Genomic profiling of mixer and Sox17β targets during Xenopus endoderm development

被引:15
作者
Dickinson, K [1 ]
Leonard, J [1 ]
Baker, JC [1 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94062 USA
关键词
mixer; Sox17; endoderm; Xenopus; microarray; Xtwik2; Borg4; March8; Gpr4; Cxcr4;
D O I
10.1002/dvdy.20636
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The transcription factors Mixer and Sox17 beta have well-characterized roles in endoderm specification during Xenopus embryogenesis. In order to more thoroughly understand the mechanisms by which these endodermal regulators act, we expressed Mixer and Sox17 beta in naive ectodermal tissue and, using oligonucleotide-based microarrays, compared their genomic transcriptional profile to that of unaffected tissue. Using this approach, we identified 71 transcripts that are upregulated by Mixer or Sox17 beta, 63 of which have previously uncharacterized roles in endoderm development. Furthermore, an in situ hybridization screen using antisense probes for several of these clones identified six targets of Mixer and/or Sox17 beta that are expressed in the endoderm during gastrula stages, providing new and regional markers of the endoderm. Our results contribute further insight into the functions of Mixer and Sox17 beta and bring us closer to understanding at the molecular level the pathways that regulate endoderm development.
引用
收藏
页码:368 / 381
页数:14
相关论文
共 61 条
[31]   Model-based analysis of oligonucleotide arrays: Expression index computation and outlier detection [J].
Li, C ;
Wong, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :31-36
[32]   A genetic regulatory network for Xenopus mesendoderm formation [J].
Loose, M ;
Patient, R .
DEVELOPMENTAL BIOLOGY, 2004, 271 (02) :467-478
[33]   Proton-sensing G-protein-coupled receptors [J].
Ludwig, MG ;
Vanek, M ;
Guerini, D ;
Gasser, JA ;
Jones, CE ;
Junker, U ;
Hofstetter, H ;
Wolf, RM ;
Seuwen, K .
NATURE, 2003, 425 (6953) :93-98
[34]  
Lustig KD, 1996, DEVELOPMENT, V122, P4001
[35]   ISOLATION OF A NOVEL G-PROTEIN-COUPLED RECEPTOR (CPR4) LOCALIZED TO CHROMOSOME 19Q13.3 [J].
MAHADEVAN, MS ;
BAIRD, S ;
BAILLY, JE ;
SHUTLER, GG ;
SABOURIN, LA ;
TSILFIDIS, C ;
NEVILLE, CE ;
NARANG, M ;
KORNELUK, RG .
GENOMICS, 1995, 30 (01) :84-88
[36]   G-protein-coupled receptors and signaling networks: emerging paradigms [J].
Marinissen, MJ ;
Gutkind, JS .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (07) :368-376
[37]   Distribution analysis of human two pore domain potassium channels in tissues of the central nervous system and periphery [J].
Medhurst, AD ;
Rennie, G ;
Chapman, CG ;
Meadows, H ;
Duckworth, MD ;
Kelsell, RE ;
Gloger, II ;
Pangalos, MN .
MOLECULAR BRAIN RESEARCH, 2001, 86 (1-2) :101-114
[38]  
Moepps B, 2000, EUR J IMMUNOL, V30, P2924, DOI 10.1002/1521-4141(200010)30:10<2924::AID-IMMU2924>3.0.CO
[39]  
2-Y
[40]  
Murphy Philip M., 1996, Cytokine and Growth Factor Reviews, V7, P47, DOI 10.1016/1359-6101(96)00009-3