TY - JOUR
T1 - Otx2 and Oct4 Drive Early Enhancer Activation during Embryonic Stem Cell Transition from Naive Pluripotency
AU - Yang, Shen Hsi
AU - Kalkan, Tüzer
AU - Morissroe, Claire
AU - Marks, Hendrik
AU - Stunnenberg, Hendrik
AU - Smith, Austin
AU - Sharrocks, Andrew D.
N1 - Funding Information:
We thank Karren Palmer for excellent technical assistance; Andy Hayes and Ian Donaldson in the Genomic Technologies and Bioinformatics facilities; Namshik Han and Aaron Webber for advice; and Nicoletta Bobola, Hilary Ashe, Xi Chen, and members of our laboratories for comments on the manuscript and stimulating discussions. This work was funded by the Wellcome Trust. A.S. is a Medical Research Council Professor.
PY - 2014/6/26
Y1 - 2014/6/26
N2 - Embryonic stem cells (ESCs) are unique in that they have the capacity to differentiate into all of the cell types in the body. We know a lot about the complex transcriptional control circuits that maintain the naive pluripotent state under self-renewing conditions but comparatively less about how cells exit from this state in response to differentiation stimuli. Here, we examined the role of Otx2 in this process in mouse ESCs and demonstrate that it plays a leading role in remodeling the gene regulatory networks as cells exit from ground state pluripotency. Otx2 drives enhancer activation through affecting chromatin marks and the activity of associated genes. Mechanistically, Oct4 is required for Otx2 expression, andreciprocally, Otx2 is required for efficient Oct4 recruitment to many enhancer regions. Therefore, the Oct4-Otx2 regulatory axis actively establishes anew regulatory chromatin landscape during the early events that accompany exit from ground state pluripotency.
AB - Embryonic stem cells (ESCs) are unique in that they have the capacity to differentiate into all of the cell types in the body. We know a lot about the complex transcriptional control circuits that maintain the naive pluripotent state under self-renewing conditions but comparatively less about how cells exit from this state in response to differentiation stimuli. Here, we examined the role of Otx2 in this process in mouse ESCs and demonstrate that it plays a leading role in remodeling the gene regulatory networks as cells exit from ground state pluripotency. Otx2 drives enhancer activation through affecting chromatin marks and the activity of associated genes. Mechanistically, Oct4 is required for Otx2 expression, andreciprocally, Otx2 is required for efficient Oct4 recruitment to many enhancer regions. Therefore, the Oct4-Otx2 regulatory axis actively establishes anew regulatory chromatin landscape during the early events that accompany exit from ground state pluripotency.
UR - http://www.scopus.com/inward/record.url?scp=84903473477&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2014.05.037
DO - 10.1016/j.celrep.2014.05.037
M3 - Article
C2 - 24931607
AN - SCOPUS:84903473477
SN - 2211-1247
VL - 7
SP - 1968
EP - 1981
JO - Cell Reports
JF - Cell Reports
IS - 6
ER -