Global expression analysis of gene regulatory pathways during endocrine pancreatic development

被引:199
作者
Gu, GQ
Wells, JM
Dombkowski, D
Preffer, F
Aronow, B
Melton, DA [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Massachusetts Gen Hosp, Dept Pathol, Charlestown, MA 02129 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 01期
关键词
Myt1; endoderm; pancreas; endocrine; islets; microarray;
D O I
10.1242/dev.00921
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To define genetic pathways that regulate development of the endocrine pancreas, we generated transcriptional profiles of enriched cells isolated from four biologically significant stages of endocrine pancreas development: endoderm before pancreas specification, early pancreatic progenitor cells, endocrine progenitor cells and adult islets of Langerhans. These analyses implicate new signaling pathways in endocrine pancreas development, and identified sets of known and novel genes that are temporally regulated, as well as genes that spatially define developing endocrine cells from their neighbors. The differential expression of several genes from each time point was verified by RT-PCR and in situ hybridization. Moreover, we present preliminary functional evidence suggesting that one transcription factor encoding gene (Myt1), which was identified in our screen, is expressed in endocrine progenitors and may regulate alpha, beta and delta cell development. In addition to identifying new genes that regulate endocrine cell fate, this global gene expression analysis has uncovered informative biological trends that occur during endocrine differentiation.
引用
收藏
页码:165 / 179
页数:15
相关论文
共 64 条
[31]  
Kim SK, 1997, COLD SPRING HARB SYM, V62, P377
[32]   Intercellular signals regulating pancreas development and function [J].
Kim, SK ;
Hebrok, M .
GENES & DEVELOPMENT, 2001, 15 (02) :111-127
[33]   Induction of pancreatic differentiation by signals from blood vessels [J].
Lammert, E ;
Cleaver, O ;
Melton, D .
SCIENCE, 2001, 294 (5542) :564-567
[34]   Differentiation of embryonic stem cells to insulin-secreting structures similar to pancreatic islets [J].
Lumelsky, N ;
Blondel, O ;
Laeng, P ;
Velasco, I ;
Ravin, R ;
McKay, R .
SCIENCE, 2001, 292 (5520) :1389-1394
[35]   β-cell death during progression to diabetes [J].
Mathis, D ;
Vence, L ;
Benoist, C .
NATURE, 2001, 414 (6865) :792-798
[36]   NZF-2b is a novel predominant form of mouse NZF-2/MyT1, expressed in differentiated neurons especially at higher levels in newly generated ones [J].
Matsushita, F ;
Kameyama, T ;
Marunouchi, T .
MECHANISMS OF DEVELOPMENT, 2002, 118 (1-2) :209-213
[37]  
Miralles F, 1998, DEVELOPMENT, V125, P1017
[38]   TGF-β plays a key role in morphogenesis of the pancreatic islets of Langerhans by controlling the activity of the matrix metalloproteinase MMP-2 [J].
Miralles, F ;
Battelino, T ;
Czernichow, P ;
Scharfmann, R .
JOURNAL OF CELL BIOLOGY, 1998, 143 (03) :827-836
[39]  
MOTRO B, 1991, DEVELOPMENT, V113, P1207
[40]   Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse [J].
Mukhopadhyay, M ;
Shtrom, S ;
Rodriguez-Esteban, C ;
Chen, L ;
Tsukui, T ;
Gomer, L ;
Dorward, DW ;
Glinka, A ;
Grinberg, A ;
Huang, SP ;
Niehrs, C ;
Belmonte, JCI ;
Westphal, H .
DEVELOPMENTAL CELL, 2001, 1 (03) :423-434