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PMID: 14660441 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Global expression analysis of gene regulatory pathways during endocrine pancreatic development.

Development (Cambridge, England) ·Vol. 131 ·No. 1 ·2004-01-00 ·Pages 165-79

Gu G, Wells JM, Dombkowski D, Preffer F, Aronow B, Melton DA

Abstract

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.

MeSH Terms
Animals Cell Differentiation/genetics,physiology DNA-Binding Proteins Embryonic and Fetal Development/genetics Female Gene Expression Regulation, Developmental/physiology Green Fluorescent Proteins In Situ Hybridization Islets of Langerhans/cytology,embryology,growth & development Luminescent Proteins/genetics Mice Mice, Inbred ICR Mice, Transgenic Pregnancy Protein Serine-Threonine Kinases/genetics Protein-Tyrosine Kinases/genetics Reverse Transcriptase Polymerase Chain Reaction Transcription Factors Transcription, Genetic
Chemicals
DNA-Binding Proteins Luminescent Proteins MYT1 protein, human Transcription Factors Green Fluorescent Proteins Protein-Tyrosine Kinases Protein Serine-Threonine Kinases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Gu Guoqiang
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Wells James M
Dombkowski David
Preffer Fred
Aronow Bruce
Melton Douglas A
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2004-01-00
Epub
2003-00-03
Pages
165-79
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIDDK NIH HHS · F32 DK009832 · United States
NIDDK NIH HHS · R01 DK065949 · United States
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