Literature DB >> 10532314

The homeodomain transcription factor CDP/cut interacts with the cell cycle regulatory element of histone H4 genes packaged into nucleosomes.

T J Last1, A J van Wijnen, M C de Ridder, G S Stein, J L Stein.   

Abstract

The homeodomain transcription factor CDP/cut contains four separate DNA binding domains and interacts with large segments of DNA. Thus, CDP/cut has the potential to function as an architectural protein and perhaps to support modifications in chromatin structure and nucleosomal organization. To begin to examine the ability of CDP/cut to interact with chromatin, we analyzed binding of CDP/cut to the histone H4 gene promoter (-90 to +75) reconstituted into nucleosome cores. The -90 to +75 region encompasses the cell cycle regulatory element (Site II) that controls histone H4 gene transcription, a CDP/cut binding site and a nuclease hypersensitive region. Using electrophoretic mobility shift assays and DNase I footprinting experiments, we show that CDP/cut specifically interacts with its recognition motif in a nucleosomal context without displacing the nucleosome core. The competency of CDP/cut to interact with nucleosomes suggests that this transcription factor may facilitate chromatin remodeling in response to cell cycle regulatory and/or developmental cues.

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Year:  1999        PMID: 10532314     DOI: 10.1023/a:1007058123699

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  60 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-10       Impact factor: 11.205

Review 5.  Nucleosome positioning and modification: chromatin structures that potentiate transcription.

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Journal:  Trends Biochem Sci       Date:  1994-06       Impact factor: 13.807

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Journal:  Cell       Date:  1990-03-09       Impact factor: 41.582

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Journal:  J Biol Chem       Date:  1991-09-05       Impact factor: 5.157

8.  Hair defects and pup loss in mice with targeted deletion of the first cut repeat domain of the Cux/CDP homeoprotein gene.

Authors:  C Tufarelli; Y Fujiwara; D C Zappulla; E J Neufeld
Journal:  Dev Biol       Date:  1998-08-01       Impact factor: 3.582

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Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

10.  Stimulation of transcription factor binding and histone displacement by nucleosome assembly protein 1 and nucleoplasmin requires disruption of the histone octamer.

Authors:  P P Walter; T A Owen-Hughes; J Côté; J L Workman
Journal:  Mol Cell Biol       Date:  1995-11       Impact factor: 4.272

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  6 in total

1.  Impact of CUX2 on the female mouse liver transcriptome: activation of female-biased genes and repression of male-biased genes.

Authors:  Tara L Conforto; Yijing Zhang; Jennifer Sherman; David J Waxman
Journal:  Mol Cell Biol       Date:  2012-09-10       Impact factor: 4.272

2.  Regulation of the homeodomain CCAAT displacement/cut protein function by histone acetyltransferases p300/CREB-binding protein (CBP)-associated factor and CBP.

Authors:  S Li; B Aufiero; R L Schiltz; M J Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

3.  The p110 isoform of the CDP/Cux transcription factor accelerates entry into S phase.

Authors:  Laurent Sansregret; Brigitte Goulet; Ryoko Harada; Brian Wilson; Lam Leduy; Jacques Bertoglio; Alain Nepveu
Journal:  Mol Cell Biol       Date:  2006-03       Impact factor: 4.272

4.  Functional coupling of transcription factor HiNF-P and histone H4 gene expression during pre- and post-natal mouse development.

Authors:  Li-Jun Liu; Ronglin Xie; Sadiq Hussain; Jane B Lian; Jaime Rivera-Perez; Stephen N Jones; Janet L Stein; Gary S Stein; Andre J van Wijnen
Journal:  Gene       Date:  2011-05-13       Impact factor: 3.688

5.  CDP/Cux stimulates transcription from the DNA polymerase alpha gene promoter.

Authors:  Mary Truscott; Lélia Raynal; Peter Premdas; Brigitte Goulet; Lam Leduy; Ginette Bérubé; Alain Nepveu
Journal:  Mol Cell Biol       Date:  2003-04       Impact factor: 4.272

6.  CCAAT displacement protein/cut homolog recruits G9a histone lysine methyltransferase to repress transcription.

Authors:  Hitomi Nishio; Martin J Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-21       Impact factor: 11.205

  6 in total

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