The Zinc-finger factor Insm1 (IA-1) is essential for the development of pancreatic β cells and intestinal endocrine cells

被引:166
作者
Gierl, Mathias S. [1 ]
Karoulias, Nikolaos [1 ]
Wende, Hagen [1 ]
Strehle, Michael [1 ]
Birchmeier, Carmen [1 ]
机构
[1] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
关键词
Insm1; development; endocrine; intestine; mouse; pancreas;
D O I
10.1101/gad.381806
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pancreatic and intestinal primordia contain epithelial progenitor cells that generate many cell types. During development, specific programs of gene expression restrict the developmental potential of such progenitors and promote their differentiation. The Insm1 (insulinoma- associated 1, IA- 1) gene encodes a Zinc- finger factor that was discovered in an insulinoma cDNA library. We show that pancreatic and intestinal endocrine cells express Insm1 and require Insm1 for their development. In the pancreas of Insm1 mutant mice, endocrine precursors are formed, but only few insulin-positive beta cells are generated. Instead, endocrine precursor cells accumulate that express none of the pancreatic hormones. A similar change is observed in the development of intestine, where endocrine precursor cells are formed but do not differentiate correctly. A hallmark of endocrine cell differentiation is the accumulation of proteins that participate in secretion and vesicle transport, and we find many of the corresponding genes to be down- regulated in Insm1 mutant mice. Insm1 thus controls a gene expression program that comprises hormones and proteins of the secretory machinery. Our genetic analysis has revealed a key role of Insm1 in differentiation of pancreatic and intestinal endocrine cells.
引用
收藏
页码:2465 / 2478
页数:14
相关论文
共 57 条
[1]   β-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes [J].
Ahlgren, U ;
Jonsson, J ;
Jonsson, L ;
Simu, K ;
Edlund, H .
GENES & DEVELOPMENT, 1998, 12 (12) :1763-1768
[2]   Notch signalling controls pancreatic cell differentiation [J].
Apelqvist, Å ;
Li, H ;
Sommer, L ;
Beatus, P ;
Anderson, DJ ;
Honjo, T ;
de Angelis, MH ;
Lendahl, U ;
Edlund, H .
NATURE, 1999, 400 (6747) :877-881
[3]   MafB -: An activator of the glucagon gene expressed in developing islet α- and β-cells [J].
Artner, I ;
Le Lay, J ;
Hang, Y ;
Elghazi, L ;
Schisler, JC ;
Henderson, E ;
Sosa-Pineda, B ;
Stein, R .
DIABETES, 2006, 55 (02) :297-304
[4]   Diabetes mellitus and genetically programmed defects in β-cell function [J].
Bell, GI ;
Polonsky, KS .
NATURE, 2001, 414 (6865) :788-791
[5]   NeuroD1/E47 regulates the e-box element of a novel zinc finger transcription factor, IA-1, in developing nervous system [J].
Breslin, MB ;
Zhu, M ;
Lan, MS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (40) :38991-38997
[6]   Neuroendocrine differentiation factor, IA-1, is a transcriptional repressor and contains a specific DNA-binding domain: identification of consensus IA-1 binding sequence [J].
Breslin, MB ;
Zhu, M ;
Notkins, AL ;
Lan, MS .
NUCLEIC ACIDS RESEARCH, 2002, 30 (04) :1038-1045
[7]   The ErbB2 and ErbB3 receptors and their ligand, neuregulin-1, are essential for development of the sympathetic nervous system [J].
Britsch, S ;
Li, L ;
Kirchhoff, S ;
Theuring, F ;
Brinkmann, V ;
Birchmeier, C ;
Riethmacher, D .
GENES & DEVELOPMENT, 1998, 12 (12) :1825-1836
[8]   Targeting genes for self-excision in the germ line [J].
Bunting, M ;
Bernstein, KE ;
Greer, JM ;
Capecchi, MR ;
Thomas, KR .
GENES & DEVELOPMENT, 1999, 13 (12) :1524-1528
[9]   TEMPORAL AND SPATIAL PATTERNS OF TRANSGENE EXPRESSION IN AGING ADULT MICE PROVIDE INSIGHTS ABOUT THE ORIGINS, ORGANIZATION, AND DIFFERENTIATION OF THE INTESTINAL EPITHELIUM [J].
COHN, SM ;
ROTH, KA ;
BIRKENMEIER, EH ;
GORDON, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :1034-1038
[10]  
Collier Dawn C, 2003, J Appl Clin Med Phys, V4, P17, DOI 10.1120/1.1521271