首页 | 本学科首页   官方微博 | 高级检索  
     


CrxOS maintains the self-renewal capacity of murine embryonic stem cells
Authors:Ryota Saito  Tokiwa Yamasaki  Yoko Nagai  Jinzhan Wu  Hiroaki Kajiho  Eiichiro Noda  Sachiko Nishina  Noriyuki Azuma  Hiroshi Nishina
Affiliation:a Department of Developmental and Regenerative Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo 113-8510, Japan
b Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo 113-0033, Japan
c Department of Ophthalmology, National Center for Child Health and Development, Tokyo 157-8535, Japan
d Laboratory for Pluripotent Cell Studies, RIKEN Center for Developmental Biology, Hyogo 650-0047, Japan
Abstract:Embryonic stem (ES) cells maintain pluripotency by self-renewal. Several homeoproteins, including Oct3/4 and Nanog, are known to be key factors in maintaining the self-renewal capacity of ES cells. However, other genes required for the mechanisms underlying this process are still unclear. Here we report the identification by in silico analysis of a homeobox-containing gene, CrxOS, that is specifically expressed in murine ES cells and is essential for their self-renewal. ES cells mainly express the short isoform of endogenous CrxOS. Using a polyoma-based episomal expression system, we demonstrate that overexpression of the CrxOS short isoform is sufficient for maintaining the undifferentiated morphology of ES cells and stimulating their proliferation. Finally, using RNA interference, we show that CrxOS is essential for the self-renewal of ES cells, and provisionally identify foxD3 as a downstream target gene of CrxOS. To our knowledge, ours is the first delineation of the physiological role of CrxOS in ES cells.
Keywords:Embryonic stem cell   Self-renewal   In silico   Homeoprotein   CrxOS   foxD3
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号