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

Xia Wang(Chinese Academy of Sciences), Yannan Zhao(Chinese Academy of Sciences), Zhifeng Xiao(Chinese Academy of Sciences), Bing Chen(Chinese Academy of Sciences), Zhanliang Wei(Chinese Academy of Sciences), Bin Wang(Chinese Academy of Sciences), Jing Zhang(Chinese Academy of Sciences), Jin Han(Chinese Academy of Sciences), Yuan Gao(Chinese Academy of Sciences), Lingsong Li(Peking University), Hongxi Zhao(Peking University), Wenxue Zhao(Chinese Academy of Sciences), Hang Lin(Chinese Academy of Sciences), Jianwu Dai(Chinese Academy of Sciences)
Stem Cells
March 12, 2009
Cited by 111Open Access
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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.


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