Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/105783
Title: p27Kip1 and p21Cip1 collaborate in the regulation of transcription by recruiting cyclin-Cdk complexes on the promoters of target genes
Author: Orlando, Serena
Gallastegui Calvache, Edurne, 1982-
Besson, Arnaud
Abril, Gabriel
Aligué i Alemany, Rosa Maria
Pujol Sobrevía, María Jesús
Bachs Valldeneu, Oriol
Keywords: Expressió gènica
Inhibidors enzimàtics
Proteïnes quinases
Gene expression
Enzyme inhibitors
Protein kinases
Issue Date: 18-Aug-2015
Publisher: Oxford University Press
Abstract: Transcriptional repressor complexes containing p130 and E2F4 regulate the expression of genes involved in DNA replication. During the G1 phase of the cell cycle, sequential phosphorylation of p130 by cyclin-dependent kinases (Cdks) disrupts these complexes allowing gene expression. The Cdk inhibitor and tumor suppressor p27(Kip1) associates with p130 and E2F4 by its carboxyl domain on the promoters of target genes but its role in the regulation of transcription remains unclear. We report here that p27(Kip1) recruits cyclin D2/D3-Cdk4 complexes on the promoters by its amino terminal domain in early and mid G1. In cells lacking p27(Kip1), cyclin D2/D3-Cdk4 did not associate to the promoters and phosphorylation of p130 and transcription of target genes was increased. In late G1, these complexes were substituted by p21(Cip1)-cyclin D1-Cdk2. In p21(Cip1) null cells cyclin D1-Cdk2 were not found on the promoters and transcription was elevated. In p21/p27 double null cells transcription was higher than in control cells and single knock out cells. Thus, our results clarify the role of p27(Kip1) and p21(Cip1) in transcriptional regulation of genes repressed by p130/E2F4 complexes in which p27(Kip1) and p21(Cip1) play a sequential role by recruiting and regulating the activity of specific cyclin-Cdk complexes on the promoters
Note: Reproducció del document publicat a: https://doi.org/10.1093/nar/gkv593
It is part of: Nucleic Acids Research, 2015, vol. 43 , num. 14, p. 6860-6873
Related resource: https://doi.org/10.1093/nar/gkv593
URI: http://hdl.handle.net/2445/105783
ISSN: 0305-1048
Appears in Collections:Articles publicats en revistes (Biomedicina)

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