Che-1 affects cell growth by interfering with the recruitment of HDAC1 by Rb (Q28216052)

6

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Tiziana Bruno

1

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Monica Di Padova

5

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Francesca De Nicola

3

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author name string

Roberta De Angelis

2

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Christian Barbato

4

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Valentina Libri

7

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Barbara Benassi

8

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Elisabetta Mattei

9

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Alberto Chersi

10

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Aristide Floridi

12

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Claudio Passananti

13

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Maurizio Fanciulli

Reconstitution of hTERT restores tumorigenicity in melanoma-derived c-Myc low-expressing clones

14

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language of work or name

English

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publication date

November 2002

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published in

Cancer Cell

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volume

2

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issue

5

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page(s)

387-99

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cites work

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Identification of a novel partner of RNA polymerase II subunit 11, Che-1, which interacts with and affects the growth suppression function of Rb

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The three members of the pocket proteins family share the ability to repress E2F activity through recruitment of a histone deacetylase

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Cell cycle-dependent recruitment of HDAC-1 correlates with deacetylation of histone H4 on an Rb-E2F target promoter

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Tight control of gene expression in mammalian cells by tetracycline-responsive promoters

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The retinoblastoma protein binds E2F residues required for activation in vivo and TBP binding in vitro

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The Rb/E2F pathway: expanding roles and emerging paradigms

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Cdk phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1

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Histone deacetylase activity is required for full transcriptional repression by mSin3A

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A signature motif in transcriptional co-activators mediates binding to nuclear receptors

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ATP-dependent remodeling and acetylation as regulators of chromatin fluidity

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C-terminal truncation of Dlk/ZIP kinase leads to abrogation of nuclear transport and high apoptotic activity

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Twenty-five years of the nucleosome, fundamental particle of the eukaryote chromosome

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E2F1 overexpression in quiescent fibroblasts leads to induction of cellular DNA synthesis and apoptosis.

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RBP1 recruits both histone deacetylase-dependent and -independent repression activities to retinoblastoma family proteins

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Rb interacts with histone deacetylase to repress transcription

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Retinoblastoma protein represses transcription by recruiting a histone deacetylase

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Role of the Rb/E2F pathway in cell growth control

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The retinoblastoma protein: more than a tumor suppressor

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The transcriptional co-activator p/CIP binds CBP and mediates nuclear-receptor function

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Association between an oncogene and an anti-oncogene: the adenovirus E1A proteins bind to the retinoblastoma gene product

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Chromatin disruption and modification

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Exit from G1 and S phase of the cell cycle is regulated by repressor complexes containing HDAC-Rb-hSWI/SNF and Rb-hSWI/SNF

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