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The C. elegans Tousled-like kinase (TLK-1) has an essential role in transcription.
Han, Zhenbo; Saam, Jennifer R; Adams, Henry P; Mango, Susan E; Schumacher, Jill M.
Afiliação
  • Han Z; Department of Molecular Genetics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Curr Biol ; 13(22): 1921-9, 2003 Nov 11.
Article em En | MEDLINE | ID: mdl-14614817
ABSTRACT

BACKGROUND:

The Tousled kinases comprise an evolutionarily conserved family of proteins that have been previously implicated in chromatin remodeling, DNA replication, and DNA repair. Here, we used RNA mediated interference (RNAi) to determine the function of the C. elegans Tousled kinase (TLK-1) during embryonic development.

RESULTS:

TLK-1-deficient embryos arrested with a phenotype reminiscent of embryos that are broadly defective in transcription, and the expression of several reporter genes was dramatically reduced in tlk-1(RNAi) embryos. Furthermore, posttranslational modifications of RNA polymerase II (RNAPII) and histone H3 that have been correlated with transcription elongation, phosphorylation of the RNAPII CTD at Serine 2, and methylation of histone H3 at Lysine 36 were found at significantly reduced levels in tlk-1(RNAi) embryos as compared to wild-type.

CONCLUSIONS:

These results reveal a surprising requirement for a Tousled-like kinase in transcriptional regulation during development, likely during the elongation phase. In addition, our results confirm that the link between RNAPII phosphorylation and histone H3 methylation previously observed in budding yeast is functionally conserved in metazoans.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfotransferases / Transcrição Gênica / RNA Polimerase II / Proteínas Serina-Treonina Quinases / Caenorhabditis elegans / Metiltransferases Limite: Animals Idioma: En Revista: Curr Biol Ano de publicação: 2003 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfotransferases / Transcrição Gênica / RNA Polimerase II / Proteínas Serina-Treonina Quinases / Caenorhabditis elegans / Metiltransferases Limite: Animals Idioma: En Revista: Curr Biol Ano de publicação: 2003 Tipo de documento: Article