Back to Search
Start Over
Max is a repressor of germ cell-related gene expression in mouse embryonic stem cells.
- Source :
-
Nature communications [Nat Commun] 2013; Vol. 4, pp. 1754. - Publication Year :
- 2013
-
Abstract
- Embryonic stem cells and primordial germ cells (PGCs) express many pluripotency-associated genes, but embryonic stem cells do not normally undergo conversion into primordial germ cells. Thus, we predicted that there is a mechanism that represses primordial germ cell-related gene expression in embryonic stem cells. Here we identify genes involved in this putative mechanism, by using an embryonic stem cell line with a Vasa reporter in an RNA interference screen of transcription factor genes expressed in embryonic stem cells. We identify five genes that result in the expression of Vasa when silenced. Of these, Max is the most striking. Transcriptome analysis reveals that Max knockdown in embryonic stem cells results in selective, global derepression of germ cell-specific genes. Max interacts with histone H3K9 methyltransferases and associates with the germ cell-specific genes in embryonic stem cells. In addition, Max knockdown results in a decrease in histone H3K9 dimethylation at their promoter regions. We propose that Max is part of protein complex that acts as a repressor of germ cell-related genes in embryonic stem cells.
- Subjects :
- Animals
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors genetics
Biomarkers metabolism
Cell Line
DEAD-box RNA Helicases genetics
Embryonic Stem Cells cytology
Flow Cytometry
Gene Knockdown Techniques
Genes, Reporter
Germ Cells cytology
Histone Methyltransferases
Histone-Lysine N-Methyltransferase metabolism
Histones metabolism
Lysine metabolism
Meiosis genetics
Methylation
Mice
Mice, Inbred C57BL
Oligonucleotide Array Sequence Analysis
Promoter Regions, Genetic genetics
Protein Binding
RNA Interference
Repressor Proteins
Spermatogenesis genetics
Time Factors
Up-Regulation genetics
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors metabolism
Embryonic Stem Cells metabolism
Gene Expression Regulation, Developmental
Germ Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 4
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 23612295
- Full Text :
- https://doi.org/10.1038/ncomms2780