Expression of Sox transcription factors in the developing mouse pancreas

被引:108
作者
Lioubinski, O
Müller, M
Wegner, M
Sander, M
机构
[1] Zentrum Mol Neurobiol, Hamburg, Germany
[2] Univ Erlangen Nurnberg, Inst Biochem, Erlangen, Germany
关键词
Sox; transcription factor; mouse; pancreas; islet; development; embryo; insulin; glucagon;
D O I
10.1002/dvdy.10311
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
Previous work has identified members of the homeodomain and basic helix-loop-helix families of transcription factors as critical determinants of mammalian pancreatic development. Here, we describe the identification of HMG-box transcription factors of the Sox gene family in the mouse pancreas. We detected transcripts for Sox11, Sox4, Sox13, Sox5, Sox9, Sox8, Sox10, Sox7, Sox17, Sox18, Sox15, and Sox30 in embryonic pancreas and found Sox4, Sox9, and Sox13 in adult pancreatic islets. Expression of seven of these Sox factors was studied in more detail by in situ hybridization from the stage of early pancreatic outgrowth to birth. Expression of Sox11 was found in the mesenchyme surrounding the pancreatic buds, whereas Sox4 and Sox9 were confined to the pancreatic epithelium and later to islets. Sox13 and L-Sox5 showed expression in most of the pancreatic epithelial cells between embryonic days 12.5 and 14.5. Sox8 and Sox10 were detected in a thin layer of cells surrounding the islets. The expression patterns of Sox genes in the embryonic pancreas suggest that they could have important and possibly redundant functions in pancreas development. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:402 / 408
页数:7
相关论文
共 32 条
[1]   SOX8 expression during chick embryogenesis [J].
Bell, KM ;
Western, PS ;
Sinclair, AH .
MECHANISMS OF DEVELOPMENT, 2000, 94 (1-2) :257-260
[2]  
Bhushan A, 2001, DEVELOPMENT, V128, P5109
[3]   The transcription factor Sox10 is a key regulator of peripheral glial development [J].
Britsch, S ;
Goerich, DE ;
Riethmacher, D ;
Peirano, RI ;
Rossner, M ;
Nave, KA ;
Birchmeier, C ;
Wegner, M .
GENES & DEVELOPMENT, 2001, 15 (01) :66-78
[4]   A crucial component of the endoderm formation pathway, CASANOVA, is encoded by a novel sox-related gene [J].
Dickmeis, T ;
Mourrain, P ;
Saint-Etienne, L ;
Fischer, N ;
Aanstad, P ;
Clark, M ;
Strähle, U ;
Rosa, F .
GENES & DEVELOPMENT, 2001, 15 (12) :1487-1492
[5]   Transcribing pancreas [J].
Edlund, H .
DIABETES, 1998, 47 (12) :1817-1823
[6]   Role for FGFR2IIIb-mediated signals in controlling pancreatic endocrine progenitor cell proliferation [J].
Elghazi, L ;
Cras-Méneur, C ;
Czernichow, P ;
Scharfmann, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3884-3889
[7]  
Gittes GK, 1996, DEVELOPMENT, V122, P439
[8]   EPITHELIOMESENCHYMAL INTERACTION IN PANCREATIC MORPHOGENESIS [J].
GOLOSOW, N ;
GROBSTEIN, C .
DEVELOPMENTAL BIOLOGY, 1962, 4 (02) :242-&
[9]   Restricted expression of a novel murine atonal-related bHLH protein in undifferentiated neural precursors [J].
Gradwohl, G ;
Fode, C ;
Guillemot, F .
DEVELOPMENTAL BIOLOGY, 1996, 180 (01) :227-241
[10]   Direct lineage tracing reveals the ontogeny of pancreatic cell fates during mouse embryogenesis [J].
Gu, GQ ;
Brown, JR ;
Melton, DA .
MECHANISMS OF DEVELOPMENT, 2003, 120 (01) :35-43