Literature DB >> 9205116

Cloning and characterization of a novel member of the human Mad gene family (MADH6).

T K Watanabe1, M Suzuki, Y Omori, H Hishigaki, M Horie, N Kanemoto, T Fujiwara, Y Nakamura, E Takahashi.   

Abstract

MAD (mothers against decapentaplegic)-related proteins (MADRs) are intracellular components that play critical roles in signal-transduction pathways involving the transforming growth factor beta (TGFbeta) superfamily. Some Mad genes are candidates for tumor-suppressor functions. From a human fetal brain cDNA library we have isolated a novel Mad-related gene. Two alternatively transcribed mRNAs encode deduced 430- and 467-amino-acid peptides that showed high levels of similarity to MADR1/Smad1/hMAD1 (about 80% identity at the amino acid level). This gene, which we designated MADH6, resides on 13q12-q14 between BRCA2 and RB, a region that frequently displays loss of heterozygosity in breast, liver, and prostate cancers.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9205116     DOI: 10.1006/geno.1997.4753

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  11 in total

1.  Smad proteins exist as monomers in vivo and undergo homo- and hetero-oligomerization upon activation by serine/threonine kinase receptors.

Authors:  M Kawabata; H Inoue; A Hanyu; T Imamura; K Miyazono
Journal:  EMBO J       Date:  1998-07-15       Impact factor: 11.598

2.  Smad8 mediates the signaling of the ALK-2 [corrected] receptor serine kinase.

Authors:  Y Chen; A Bhushan; W Vale
Journal:  Proc Natl Acad Sci U S A       Date:  1997-11-25       Impact factor: 11.205

3.  The L3 loop: a structural motif determining specific interactions between SMAD proteins and TGF-beta receptors.

Authors:  R S Lo; Y G Chen; Y Shi; N P Pavletich; J Massagué
Journal:  EMBO J       Date:  1998-02-16       Impact factor: 11.598

4.  Identification and characterization of functional Smad8 and Smad4 homologues from Echinococcus granulosus.

Authors:  Chuanshan Zhang; Limin Wang; Hui Wang; Hongwei Pu; Le Yang; Jing Li; Junhua Wang; Guodong Lü; Xiaomei Lu; Wenbao Zhang; Dominique A Vuitton; Hao Wen; Renyong Lin
Journal:  Parasitol Res       Date:  2014-07-20       Impact factor: 2.289

5.  Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes.

Authors:  F Liu; C Pouponnot; J Massagué
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

6.  Positive and negative regulation of the transforming growth factor beta/activin target gene goosecoid by the TFII-I family of transcription factors.

Authors:  Manching Ku; Sergei Y Sokol; Jack Wu; Maria Isabel Tussie-Luna; Ananda L Roy; Akiko Hata
Journal:  Mol Cell Biol       Date:  2005-08       Impact factor: 4.272

7.  Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor.

Authors:  A Hata; G Lagna; J Massagué; A Hemmati-Brivanlou
Journal:  Genes Dev       Date:  1998-01-15       Impact factor: 11.361

8.  A maternal Smad protein regulates early embryonic apoptosis in Xenopus laevis.

Authors:  Yuko Miyanaga; Ingrid Torregroza; Todd Evans
Journal:  Mol Cell Biol       Date:  2002-03       Impact factor: 4.272

9.  The tumor suppressor SMAD4/DPC4 is essential for epiblast proliferation and mesoderm induction in mice.

Authors:  X Yang; C Li; X Xu; C Deng
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-31       Impact factor: 11.205

10.  Failure of egg cylinder elongation and mesoderm induction in mouse embryos lacking the tumor suppressor smad2.

Authors:  M Weinstein; X Yang; C Li; X Xu; J Gotay; C X Deng
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-04       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.