Actl6a Protects Embryonic Stem Cells From Differentiating Into Primitive Endoderm. (21st May 2015)

• Record Type: Journal Article
• Authors: Lu, Weisi; Fang, Lekun; Ouyang, Bin; Zhang, Xiya; Zhan, Shaoquan; Feng, Xuyang; Bai, Yaofu; Han, Xin; Kim, Hyeung; He, Quanyuan; Wan, Ma; Shi, Feng‐Tao; Feng, Xin‐Hua; Liu, Dan; Huang, Junjiu; Songyang, Zhou
• Is Part Of: Stem cells. Volume 33:Number 6(2015:Jun.)
• Page Start: 1782
• Page End: 1793
• Publication Date: 2015-05-21
• Subjects: Actl6a -- Embryonic stem cells -- Self‐renewal -- Primitive endoderm -- Tip60‐p400 complex; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.2000
• Languages: English
• ISSNs: 1066-5099

Abstract

Abstract: Actl6a (actin‐like protein 6A, also known as Baf53a or Arp4) is a subunit shared by multiple complexes including esBAF, INO80, and Tip60‐p400, whose main components (Brg1, Ino80, and p400, respectively) are crucial for the maintenance of embryonic stem cells (ESCs). However, whether and how Actl6a functions in ESCs has not been investigated. ESCs originate from the epiblast (EPI) that is derived from the inner cell mass (ICM) in blastocysts, which also give rise to primitive endoderm (PrE). The molecular mechanisms for EPI/PrE specification remain unclear. In this study, we provide the first evidence that Actl6a can protect mouse ESCs (mESCs) from differentiating into PrE. While RNAi knockdown of Actl6a, which appeared highly expressed in mESCs and downregulated during differentiation, induced mESCs to differentiate towards the PrE lineage, ectopic expression of Actl6a was able to repress PrE differentiation. Our work also revealed that Actl6a could interact with Nanog and Sox2 and promote Nanog binding to pluripotency genes such as Oct4 and Sox2 . Interestingly, cells depleted of p400, but not of Brg1 or Ino80, displayed similar PrE differentiation patterns. Mutant Actl6a with impaired ability to bind Tip60 and p400 failed to block PrE differentiation induced by Actl6a dysfunction. Finally, we showed that Actl6a could target to the promoters of key PrE regulators (e.g., Sall4 and Fgf4), repressing their expression and inhibiting PrE differentiation. Our findings uncover a novel function of Actl6a in mESCs, where it acts as a gatekeeper to prevent mESCs from entering into the PrE lineage through a Yin/Yang regulating pattern. Stem Cells 2015;33:1782–1793