two survival curves were considered statistically different if the p value was less than 0.05. The p values for comparing pairs of survival curves using the logrank test were calculated as described in Materials and methods.
The ups1Δ and ups2Δ mutations have different effects on some key aspects of mitochondrial functionality in yeast cultured with LCA
Our hypothesis posits that the LCA-dependent remodeling of mitochondrial lipidome and the resulting changes in mitochondrial proteome may create an aging-delaying pattern of mitochondrial functionality that is essential for the ability of LCA to delay aging. To test this hypothesis, we monitored the age-related chronology of changes in four vital cellular processes confined to and regulated by mitochondria. These processes include the following: 1) mitochondrial respiration; 2) the maintenance of electrochemical potential (ΔΨ) across the IMM; 3) the maintenance of the homeostasis of cellular ROS known to be produced primarily as by-products of mitochondrial respiration [81, 82]; and 4) the modulation of cellular concentrations of ATP, which in yeast cultured in media with low (0.2%) glucose concentration is generated mainly in mitochondria [81, 82]. These vital processes were monitored in chronologically aging WT, ups1Δ and ups2Δ cells cultured with LCA.
We found that in WT cells cultured with LCA the rate of mitochondrial respiration 1) is increased when cells enter diauxic (D) growth phase that begins on day 2 of culturing; 2) reaches a plateau in post-diauxic (PD) growth phase that occurs between days 3 and 7 of culturing; and 3) slightly declines during the subsequent stationary (ST) growth phase that follows PD phase and begins after day 7 of culturing (Figure 12A). In ups2Δ cells cultured with LCA the rate of mitochondrial respiration 1) is increased to a significantly higher extent during D phase than in WT cells; and 2) reaches a plateau in PD phase and then additionally rises in ST phase to a substantially higher level than that in WT cells (Figure 12A). In ups1Δ cells cultured with LCA the rate of mitochondrial respiration 1) is increased to a significantly lower degree during D phase than in WT cells; and 2) substantially declines in PD and ST phases to reach a markedly lower level than that in WT cells (Figure 12A).
In WT cells cultured with LCA the value of ΔΨ 1) is increased during D phase; 2) reaches a plateau during PD phase; and 3) slightly rises during ST phase (Figure 12B). In ups2Δ cells cultured with LCA the value of ΔΨ 1) is increased to a similar extent during D phase as in WT cells; 2) further rises during PD phase to reach a level significantly exceeding that in WT cells; and 3) slightly declines but remains higher than that in WT cells during ST phase (Figure 12B). In ups1Δ cells cultured with LCA the value of ΔΨ 1) is increased to a significantly lower degree during D phase than in WT cells; and 2) slightly rises during PD phase and then declines in ST phase to reach a substantially lower level than that in WT cells (Figure 12B).
In WT cells cultured with LCA the concentration of ROS 1) is increased during D phase; 2) reaches a plateau during PD phase; and 3) remains mainly unchanged during ST phase (Figure 12C). In ups2Δ cells cultured with LCA the concentration of ROS 1) is increased to a lower degree during D phase than in WT cells; and 2) undergoes minor changes during PD and ST phases to reach a level that is significantly lower than that in WT cells (Figure 12C). In ups1Δ cells cultured with LCA the concentration of ROS 1) is increased to a similar extent during D phase as in WT cells; and 2) further rises during PD and ST phases to reach a level significantly exceeding that in WT cells (Figure 12C).
In WT cells cultured with LCA the concentration of ATP 1) is increased during D phase; 2) reaches a plateau during PD phase; and 3) slightly declines during ST phase (Figure 12D). In ups2Δ cells cultured with LCA the concentration of ATP 1) is increased to a similar degree during D phase as in WT cells; 2) further rises during PD phase to reach a level significantly higher than that in WT cells; and 3) slightly declines but remains higher than that in WT cells during ST phase (Figure 12D). In ups1Δ cells cultured with LCA the value of ΔΨ 1) is increased to a significantly lower extent during D phase than in WT cells; and 2) remains unchanged during PD phase and then declines in ST phase to reach a substantially lower level than that in WT cells (Figure 12D).
In sum, these findings support the notion that the LCA-dependent remodeling of mitochondrial lipidome and the resulting changes in mitochondrial proteome can create an aging-delaying pattern of mitochondrial functionality that is essential for the ability of LCA to delay aging.
Figure 12: In yeast cultured with LCA, the ups1Δ and ups2Δ mutations differently affect four key aspects of mitochondrial functionality. WT and mutant cells were cultured in the nutrient-rich YP medium initially containing 0.2% glucose with 50 µM LCA. The dynamics of age-related changes in the rate of oxygen consumption my cells A., electrochemical potential (ΔΨ) across the IMM B., cellular concentration of ROS C. and cellular concentration of ATP D. during chronological aging of yeast. Data are presented as means ± SEM (n = 3; *p < 0.05; **p < 0.01; ***p < 0.001).
Discussion
This study provides evidence that the mitochondrial lipidome defines not only the rate of yeast chronological aging but also the geroprotective efficiency of LCA in chronologically aging yeast. We demonstrate the existence of a distinct pro-longevity pattern of mitochondrial lipidome, which extends yeast CLS in the absence of LCA and amplifies the geroprotective efficiency of LCA. This pattern consists in a proportional decrease of PE and CL concentrations, and in a concomitant increase of PA concentration. PE, CL and PA are non-bilayer forming, cone-shaped phospholipid classes that increase the extent of membrane curving for the IMM to rise the abundance of mitochondrial cristae (formed by the IMM) and mitochondrial contact cites (formed between the IMM and OMM) [60, 69, 70, 73-78]. We also show that these LCA-driven specific changes in the composition of mitochondrial membrane lipids cause a distinct remodeling of mitochondrial proteome by decreasing and increasing concentration of many mitochondrial proteins. These proteins have been implicated in such vital mitochondrial functions as the ETC and respiration, the TCA cycle, ribosome assembly, amino acid metabolism, carbohydrate metabolism, protein import, proteostasis, metabolite synthesis, protein synthesis, ATP synthesis, metabolite transport, lipid metabolism, contact sites and cristae maintenance, redox homeostasis, mtDNA maintenance, stress response, mRNA synthesis and processing, the maintenance of contact sites between mitochondria and vacuoles, and mitochondrial fusion. We provide evidence that the LCA-dependent remodeling of mitochondrial lipidome and the resulting changes in mitochondrial proteome allow to change the age-related chronology of changes in such vital mitochondrial processes as respiration, electrochemical potential maintenance, ROS homeostasis preservation and ATP synthesis. These changes facilitate the establishment and maintenance of an aging-delaying pattern of mitochondrial functionality that is essential for the ability of LCA to delay aging.
The challenge for the future is to define molecular mechanisms underlying the LCA-driven remodeling of mitochondrial lipidome and proteome. Our previous findings suggested a hypothesis in which LCA may cause such remodeling of mitochondrial lipidome by 1) slowing down the Psd1-dependent reaction of the synthesis of PE from PS in the IMM and/or OMM; 2) decelerating the Crd1-dependent reaction of CL synthesis from PG in the IMM; and 3) attenuating a negative feedback loop that involves a CL-dependent inhibition of PA transport from the OMM across the IMS to the IMM, which is catalyzed by the Ups1/Mdm35 protein complex (Figure 1) [60]. Studies aimed at testing this hypothesis are currently in progress. Furthermore, we previously demonstrated that LCA causes major changes not only in mitochondrial membrane lipidome but also in the size, number and morphology of mitochondria [60]. One could envision that these LCA-driven changes in mitochondrial abundance and morphology may affect mitochondrial protein import, folding, assembly and other aspects of mitochondrial proteostasis, thereby altering mitochondrial proteome. Our ongoing studies address the validity of this assumption.
Materials and methods
Yeast strains and growth conditions
The WT strain BY4742 (MATα his3Δ1 leu2Δ0 lys2Δ0 ura3Δ0) and single-gene-deletion mutant strains in the BY4742 genetic background (all from Thermo Scientific/Open Biosystems) were grown in YP medium (1% yeast extract, 2% peptone) initially containing 0.2% glucose with 50 µM LCA or without it. Cells were cultured at 30oC with rotational shaking at 200 rpm in Erlenmeyer flasks at a ʺflask volume/medium volumeʺ ratio of 5:1.
Miscellaneous procedures
Purification of mitochondria [83], SDS-PAGE [84], quantitative mass spectrometric analysis of lipids [85] and statistical analysis [86] were performed as previously described. Mass spectrometric identification and quantification of proteins were performed as previously reported [87]. The ″Proteome Discoverer″ software was used to calculate the exponentially modified protein abundance index (emPAI), a measure of the relative abundance of mitochondrial proteins in a pair of analyzed datasets.
Abbreviations
CL, cardiolipin; CLS, chronological life span; CDP-DAG, cytidine diphosphate-diacylglycerol; DAG, diacylglycerol; D, diauxic; IMM, the inner mitochondrial membrane; IMS, the intermembrane space; LCA, lithocholic bile acid; MAM, mitochondria-associated membrane; MICOS, mitochondrial contact site; MLCL, monolysocardiolipin; OMM, the outer mitochondrial membrane; PA, phosphatidic acid; PC, phosphatidylcholine; PD, post-diauxic; PG, phosphatidylglycerol; PGP, phosphatidylglycerol-phosphate; PI, phosphatidylinositol; PS, phosphatidylserine; ROS, reactive oxygen species; SSC, statistically significantly changed; ST, stationary; SU, statistically unchanged; WT, wild-type.
Author contributions
VIT designed and supervised the study. AL, AA-C, SDB, OK, PK, PD, MA, YM, KM and TDM performed experiments and analyzed the data. AL, AA-C and VIT wrote the manuscript. All authors read the final version of the manuscript.
Acknowledgments
We are grateful to current and former members of the Titorenko laboratory for discussions. We acknowledge the Centre for Biological Applications of Mass Spectrometry and the Centre for Structural and Functional Genomics, both at Concordia University, for outstanding services.
Conflicts of interest
The authors of this manuscript have no conflict of interest to declare.
Funding
This study was supported by grants from the Natural Sciences and Engineering Research Council (NSERC) of Canada and Concordia University Chair Fund. A.A-C. and A.L. were supported by the NSERC Postgraduate Doctoral Scholarship Awards. P.K. was supported by the Fonds québécois de la recherche sur la nature et les technologies Doctoral Research Fellowship Award. P.D. was supported by the Concordia University Graduate Fellowship Award. K.M. was supported by the Concordia University Armand C. Archambault Fellowship and the Concordia University Dean of Arts and Sciences Award of Excellence. V.I.T. is a Concordia University Research Chair in Genomics, Cell Biology and Aging.
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