RRC ID 59570
著者 Ou HL, Kim CS, Uszkoreit S, Wickström SA, Schumacher B.
タイトル Somatic Niche Cells Regulate the CEP-1/p53-Mediated DNA Damage Response in Primordial Germ Cells.
ジャーナル Dev Cell
Abstract Genome integrity in primordial germ cells (PGCs) is a prerequisite for fertility and species maintenance. In C. elegans, PGCs require global-genome nucleotide excision repair (GG-NER) to remove UV-induced DNA lesions. Failure to remove the lesions leads to the activation of the C. elegans p53, CEP-1, resulting in mitotic arrest of the PGCs. We show that the eIF4E2 translation initiation factor IFE-4 in somatic gonad precursor (SGP) niche cells regulates the CEP-1/p53-mediated DNA damage response (DDR) in PGCs. We determine that the IFE-4 translation target EGL-15/FGFR regulates the non-cell-autonomous DDR that is mediated via FGF-like signaling. Using hair follicle stem cells as a paradigm, we demonstrate that the eIF4E2-mediated niche cell regulation of the p53 response in stem cells is highly conserved in mammals. We thus reveal that the somatic niche regulates the CEP-1/p53-mediated DNA damage checkpoint in PGCs. Our data suggest that the somatic niche impacts the stability of heritable genomes.
巻・号 50(2)
ページ 167-183.e8
公開日 2019-7-22
DOI 10.1016/j.devcel.2019.06.012
PII S1534-5807(19)30530-1
PMID 31336098
MeSH Animals Apoptosis Caenorhabditis elegans Caenorhabditis elegans Proteins / genetics Caenorhabditis elegans Proteins / metabolism* Cells, Cultured DNA Damage* DNA Repair Eukaryotic Initiation Factors / genetics Eukaryotic Initiation Factors / metabolism* Female Fibroblast Growth Factors / metabolism* Germ Cells / metabolism Germ Cells / pathology* Male Mice Mice, Inbred C57BL Signal Transduction Tumor Suppressor Protein p53 / genetics Tumor Suppressor Protein p53 / metabolism*
IF 9.19
引用数 1
リソース情報
線虫 tm684 tm3886