Signal transduction - Mad about SMADs

被引:49
作者
Wrana, J
Pawson, T
机构
[1] HOSP SICK CHILDREN,DIV GASTROENTEROL,TORONTO,ON M5G 1X8,CANADA
[2] MT SINAI HOSP,SAMUEL LUNENFELD RES INST,PROGRAM MOL BIOL & CANC,TORONTO,ON M5G 1X8,CANADA
关键词
D O I
10.1038/40290
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Signalling through the transforming growth factor-beta (TGF-beta) requires the so-called Smad proteins, and two papers now show how the Smads work. TGF-beta binds to its receptor, which then activates Smad2 to form a transcriptionally active complex with Smad4. But the crystal structure of Smad4 shows that its carboxy-terminal domain can join up with its amino-terminal domain, to prevent the formation of a complex and, hence, to inhibit TGF-beta- mediated signalling.
引用
收藏
页码:28 / 29
页数:2
相关论文
共 9 条
[1]   A transcriptional partner for MAD proteins in TGF-beta signalling [J].
Chen, X ;
Rubock, MJ ;
Whitman, M .
NATURE, 1996, 383 (6602) :691-696
[2]   MADR2 maps to 18q21 and encodes a TGF beta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma [J].
Eppert, K ;
Scherer, SW ;
Ozcelik, H ;
Pirone, R ;
Hoodless, P ;
Kim, H ;
Tsui, LC ;
Bapat, B ;
Gallinger, S ;
Andrulis, IL ;
Thomsen, GH ;
Wrana, JL ;
Attisano, L .
CELL, 1996, 86 (04) :543-552
[3]   DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1 [J].
Hahn, SA ;
Schutte, M ;
Hoque, ATMS ;
Moskaluk, CA ;
daCosta, LT ;
Rozenblum, E ;
Weinstein, CL ;
Fischer, A ;
Yeo, CJ ;
Hruban, RH ;
Kern, SE .
SCIENCE, 1996, 271 (5247) :350-353
[4]   Mutations increasing autoinhibition inactivate tumour suppressors Smad2 and Smad4 [J].
Hata, A ;
Lo, RS ;
Wotton, D ;
Lagna, G ;
Massague, J .
NATURE, 1997, 388 (6637) :82-87
[5]   MADR1, a MAD-related protein that functions in BMP2 signaling pathways [J].
Hoodless, PA ;
Haerry, T ;
Abdollah, S ;
Stapleton, M ;
OConnor, MB ;
Attisano, L ;
Wrana, JL .
CELL, 1996, 85 (04) :489-500
[6]   Partnership between DPC4 and SMAD proteins in TGF-beta signalling pathways [J].
Lagna, G ;
Hata, A ;
HemmatiBrivanlou, A ;
Massague, J .
NATURE, 1996, 383 (6603) :832-836
[7]   MADR2 is a substrate of the TGF beta receptor and its phosphorylation is required for nuclear accumulation and signaling [J].
MaciasSilva, M ;
Abdollah, S ;
Hoodless, PA ;
Pirone, R ;
Attisano, L ;
Wrana, JL .
CELL, 1996, 87 (07) :1215-1224
[8]   A structural basis for mutational inactivation of the tumour suppressor Smad4 [J].
Shi, YG ;
Hata, A ;
Lo, RS ;
Massague, J ;
Pavletich, NP .
NATURE, 1997, 388 (6637) :87-93
[9]   Receptor-associated Mad homologues synergize as effectors of the TGF-beta response [J].
Zhang, Y ;
Feng, XH ;
Wu, RY ;
Derynck, R .
NATURE, 1996, 383 (6596) :168-172