A role for NANOG in G1 to S transition in human embryonic stem cells through direct binding of CDK6 and CDC25A

Author:

Zhang Xin12,Neganova Irina12,Przyborski Stefan13,Yang Chunbo12,Cooke Michael13,Atkinson Stuart P.12,Anyfantis George12,Fenyk Stefan13,Keith W. Nicol4,Hoare Stacey F.4,Hughes Owen12,Strachan Tom12,Stojkovic Miodrag1,Hinds Philip W.5,Armstrong Lyle12,Lako Majlinda12

Affiliation:

1. NorthEast England Stem Cell Institute

2. Institute of Human Genetics, Newcastle University, International Centre for Life, Newcastle upon Tyne NE1 3BZ, England, UK

3. School of Biological and Biomedical Sciences, Durham University, Durham DH1 3LE, England, UK

4. Centre for Oncology and Applied Pharmacology, University of Glasgow, Cancer Research UK Beatson Laboratories, Glasgow G61 1BD, Scotland, UK

5. Molecular Oncology Research Institute, Tufts Medical Center, Tufts University, Boston, MA 02111

Abstract

In this study, we show that NANOG, a master transcription factor, regulates S-phase entry in human embryonic stem cells (hESCs) via transcriptional regulation of cell cycle regulatory components. Chromatin immunoprecipitation combined with reporter-based transfection assays show that the C-terminal region of NANOG binds to the regulatory regions of CDK6 and CDC25A genes under normal physiological conditions. Decreased CDK6 and CDC25A expression in hESCs suggest that both CDK6 and CDC25A are involved in S-phase regulation. The effects of NANOG overexpression on S-phase regulation are mitigated by the down-regulation of CDK6 or CDC25A alone. Overexpression of CDK6 or CDC25A alone can rescue the impact of NANOG down-regulation on S-phase entry, suggesting that CDK6 and CDC25A are downstream cell cycle effectors of NANOG during the G1 to S transition.

Publisher

Rockefeller University Press

Subject

Cell Biology

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