Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice

Malgorzata E. Quinn, Allison Haaning, Stephanie Ware

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Limb anomalies are important birth defects that are incompletely understood genetically and mechanistically. GLI3, a mediator of hedgehog signaling, is a genetic cause of limb malformations including pre- and postaxial polydactyly, Pallister-Hall syndrome and Greig cephalopolysyndactyly. A closely related Gli (glioma-associated oncogene homolog)-superfamily member, ZIC3, causes X-linked heterotaxy syndrome in humans but has not been investigated in limb development. During limb development, post-translational processing of Gli3 from activator to repressor antagonizes and posteriorly restricts Sonic hedgehog (Shh). We demonstrate that Zic3 and Gli3 expression overlap in developing limbs and that Zic3 converts Gli3 from repressor to activator in vitro. In Gli3 mutant mice, Zic3 loss of function abrogates ectopic Shh expression in anterior limb buds, limits overexpression in the zone of polarizing activity and normalizes aberrant Gli3 repressor/Gli3 activator ratios observed in Gli3+/- embryos. Zic3 null;Gli3+/- neonates show rescue of the polydactylous phenotype seen in Gli3+/- animals. These studies identify a previously unrecognized role for Zic3 in regulating limb digit number via its modifying effect on Gli3 and Shh expression levels. Together, these results indicate that two Gli superfamily members that cause disparate human congenital malformation syndromes interact genetically and demonstrate the importance of Zic3 in regulating Shh pathway in developing limbs.

Original languageEnglish (US)
Article numberdds002
Pages (from-to)1888-1896
Number of pages9
JournalHuman Molecular Genetics
Volume21
Issue number8
DOIs
StatePublished - Apr 2012
Externally publishedYes

Fingerprint

Polydactyly
Haploinsufficiency
Hedgehogs
Extremities
Pallister-Hall Syndrome
Heterotaxy Syndrome
Limb Buds
Oncogenes
Glioma
Embryonic Structures
Phenotype

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)
  • Molecular Biology

Cite this

Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice. / Quinn, Malgorzata E.; Haaning, Allison; Ware, Stephanie.

In: Human Molecular Genetics, Vol. 21, No. 8, dds002, 04.2012, p. 1888-1896.

Research output: Contribution to journalArticle

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