The role of Zfp352 in the regulation of transient expression of 2‐cell specific genes in mouse embryonic stem cells

Author:

Mwalilino Lusubilo1,Yamane Mariko123,Ishiguro Kei‐ichiro4ORCID,Usuki Shingo5,Endoh Mitsuhiro1,Niwa Hitoshi1ORCID

Affiliation:

1. Department of Pluripotent Stem Cell Biology, Institute of Molecular Embryology and Genetics Kumamoto University Kumamoto Japan

2. Department of Functional Genome Informatics, Division of Medical Genomics, Medical Research Institute Tokyo Medical and Dental University Tokyo Japan

3. Laboratory for Bioinformatics Research RIKEN Center for Biosystems Dynamics Research Kobe Japan

4. Department of Chromosome Biology, Institute of Molecular Embryology and Genetics Kumamoto University Kumamoto Japan

5. Liaison Laboratory Research Promotion Center, IMEG Kumamoto University Kumamoto Japan

Abstract

AbstractMouse ES cell populations contain a minor sub‐population that expresses genes specifically expressed in 2‐cell stage embryos. This sub‐population consists of 2‐cell‐gene labeled cells (2CLCs) generated by the transient activation of the 2‐cell specific genes initiated by the master regulator, Dux. However, the mechanism regulating the transient expression remains largely unclear. Here we reported a novel function of Zfp352, one of the 2‐cell specific genes, in regulating the 2CLC sub‐population. Zfp352 encodes zinc‐finger transcription factor belonging to the Klf family. Dux transiently activates Zfp352 after the activation of Zscan4c in a subset of the 2CLC subpopulation. Interestingly, in the reporter assay, the transcriptional activation of Zscan4c by Dux is strongly repressed by the co‐expression of Zfp352. However, the knockout of Zfp352 resulted in the repression of a subset of the 2‐cell‐specific genes. These data suggest the dual roles of Zfp352 in regulating the transient activation of the 2‐cell‐specific genes.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Cell Biology,Genetics

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