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Inability to enter S phase and defective RNA polymerase II CTD phosphorylation in mice lacking Mat1
Author(s) -
Rossi Derrick J.,
Londesborough Anou,
Korsisaari Nina,
Pihlak Arno,
Lehtonen Eero,
Henkemeyer Mark,
Mäkelä Tomi P.
Publication year - 2001
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/20.11.2844
Subject(s) - library science , biology , rna polymerase ii , genetics , computer science , gene , gene expression , promoter
The trimeric Cdk7–cyclin H–Mat1 complex comprises the kinase subunit of basal transcription factor TFIIH and has been shown to function as a cyclin‐dependent kinase (Cdk)‐activating kinase. Herein we report that disruption of the murine Mat1 gene leads to peri‐implantation lethality coincident with depletion of maternal Mat1 protein. In culture, Mat1 −/− blastocysts gave rise to viable post‐mitotic trophoblast giant cells while mitotic lineages failed to proliferate and survive. In contrast to wild‐type trophoblast giant cells, Mat1 −/− cells exhibited a rapid arrest in endoreduplication, which was characterized by an inability to enter S phase. Additionally, Mat1 −/− cells exhibited defects in phosphorylation of the C‐terminal domain (CTD) of RNA polymerase II on both Ser5 and Ser2 of the heptapeptide repeat. Despite this, Mat1 −/− cells demonstrated apparent transcriptional and translational integrity. These data indicate an essential role for Mat1 in progression through the endocycle and suggest that while Mat1 modulates CTD phosphorylation, it does not appear to be essential for RNA polymerase II‐mediated transcription.