Literature DB >> 8878477

A transcriptional partner for MAD proteins in TGF-beta signalling.

X Chen1, M J Rubock, M Whitman.   

Abstract

The transforming-growth-factor-beta (TGF-beta) superfamily is critical for establishing mesoderm during early embryogenesis in Xenopus. The transcriptional activation of Mix.2, an immediate-early response gene specific to activin-like members of the TGF-beta superfamily, is associated with the rapid appearance of a site-specific DNA-binding activity that recognizes a fifty-base-pair regulatory element known as ARE in the Mix.2 promoter. Cloning of the site-specific DNA-binding component of this activity revealed it to be a new winged-helix transcription factor and a direct target for signalling by the TGF-beta superfamily. XMAD2, a recently identified TGF-beta signal transducer, forms a complex with the transcription factor in an activin-dependent fashion to generate an activated ARE-binding complex. A model is proposed to explain how TGF-beta superfamily signals might regulate the expression of specific genes in the early embryo.

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Year:  1996        PMID: 8878477     DOI: 10.1038/383691a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  153 in total

1.  Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif.

Authors:  S Germain; M Howell; G M Esslemont; C S Hill
Journal:  Genes Dev       Date:  2000-02-15       Impact factor: 11.361

Review 2.  Transcriptional control by the TGF-beta/Smad signaling system.

Authors:  J Massagué; D Wotton
Journal:  EMBO J       Date:  2000-04-17       Impact factor: 11.598

3.  The winged-helix/forkhead protein myocyte nuclear factor beta (MNF-beta) forms a co-repressor complex with mammalian sin3B.

Authors:  Q Yang; Y Kong; B Rothermel; D J Garry; R Bassel-Duby; R S Williams
Journal:  Biochem J       Date:  2000-01-15       Impact factor: 3.857

4.  A mechanism of repression of TGFbeta/ Smad signaling by oncogenic Ras.

Authors:  M Kretzschmar; J Doody; I Timokhina; J Massagué
Journal:  Genes Dev       Date:  1999-04-01       Impact factor: 11.361

5.  A distinct nuclear localization signal in the N terminus of Smad 3 determines its ligand-induced nuclear translocation.

Authors:  Z Xiao; X Liu; Y I Henis; H F Lodish
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-05       Impact factor: 11.205

6.  Structural basis for the functional difference between Smad2 and Smad3 in FAST-2 (forkhead activin signal transducer-2)-mediated transcription.

Authors:  R P Nagarajan; Y Chen
Journal:  Biochem J       Date:  2000-08-15       Impact factor: 3.857

7.  Different Smad2 partners bind a common hydrophobic pocket in Smad2 via a defined proline-rich motif.

Authors:  Rebecca A Randall; Stéphane Germain; Gareth J Inman; Paul A Bates; Caroline S Hill
Journal:  EMBO J       Date:  2002-01-15       Impact factor: 11.598

8.  Smad3 recruits the anaphase-promoting complex for ubiquitination and degradation of SnoN.

Authors:  S L Stroschein; S Bonni; J L Wrana; K Luo
Journal:  Genes Dev       Date:  2001-11-01       Impact factor: 11.361

9.  FoxH1 (Fast) functions to specify the anterior primitive streak in the mouse.

Authors:  P A Hoodless; M Pye; C Chazaud; E Labbé; L Attisano; J Rossant; J L Wrana
Journal:  Genes Dev       Date:  2001-05-15       Impact factor: 11.361

10.  The transcription factor FoxH1 (FAST) mediates Nodal signaling during anterior-posterior patterning and node formation in the mouse.

Authors:  M Yamamoto; C Meno; Y Sakai; H Shiratori; K Mochida; Y Ikawa; Y Saijoh; H Hamada
Journal:  Genes Dev       Date:  2001-05-15       Impact factor: 11.361

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