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

Author

Listed:
  • Ying Litingtung

    (Vanderbilt University Medical Center)

  • Randall D. Dahn

    (University of Wisconsin)

  • Yina Li

    (Vanderbilt University Medical Center)

  • John F. Fallon

    (University of Wisconsin)

  • Chin Chiang

    (Vanderbilt University Medical Center)

Abstract

Most current models propose Sonic hedgehog (Shh) as the primary determinant of anteroposterior development of amniote limbs1. 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 mesoderm2,3,4. 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.

Suggested Citation

  • Ying Litingtung & Randall D. Dahn & Yina Li & John F. Fallon & Chin Chiang, 2002. "Shh and Gli3 are dispensable for limb skeleton formation but regulate digit number and identity," Nature, Nature, vol. 418(6901), pages 979-983, August.
  • Handle: RePEc:nat:nature:v:418:y:2002:i:6901:d:10.1038_nature01033
    DOI: 10.1038/nature01033
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    Cited by:

    1. Adrian On Wah Leung & Andrew Chung Hin Poon & Xue Wang & Chen Feng & Peikai Chen & Zhengfan Zheng & Michael KaiTsun To & Wilson Cheuk Wing Chan & Martin Cheung & Danny Chan, 2024. "Suppression of apoptosis impairs phalangeal joint formation in the pathogenesis of brachydactyly type A1," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    2. González-Forero, Mauricio, 2024. "A mathematical framework for evo-devo dynamics," Theoretical Population Biology, Elsevier, vol. 155(C), pages 24-50.
    3. Rachel K. Lex & Weiqiang Zhou & Zhicheng Ji & Kristin N. Falkenstein & Kaleigh E. Schuler & Kathryn E. Windsor & Joseph D. Kim & Hongkai Ji & Steven A. Vokes, 2022. "GLI transcriptional repression is inert prior to Hedgehog pathway activation," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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