Cdk2-dependent and -independent pathways in E2F-mediated S phase induction

Yukinobu Arata, Masatoshi Fujita, Kiyoshi Ohtani, Sho Kijima, Jun Ya Kato

研究成果: ジャーナルへの寄稿学術誌査読

72 被引用数 (Scopus)

抄録

The transcription factor E2F plays an important role in G1 to S phase transition in the higher eukaryotic cell cycle. Although a number of E2F- inducible genes have been identified, the biochemical cascades from E2F to the S phase entry remain to be investigated. In this study, we generated stably transfected mouse NIH3T3 cells that express exogenous human E2F-1 under the control of a heavy metal-inducible metallothionein promoter and analyzed the molecular mechanism of the E2F-1-mediated initiation of chromosomal DNA replication. Ectopic E2F-1 expression in cells arrested in G0/G1 by serum deprivation enabled them to progress through G1 and to enter S phase. During the G1 progression, mouse cyclin E, but little of cyclin D1, was induced to express, which subsequently activated Cdk2. Experiments using the Cdk inhibitory proteins p27, p18, and p19 proved that the activity of Cdk2, but not of Cdk4, was required for S phase entry mediated by E2F-1. Minichromosome maintenance proteins (MCM) 4 and 7, the components of the DNA-replication initiation complex (RC), were constitutively expressed during the cell cycle, although the MCM genes are well known E2F-inducible genes. However, tight association of these two proteins with chromatin depended upon ectopic E2F-1 expression. In contrast, the Cdc45 protein, another RC component, which turned out to be a transcriptional target of E2Fs, was induced to express and subsequently bound to chromatin in response to E2F-1. Experiments utilizing a chemical Cdk- specific inhibitor, butyrolactone I, revealed that Cdk2 activity was required only for chromatin binding of the Cdc45 proteins, and not for the expression of Cdc45 or chromatin binding of MCM4 and -7. These results indicate that at least two separate pathways function downstream of E2F to initiate S phase; one depends upon the activity of Cdk2 and the other does not.

本文言語英語
ページ(範囲)6337-6345
ページ数9
ジャーナルJournal of Biological Chemistry
275
9
DOI
出版ステータス出版済み - 3月 3 2000
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 生化学
  • 分子生物学
  • 細胞生物学

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