Wdr5 Mediates Self-Renewal and Reprogramming via the Embryonic Stem Cell Core Transcriptional Network

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• 作者：Yen-Sin Ang¹ ; ² ; ³ ; ^{yen-sin.ang@mssm.edu} ; Su-Yi Tsai¹ ; ³ ; ⁵ ; Dung-Fang Lee¹ ; ² ; ³ ; ⁷ ; Jonathan Monk¹ ; ² ; ⁷ ; Jie Su¹ ; ² ; ³ ; ⁷ ; Kajan Ratnakumar¹ ; ⁴ ; ⁵ ; Junjun Ding¹ ; ³ ; Yongchao Ge⁶ ; Henia Darr¹ ; ² ; ³ ; Betty Chang¹ ; ² ; ³ ; Jianlong Wang¹ ; ³ ; Michael Rendl¹ ; ³ ; ⁵ ; Emily Bernstein¹ ; ⁴ ; ⁵ ; ⁷ ; Christoph Schaniel¹ ; ² ; ⁷ ; Ihor  ; R. Lemischka¹ ; ² ; ³ ; ^{ihor.lemischka@mssm.edu}
• 刊名：Cell
• 出版年：2011
• 出版时间：15 April 2011
• 年：2011
• 卷：145
• 期：2
• 页码：183-197
• 全文大小：2246 K

文摘

Summary

The embryonic stem (ES) cell transcriptional and chromatin-modifying networks are critical for self-renewal maintenance. However, it remains unclear whether these networks functionally interact and, if so, what factors mediate such interactions. Here, we show that WD repeat domain 5 (Wdr5), a core member of the mammalian Trithorax (trxG) complex, positively correlates with the undifferentiated state and is a regulator of ES cell self-renewal. We demonstrate that Wdr5, an “effector” of H3K4 methylation, interacts with the pluripotency transcription factor Oct4. Genome-wide protein localization and transcriptome analyses demonstrate overlapping gene regulatory functions between Oct4 and Wdr5. The Oct4-Sox2-Nanog circuitry and trxG cooperate in activating transcription of key self-renewal regulators, and furthermore, Wdr5 expression is required for the efficient formation of induced pluripotent stem (iPS) cells. We propose an integrated model of transcriptional and epigenetic control, mediated by select trxG members, for the maintenance of ES cell self-renewal and somatic cell reprogramming.