Oncotarget

Research Papers:

Genome-wide analysis and functional prediction of long non-coding RNAs in mouse uterus during the implantation window

Qi Wang, Nan Wang, Rui Cai, Fan Zhao, Yongjie Xiong, Xiao Li, Aihua Wang, Pengfei Lin _ and Yaping Jin

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Oncotarget. 2017; 8:84360-84372. https://doi.org/10.18632/oncotarget.21031

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Abstract

Qi Wang1,2, Nan Wang1,2, Rui Cai1,2, Fan Zhao1,2, Yongjie Xiong1,2, Xiao Li1,2, Aihua Wang1,2, Pengfei Lin1,2 and Yaping Jin1,2

1College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China

2Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University, Yangling, Shaanxi, China

Correspondence to:

Pengfei Lin, email: [email protected]

Yaping Jin, email: [email protected]

Keywords: long non-coding RNAs, RNA-seq, implantation, uterus, mouse

Received: May 13, 2017     Accepted: August 06, 2017     Published: September 16, 2017

ABSTRACT

Establishment of the receptive uterus is a crucial step for embryo implantation. In this study, the expression profiles and characterization of long non-coding RNAs (lncRNAs) in pregnant mouse uteri on day 4, day 5 at implantation sites and inter-implantation sites were conducted using RNA-seq. A total of 7,764 putative lncRNA transcripts were identified, including 6,179 known lncRNA transcripts and 1,585 novel lncRNA transcripts. Bioinformatics analysis of the cis and trans lncRNA targets showed that the differentially expressed lncRNAs were mainly involved in tissue remodelling, immune response and metabolism-related processes, indicating that lncRNAs could be involved in the regulation of embryo implantation. We also discovered that differentially expressed lncRNAs might regulate multiple signalling pathways that play an important role in the regulation of embryo implantation. In addition, nine known lncRNAs and four novel lncRNAs were randomly selected and validated by qRT-PCR. The expression of Tug1, Neat1, Gas5, Malat1, H19 and Rmst were significantly regulated in the mouse uterus during the implantation window. Our results are the first to systematically identify lncRNAs in the mouse uterus and provide a catalogue of lncRNAs for further understanding their functions in pregnant mouse uteri during the implantation window.


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