Corrections:

Xinpei Yu^1,5,8,9, Junkui Ai¹, Liquan Cai¹, Yifeng Jing^1,6, Dan Wang¹, Jun Dong¹, Laura E. Pascal¹, Jian Zhang⁷, Rongcheng Luo⁸, Zhou Wang^1,2,3,4

¹ Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, USA
² Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, USA
³ Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, USA
⁴ University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, USA
⁵ Department of Geriatrics, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou, China
⁶ Department of Urology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
⁷ Center for Translational Medicine, Guangxi Medical University, Nanning, Guangxi, China
⁸ Cancer Center, Traditional Chinese Medicine-Integrated Hospital, Southern Medical University, Guangzhou, China
⁹ Guangdong Provincial Key Laboratory of Geriatric Infection and Organ Function Support and Guangzhou Key Laboratory of Geriatric Infection and Organ Function Support, Guangzhou, China

Published: December 24, 2019

This article has been corrected: Due to errors during image assembly, the RFP-ELL1 merged image in Figure 4B is incorrect. The proper Figure 4 is shown below. The authors declare that these corrections do not change the results or conclusions of this paper.

Original article: Oncotarget. 2016; 7:29245–29254. DOI: https://doi.org/10.18632/oncotarget.8588.

Figure 4: Mutant EAF2^{K39-81-85-111R} binding and co-localization with ELL1. (A) HEK 293 cells were transfected with myc-EAF2, myc-EAF2^{K39-81-85-111R}, or empty myc expression vector together with GFP-ELL1 or empty GFP expression vector for 36 h. The cell lysates were prepared for co-immunoprecipitation using anti-GFP antibody. The precipitates and whole cell lysates (1% input) were analyzed by immunoblotting using anti-myc and anti-GFP antibodies. GAPDH in the whole cell lysates was probed as loading control. (B) C4-2 cells were transfected with GFP, GFP-EAF2, GFP-EAF2^{K39-81-85-111R}, RFP, and RFP-ELL1 expression vector alone or in the indicated combinations for 48 h. Subcellular localization was imaged with confocal microscopy. Image enlargement: 100×. Data shown are representative of three independent experiments.