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Smad6 as a transcriptional corepressor

  • University of Alabama at Birmingham
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Smad6 and Smad7, a subgroup of Smad proteins, antagonize the signals elicited by transforming growth factor-β. These two Smads, induced by transforming growth factor-β or bone morphogenetic protein (BMP) stimulation, form stable associations with their activated type I receptors, blocking phosphorylation of receptor-regulated Smads in the cytoplasm. Here we show that Smad6 interacts with homeobox (Hox) c-8 as a transcriptional corepressor, inhibiting BMP signaling in the nucleus. The interaction between Smad6 and Hoxc-8 was identified by a yeast two-hybrid approach and further demonstrated by co-immunoprecipitation assays in cells. Gel shift assays show that Smad6, but not Smad7, interacts with both Hoxc-8 and Hoxa-9 as a heterodimer when binding to DNA. More importantly, the Smad6-Hoxc-8 complex inhibits interaction of Smad1 with Hoxc-8- and Smad1-induced transcription activity. These data indicate that Smad6 interacts with Hox transcription factors as part of the negative feedback circuit in the BMP signaling pathway.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 8267-8270 (4 pages)

Journal (Volume, Issue Number)

Journal of Biological Chemistry (Volume 275, Issue 12)

Publication milestones

  • Published - 03/24/2000

Publication status

Published - 03/24/2000

ISSN

0021-9258

Publication IDs

  • Scopus: 0034708801
  • PubMed: 10722652

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
2.81
SciVal
Author count
4
SciVal
citations
119
SciVal
Paper percentile
94
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1

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Mentions
4
Citation count
118
Captures
56

Funding Details

FunderFunding number
NIDDK
R01DK053757