Sonic hedgehog mutations identified in holoprosencephaly patients can act in a dominant negative manner

Samer Singh, Robert Tokhunts, Valerie Baubet, John A. Goetz, Zhen Jane Huang, Neal S. Schilling, Kendall E. Black, Todd A. MacKenzie, Nadia Dahmane, David J. Robbins

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

Sonic hedgehog (SHH) plays an important instructional role in vertebrate development, as exemplified by the numerous developmental disorders that occur when the SHH pathway is disrupted. Mutations in the SHH gene are the most common cause of sporadic and inherited holoprosencephaly (HPE), a developmental disorder that is characterized by defective prosencephalon development. SHH HPE mutations provide a unique opportunity to better understand SHH biogenesis and signaling, and to decipher its role in the development of HPE. Here, we analyzed a panel of SHH HPE missense mutations that encode changes in the amino-terminal active domain of SHH. Our results show that SHH HPE mutations affect SHH biogenesis and signaling at multiple steps, which broadly results in low levels of protein expression, defective processing of SHH into its active form and protein with reduced activity. Additionally, we found that some inactive SHH proteins were able to modulate the activity of wt SHH in a dominant negative manner, both in vitro and in vivo. These findings show for the first time the susceptibility of SHH driven developmental processes to perturbations by low-activity forms of SHH. In conclusion, we demonstrate that SHH mutations found in HPE patients affect distinct steps of SHH biogenesis to attenuate SHH activity to different levels, and suggest that these variable levels of SHH activity might contribute to some of the phenotypic variation found in HPE patients.

Original languageEnglish (US)
Pages (from-to)95-103
Number of pages9
JournalHuman genetics
Volume125
Issue number1
DOIs
StatePublished - Jan 1 2009
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Singh, S., Tokhunts, R., Baubet, V., Goetz, J. A., Huang, Z. J., Schilling, N. S., Black, K. E., MacKenzie, T. A., Dahmane, N., & Robbins, D. J. (2009). Sonic hedgehog mutations identified in holoprosencephaly patients can act in a dominant negative manner. Human genetics, 125(1), 95-103. https://doi.org/10.1007/s00439-008-0599-0