Alternative Translation of OCT4 by an Internal Ribosome Entry Site and its Novel Function in Stress Response

Author:

Wang Xia12,Zhao Yannan1,Xiao Zhifeng1,Chen Bing1,Wei Zhanliang1,Wang Bin1,Zhang Jing1,Han Jin1,Gao Yuan1,Li Lingsong3,Zhao Hongxi3,Zhao Wenxue1,Lin Hang1,Dai Jianwu1

Affiliation:

1. Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China

2. The Graduate School, Chinese Academy of Sciences, Beijing, China

3. Stem Cell Research Center, Peking University, Beijing, China

Abstract

Abstract OCT4 is a pivotal transcription factor in maintaining the pluripotency and self-renewal capacities of embryonic stem (ES) cells. Human OCT4 can generate two isoforms by alternative splicing, termed OCT4A and OCT4B. OCT4A confers the stemness properties of ES cells, whereas the function of OCT4B is unknown. We present here the diverse protein products and a novel function of OCT4 gene. A single OCT4B mRNA can encode three isoforms by alternative translation initiation at AUG and CUG start codons, respectively. A putative internal ribosome entry site (IRES) has been identified in OCT4B mRNA accounting for the translation mechanism. The OCT4B-190 is upregulated under stress conditions and it may protect cell against apoptosis under stress. This work evokes the significance to distinguish the biological function of the protein products of OCT4. The OCT4 gene, by the regulation of alternative splicing and alternative translation initiation, may carry out more crucial roles in many biological events. Disclosure of potential conflicts of interest is found at the end of this article.

Funder

Ministry of Science and Technology of China

NSFC

Chinese Academy of Sciences

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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