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PMID: 12198547 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Shh and Gli3 are dispensable for limb skeleton formation but regulate digit number and identity.

Nature ·Vol. 418 ·No. 6901 ·2002-08-29 ·Pages 979-83

Litingtung Y, Dahn RD, Li Y, Fallon JF, Chiang C

Abstract

Most current models propose Sonic hedgehog (Shh) as the primary determinant of anteroposterior development of amniote limbs. Shh protein is said to be required to direct the formation of skeletal elements and to specify digit identity through dose-dependent activation of target gene expression. However, the identity of genes targeted by Shh, and the regulatory mechanisms controlling their expression, remain poorly understood. Gli3 (the gene implicated in human Greig cephalopolysyndactyly syndrome) is proposed to negatively regulate Shh by restricting its expression and influence to the posterior mesoderm. Here we report genetic analyses in mice showing that Shh and Gli3 are dispensable for formation of limb skeletal elements: Shh(-/-) Gli3(-/-) limbs are distally complete and polydactylous, but completely lack wild-type digit identities. We show that the effects of Shh signalling on skeletal patterning and ridge maintenance are necessarily mediated through Gli3. We propose that the function of Shh and Gli3 in limb skeletal patterning is limited to refining autopodial morphology, imposing pentadactyl constraint on the limb's polydactyl potential, and organizing digit identity specification, by regulating the relative balance of Gli3 transcriptional activator and repressor activities.

MeSH Terms
Animals Blotting, Western Body Patterning DNA-Binding Proteins/genetics,metabolism Extremities/embryology,physiology Gene Deletion Gene Expression Regulation, Developmental Hedgehog Proteins In Situ Hybridization Kruppel-Like Transcription Factors Leg Bones/embryology,metabolism Limb Buds/embryology,metabolism Mice Mice, Knockout Morphogenesis Nerve Tissue Proteins RNA, Messenger/genetics,metabolism Signal Transduction Trans-Activators/genetics,metabolism Transcription Factors/genetics,metabolism Zinc Finger Protein Gli3
Chemicals
DNA-Binding Proteins Gli3 protein, mouse Hedgehog Proteins Kruppel-Like Transcription Factors Nerve Tissue Proteins RNA, Messenger Shh protein, mouse Trans-Activators Transcription Factors Zinc Finger Protein Gli3
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Litingtung Ying
Vanderbilt University Medical Center, Department of Cell and Developmental Biology, Nashville, Tennessee 37232, USA.
Dahn Randall D
Li Yina
Fallon John F
Chiang Chin
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
2002-08-29
Epub
2002-00-18
Pages
979-83
Language
English
Region
England
NLM ID
0410462
Subset
IM
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