Regulation of MAP kinase by the BMP-4/TAK1 pathway in Xenopus ectoderm

被引:48
作者
Goswami, M [1 ]
Uzgare, AR [1 ]
Sater, AK [1 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Houston, TX 77204 USA
基金
美国国家科学基金会;
关键词
MAP kinase; BMP-4; TAK1; neural induction; epidermis; FGF; gastrula; embryo; Xenopus;
D O I
10.1006/dbio.2001.0338
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Bone morphogenetic protein-4 (BMP-4) induces epidermis and represses neural fate in Xenopus ectoderm. Our previous findings implicate p42 Erk MAP kinase (MAPK) in the response to neural induction. We have examined the effects of BMP-4 on MAPK activity in gastrula ectoderm. Expression of a dominant negative BMP-4 receptor resulted in a 4.5-fold elevation in MAPK activity in midgastrula ectoderm. MAPK activity was reduced in ectoderm expressing a constitutively active BMP-4 receptor, or ectoderm treated with BMP-4 protein in the presence or absence of cycloheximide. Overexpression of TAK1 led to a reduction in MAPK activity in early gastrula ectoderm. The inhibitory effects of TAK1 could be reversed by 1 muM SB 203580, a p38 inhibitor. Treatment of isolated ectoderm with SB 203580 led to expression of otx2, NCAM, and noggin. Western blot analyses indicated that the BMP-4 pathway does not activate JNKs in ectoderm. Our findings indicate that BMP-4 inhibits ectodermal MAPK activity through a TAK1/p38-type pathway. MAPK has been shown to inactivate Smad1. Thus, our results suggest that BMP-4 and MAPK pathways are mutually antagonistic in Xenopus ectoderm, and that interactions between these pathways may govern the choice between epidermal and neural fate. (C) 2001 Academic Press.
引用
收藏
页码:259 / 270
页数:12
相关论文
共 67 条
[1]
Alam J, 2000, J BIOL CHEM, V275, P27694
[2]
PD-098059 IS A SPECIFIC INHIBITOR OF THE ACTIVATION OF MITOGEN-ACTIVATED PROTEIN-KINASE KINASE IN-VITRO AND IN-VIVO [J].
ALESSI, DR ;
CUENDA, A ;
COHEN, P ;
DUDLEY, DT ;
SALTIEL, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27489-27494
[3]
Amthor H, 1999, DEVELOPMENT, V126, P1041
[4]
Evidence for a role of Rho-like GTPases and stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK) in transforming growth factor beta-mediated signaling [J].
Atfi, A ;
Djelloul, S ;
Chastre, E ;
Davis, RR ;
Gespach, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (03) :1429-1432
[5]
c-jun N-terminal kinase activation in Xenopus laevis eggs and embryos -: A possible non-genomic role for the JNK signaling pathway [J].
Bagowski, CP ;
Xiong, W ;
Ferrell, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1459-1465
[6]
Barron M, 2000, DEV DYNAM, V218, P383, DOI 10.1002/(SICI)1097-0177(200006)218:2<383::AID-DVDY11>3.0.CO
[7]
2-P
[8]
Transforming growth factor beta 1 inhibits mitogen-activated protein kinase induced by basic fibroblast growth factor in smooth muscle cells [J].
Berrou, E ;
FontenayRoupie, M ;
Quarck, R ;
McKenzie, FR ;
LevyToledano, S ;
Tobelem, G ;
Bryckaert, M .
BIOCHEMICAL JOURNAL, 1996, 316 :167-173
[9]
Regulation of glucose transport and glycogen synthesis in L6 muscle cells during oxidative stress - Evidence for cross-talk between the insulin and SAPK2/p38 mitogen-activated protein kinase signaling pathways [J].
Blair, AS ;
Hajduch, E ;
Litherland, GJ ;
Hundal, HS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36293-36299
[10]
Nlk is a murine protein kinase related to Erk/MAP kinases and localized in the nucleus [J].
Brott, BK ;
Pinsky, BA ;
Erikson, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (03) :963-968