Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases. (Q39540142)

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scientific article published on November 2000

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English	Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases.	scientific article published on November 2000

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1 November 2019

Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases (English)

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1 November 2019

Mark Featherstone

4

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1 November 2019

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M Saleh

1

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1 November 2019

I Rambaldi

2

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1 November 2019

X J Yang

3

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1 November 2019

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1 November 2000

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1 November 2019

Molecular and Cellular Biology

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1 November 2019

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1 November 2019

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1 November 2019

8623-8633

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1 November 2019

A conformational change in PBX1A is necessary for its nuclear localization

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Acetylation of histones and transcription-related factors

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A core SMRT corepressor complex containing HDAC3 and TBL1, a WD40-repeat protein linked to deafness

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Roles of Hoxa1 and Hoxa2 in patterning the early hindbrain of the mouse

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Sin meets NuRD and other tails of repression.

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Pbx-Hox heterodimers recruit coactivator-corepressor complexes in an isoform-specific manner

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HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor

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PBX and MEIS as non-DNA-binding partners in trimeric complexes with HOX proteins

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CBP and histone deacetylase inhibition enhance the transactivation potential of the HOXB7 homeodomain-containing protein

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Activity regulation of Hox proteins, a mechanism for altering functional specificity in development and evolution

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HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells

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Histone acetylases and deacetylases in cell proliferation

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Activity regulation of a Hox protein and a role for the homeodomain in inhibiting transcriptional activation

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A genetic screen of the Drosophila X chromosome for mutations that modify Deformed function.

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Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300

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Histone acetylation and transcriptional regulatory mechanisms

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The novel homeoprotein Prep1 modulates Pbx-Hox protein cooperativity

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Prep1, a novel functional partner of Pbx proteins.

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13 September 2017

Genetic interactions between Hoxa1 and Hoxb1 reveal new roles in regulation of early hindbrain patterning

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Meis1 and pKnox1 bind DNA cooperatively with Pbx1 utilizing an interaction surface disrupted in oncoprotein E2a-Pbx1

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Isolation and characterization of cDNAs corresponding to an additional member of the human histone deacetylase gene family

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Meis proteins are major in vivo DNA binding partners for wild-type but not chimeric Pbx proteins

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The multifunctional role of the co-activator CBP in transcriptional regulation

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Pbx raises the DNA binding specificity but not the selectivity of antennapedia Hox proteins

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Nuclear receptor repression mediated by a complex containing SMRT, mSin3A, and histone deacetylase

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Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3

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13 September 2017

Distinct HOX N-terminal arm residues are responsible for specificity of DNA recognition by HOX monomers and HOX.PBX heterodimers

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13 September 2017

The Abd-B-like Hox homeodomain proteins can be subdivided by the ability to form complexes with Pbx1a on a novel DNA target

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Transcriptional repression by YY1 is mediated by interaction with a mammalian homolog of the yeast global regulator RPD3

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Cloning and expression of a new HOXC6 transcript encoding a repressing protein

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13 September 2017

The human cut homeodomain protein can repress gene expression by two distinct mechanisms: active repression and competition for binding site occupancy

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Role of CBP/P300 in nuclear receptor signalling

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A p300/CBP-associated factor that competes with the adenoviral oncoprotein E1A

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In vitro and transgenic analysis of a human HOXD4 retinoid-responsive enhancer

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Repression by HoxA7 is mediated by the homeodomain and the modulatory action of its N-terminal-arm residues

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A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors

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Selective repression of transcriptional activators by Pbx1 does not require the homeodomain

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Mapping and mutagenesis of the amino-terminal transcriptional repression domain of the Drosophila Krüppel protein

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Identification of a retinoic acid response element upstream of the murine Hox-4.2 gene

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Hox genes in vertebrate development

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A proline-rich transcriptional activation domain in murine HOXD-4 (HOX-4.2).

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Pbx proteins display hexapeptide-dependent cooperative DNA binding with a subset of Hox proteins

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Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

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Cooperative interactions between HOX and PBX proteins mediated by a conserved peptide motif

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Oncogenic conversion of transcription factors by chromosomal translocations

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Homeodomain-DNA recognition

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21 August 2018

Functional dominance among Hox genes: repression dominates activation in the regulation of Dpp.

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21 August 2018

Expression of the murine Hoxa4 gene requires both autoregulation and a conserved retinoic acid response element

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21 August 2018

The Pbx family of proteins is strongly upregulated by a post-transcriptional mechanism during retinoic acid-induced differentiation of P19 embryonal carcinoma cells.

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Drosophila Hox complex downstream targets and the function of homeotic genes

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Antagonizing cAMP-dependent protein kinase A in the dorsal CNS activates a conserved Sonic hedgehog signaling pathway.

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cAMP, an activator of protein kinase A, suppresses the expression of sonic hedgehog

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102167

21 August 2018

Role of a conserved retinoic acid response element in rhombomere restriction of Hoxb-1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102167

21 August 2018

A conserved retinoic acid response element required for early expression of the homeobox gene Hoxb-1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102167

21 August 2018

Segmental expression of Hoxb-1 is controlled by a highly conserved autoregulatory loop dependent upon exd/pbx

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102167

21 August 2018

Ectopic Hoxa-1 induces rhombomere transformation in mouse hindbrain

1 reference

https://pubmed.ncbi.nlm.nih.gov/11046157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell-cell interaction modulates myoD-induced skeletal myogenesis of pluripotent P19 cells in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/11046157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Residues flanking the HOX YPWM motif contribute to cooperative interactions with PBX

1 reference

https://pubmed.ncbi.nlm.nih.gov/11046157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hox proteins meet more partners

1 reference

https://pubmed.ncbi.nlm.nih.gov/11046157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for RNA processing in regulating expression from transfected genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/11046157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Murine hoxd4 expression in the CNS requires multiple elements including a retinoic acid response element

1 reference

https://pubmed.ncbi.nlm.nih.gov/11046157

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.20.22.8623-8633.2000

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11046157%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11046157%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11046157%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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