Xenopus Xlmo4 is a GATA cofactor during ventral mesoderm formation and regulates Ldb1 availability at the dorsal mesoderm and the neural plate

被引:10
作者
de la Calle-Mustienes, E
Lu, ZX
Cortés, M
Andersen, B
Modolell, J
Gómez-Skarmeta, JL
机构
[1] CSIC, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, E-28049 Madrid, Spain
[3] Univ Calif Irvine, Dept Med, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
关键词
Xenopus; XLim-1; LMO4; ventral mesoderm; iroquois;
D O I
10.1016/j.ydbio.2003.09.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have identified and functionally characterized the Xenopus Xlmo4 gene, which encodes a member of the LIM-domain-only protein family. Xlmo4 is activated at gastrula stages in the mesodermal marginal zone probably in response to BMP4 signaling. Soon after, Xlmo4 is downregulated in the dorsal region of the mesoderm. This repression seems to be mediated by organizer-expressed repressors, such as Gsc. Xlmo4 downregulation is necessary for the proper formation of this territory. Increasing Xlmo4 function in this region downregulates Spemman Organizer genes and suppresses dorsal-anterior structures. By binding to Ldb1, Xlmo4 may restrict the availability of this cofactor for transcription factors expressed at the Spemman Organizer. In the ventral mesoderm, Xlmo4 is required to establish the identity of this territory by acting as a positive cofactor of GATA factors. In the neural ectoderm, Xlmo4 expression depends on Xiro homeoprotein activity. In this region, Xlmo4 suppresses differentiation of primary neurons and interferes with gene expression at the Isthmic Organizer, most likely by displacing Ldb1 from active transcription factor complexes required for these processes. Together, our data suggest that Xlmo4 uses distinct mechanisms to participate in different processes during development. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:564 / 581
页数:18
相关论文
共 63 条
[1]   RLIM inhibits functional activity of LIM homeodomain transcription factors via recruitment of the histone deacetylase complex [J].
Bach, I ;
Rodriguez-Esteban, C ;
Carrière, C ;
Bhushan, A ;
Krones, A ;
Rose, DW ;
Glass, CK ;
Andersen, B ;
Belmonte, JCI ;
Rosenfeld, MG .
NATURE GENETICS, 1999, 22 (04) :394-399
[2]   The LIM domain: regulation by association [J].
Bach, I .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :5-17
[3]   A family of LIM domain-associated cofactors confer transcriptional synergism between LIM and Otx homeodomain proteins [J].
Bach, I ;
Carriere, C ;
Ostendorff, HP ;
Andersen, B ;
Rosenfeld, MG .
GENES & DEVELOPMENT, 1997, 11 (11) :1370-1380
[4]  
Bao JX, 2000, DEVELOPMENT, V127, P425
[5]   Multiple functions of LIM domain-binding CLIM/NLI/Ldb cofactors during zebrafish development [J].
Becker, T ;
Ostendorff, HP ;
Bossenz, M ;
Schlüter, A ;
Becker, CG ;
Peirano, RI ;
Bach, I .
MECHANISMS OF DEVELOPMENT, 2002, 117 (1-2) :75-85
[6]   GATA factors and the origins of adult and embryonic blood in Xenopus: Responses to retinoic acid [J].
Bertwistle, D ;
Walmsley, ME ;
Read, EM ;
Pizzey, JA ;
Patient, RK .
MECHANISMS OF DEVELOPMENT, 1996, 57 (02) :199-214
[7]   Xiro homeoproteins coordinate cell cycle exit and primary neuron formation by upregulating neuronal-fate repressors and downregulating the cell-cycle inhibitor XGadd45-γ [J].
Calle-Mustienes, ED ;
Glavic, A ;
Modolell, J ;
Gómez-Skarmeta, JL .
MECHANISMS OF DEVELOPMENT, 2002, 119 (01) :69-80
[8]  
Cavodeassi F, 2001, DEVELOPMENT, V128, P2847
[9]   EXPRESSION OF AN EXTRACELLULAR DELETION OF XOTCH DIVERTS CELL FATE IN XENOPUS-EMBRYOS [J].
COFFMAN, CR ;
SKOGLUND, P ;
HARRIS, WA ;
KINTNER, CR .
CELL, 1993, 73 (04) :659-671
[10]   LIM domains: multiple roles as adapters and functional modifiers in protein interactions [J].
Dawid, IB ;
Breen, JJ ;
Toyama, R .
TRENDS IN GENETICS, 1998, 14 (04) :156-162