Accession PRJCA014280
Title FACT Functions in Pluripotency State Transition of mESC
Relevance Model organism
Data types Raw sequence reads
ChIP-seq and RNA-seq
Organisms Mus musculus
Description mESCs with SSRP1-Q265K mutation showed increased spontaneous naive to formative phase transition, indicating the function of FACT in promoting cell fate decision. Surprisingly, the SSRP1-Q265K mutation increased formative gene expression and FACT binding at enhancers regulating formative genes, suggesting that FACT regulates transcription by regulating enhancers. Furthermore, this regulation potentially depends on eRNA transcription. In summary, this study proposes a novel mechanism that FACT controls formative gene expression through enhancers, which provides new insights into the functions of epigenetic regulation in pluripotency control during embryonic development.
Sample scope Multiisolate
Release date 2024-01-22
Grants
Agency program Grant ID Grant title
National Natural Science Foundation of China (NSFC) 31725015
National Natural Science Foundation of China (NSFC) 31830048
National Natural Science Foundation of China (NSFC) 31861143041
National Natural Science Foundation of China (NSFC) 31671332
Beijing Outstanding Young Scientist Program BJJWZYJH01201910001005
National Key Research and Development Project of China 2019YFA0508903
Funding for open access charge: Beijing Outstanding Young Scientist Program BJJWZYJH01201910001005
National Natural Science Foundation of China, Youth Program 31900433
Submitter Qing    Li  (li.qing@pku.edu.cn)
Organization Peking University
Submission date 2023-01-06

Project Data

Resource name Description
BioSample (4) -
SAMC3130136 Q265K_SL2i_SSRP1_ChIP_rep2
SAMC3130135 Q265K_SL2i_SSRP1_ChIP_rep1
SAMC3130134 WT_SL2i_SSRP1_ChIP_rep2
SAMC3130133 WT_SL2i_SSRP1_ChIP_rep1
GSA (1) -
CRA013178 Pluripotency state transition of embryonic stem cells requires the turnover of histone chaperone FACT on chromatin