1999
DOI: 10.2741/a466
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Transcription factors in DNA replication

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Cited by 17 publications
(7 citation statements)
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“…JUND is the most broadly expressed member of the JUN family of transcription factors and in its absence primary murine fibroblasts undergo a p53‐dependent cell cycle arrest and premature senescence. The exact mechanism by which these transcription factors enhance DNA replication remains unknown, but may include recruitment of the DNA replication machinery through protein–protein interactions, modulation of chromatin structure, mediation of nuclear matrix attachment of the origins, or by regulating transcription, thereby affecting DNA replication (reviewed in [Murakami and Ito, 1999).…”
Section: Discussionmentioning
confidence: 99%
“…JUND is the most broadly expressed member of the JUN family of transcription factors and in its absence primary murine fibroblasts undergo a p53‐dependent cell cycle arrest and premature senescence. The exact mechanism by which these transcription factors enhance DNA replication remains unknown, but may include recruitment of the DNA replication machinery through protein–protein interactions, modulation of chromatin structure, mediation of nuclear matrix attachment of the origins, or by regulating transcription, thereby affecting DNA replication (reviewed in [Murakami and Ito, 1999).…”
Section: Discussionmentioning
confidence: 99%
“…In mammals, many transcription factors are proto-oncogenes, including c-Jun, c-Myb, and c-Myc (20,73). Their oncogenicity is thought to be due to dysregulation of the transcription that they promote.…”
Section: Ecdyson Signals Could Regulate Chorion Gene Amplification In Drosophila Developmentmentioning
confidence: 99%
“…Indeed, some of these transcription factors may also play a direct role in initiating replication; for example, some replication origins in higher eukaryotes are located in promoter regions of genes such as c-myc, and replication near the c-myc promoter can indeed be induced in a model replication system ͑specifically, the negative supercoiling introduced by transcription induced the unwinding of the DNA duplex at the origin sequence͒. 15 Another intriguing observation is that the CDKactivating kinase, CAK, has been found to be a component of protein complexes involved in the basal transcription machinery and that CAK can phosphorylate RNA polymerase II; 16 thus, CAK can also provide a direct link between cell cycle control and transcription.…”
Section: B Transcriptional Regulation Of S-phase Entrymentioning
confidence: 99%