Identification of phosphatases for Smad in the BMP/DPP pathway

被引:91
作者
Chen, HB [1 ]
Shen, JL [1 ]
Ip, YT [1 ]
Xu, L [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
关键词
bone morphogenctic protein; decapentaplegic; mothers against decapentaplegic; Smad; pyruvate dehydrogenase phosphatase;
D O I
10.1101/gad.1384706
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phosphorylation of the SSXS motif of Smads is critical in activating the transforming growth factor beta (TGF-beta) and bone morphogenetic protein (BMP) pathways. However, the phosphatase(s) involved in dephosphorylating and hence inactivating Smads remained elusive. Through RNA interference (RNAi)-based screening of serine/threonine phosphatases in Drosophila S2 cells, we identified pyruvate dehydrogenase phosphatase (PDP) to be required for dephosphorylation of Mothers against Decapentaplegic (MAD), a Drosophila Smad. Biochemical and genetic evidence suggest that PDP directly dephosphorylates MAD and inhibits signal transduction of Decapentaplegic (DPP). We show that the mammalian PDPs are important in dephosphorylation of BMP-activated Smad1 but not TGF-beta-activated Smad2 or Smad3. Thus, PDPs specifically inactivate Smads in the BMP/DPP pathway.
引用
收藏
页码:648 / 653
页数:6
相关论文
共 34 条
[1]   T beta RI phosphorylation of Smad2 on Ser(465) and Ser(467) is required for Smad2-Smad4 complex formation and signaling [J].
Abdollah, S ;
MaciasSilva, M ;
Tsukazaki, T ;
Hayashi, H ;
Attisano, L ;
Wrana, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :27678-27685
[2]   Signal transduction by the TGF-β superfamily [J].
Attisano, L ;
Wrana, JL .
SCIENCE, 2002, 296 (5573) :1646-1647
[3]   The structure and mechanism of protein phosphatases: Insights into catalysis and regulation [J].
Barford, D ;
Das, AK ;
Egloff, MP .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1998, 27 :133-164
[4]   A transcriptional partner for MAD proteins in TGF-beta signalling [J].
Chen, X ;
Rubock, MJ ;
Whitman, M .
NATURE, 1996, 383 (6602) :691-696
[5]   Use of double-stranded RNA interference in Drosophila cell lines to dissect signal transduction pathways [J].
Clemens, JC ;
Worby, CA ;
Simonson-Leff, N ;
Muda, M ;
Maehama, T ;
Hemmings, BA ;
Dixon, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6499-6503
[6]   Crystal structure of the protein serine/threonine phosphatase 2C at 2.0 angstrom resolution [J].
Das, AK ;
Helps, NR ;
Cohen, PTW ;
Barford, D .
EMBO JOURNAL, 1996, 15 (24) :6798-6809
[7]   Smads:: Transcriptional activators of TGF-β responses [J].
Derynck, R ;
Zhang, Y ;
Feng, XH .
CELL, 1998, 95 (06) :737-740
[8]   The repressor function of Snail is required for Drosophila gastrulation and is not replaceable by Escargot or Worniu [J].
Hemavathy, K ;
Hu, XD ;
Ashraf, SI ;
Small, SJ ;
Ip, YT .
DEVELOPMENTAL BIOLOGY, 2004, 269 (02) :411-420
[9]   Isoenzymes of pyruvate dehydrogenase phosphatase - DNA-derived amino acid sequences, expression, and regulation [J].
Huang, BL ;
Gudi, R ;
Wu, PF ;
Harris, RA ;
Hamilton, J ;
Popov, KM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) :17680-17688
[10]   Nucleocytoplasmic shuttling of Smads 2, 3, and 4 permits sensing of TGF-β receptor activity [J].
Inman, GJ ;
Nicolás, FJ ;
Hill, CS .
MOLECULAR CELL, 2002, 10 (02) :283-294