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PMID: 16855389 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Control of murine kidney development by sonic hedgehog and its GLI effectors.

Cell cycle (Georgetown, Tex.) ·Vol. 5 ·No. 13 ·2006-07-00 ·Pages 1426-30

Gill PS, Rosenblum ND

Abstract

Sonic hedgehog (SHH) controls cell differentiation and morphogenesis in many tissues and species. The mammalian kidney is a paradigm for studying epithelial-mesenchymal interactions and growth factor signaling during embryogenesis. Here, we review our recent findings demonstrating that SHH is required for normal murine kidney development. During renal morphogenesis, SHH controls a hierarchy of genes including renal patterning genes, cell cycle modulators, and GLI family members. Our investigation of GLI protein processing and binding of GLI activators and repressor to SHH target genes provide insight into the molecular mechanisms by which SHH and its GLI family of effectors control renal embryogenesis. Further, we highlight the roles of BMP, WNT and FGF signaling during renal development and discuss possible interactions of these pathways with SHH signaling.

MeSH Terms
Animals Gene Expression Regulation, Developmental Hedgehog Proteins/genetics,metabolism Humans Kidney/embryology,metabolism Kruppel-Like Transcription Factors/genetics,metabolism Mice Protein Binding Signal Transduction Zinc Finger Protein GLI1
Chemicals
Gli1 protein, mouse Hedgehog Proteins Kruppel-Like Transcription Factors Shh protein, mouse Zinc Finger Protein GLI1
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gill Paul S
Program in Developmental Biology, The Hospital for Sick Children, Toronto, Canada.
Rosenblum Norman D
Article Info
Journal
Cell cycle (Georgetown, Tex.)
Abbr.
Cell Cycle
ISSN
1551-4005
Published
2006-07-00
Epub
2006-00-01
Pages
1426-30
Language
English
Region
United States
NLM ID
101137841
Subset
IM
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