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Scientific article
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The genetic basis of a craniofacial disease provides insight into COPII coat assembly

Published inDevelopmental cell, vol. 13, no. 5, p. 623-634
Publication date2007
Abstract

Proteins trafficking through the secretory pathway must first exit the endoplasmic reticulum (ER) through membrane vesicles created and regulated by the COPII coat protein complex. Cranio-lenticulo-sutural dysplasia (CLSD) was recently shown to be caused by a missense mutation in SEC23A, a gene encoding one of two paralogous COPII coat proteins. We now elucidate the molecular mechanism underlying this disease. In vitro assays reveal that the mutant form of SEC23A poorly recruits the Sec13-Sec31 complex, inhibiting vesicle formation. Surprisingly, this effect is modulated by the Sar1 GTPase paralog used in the reaction, indicating distinct affinities of the two human Sar1 paralogs for the Sec13-Sec31 complex. Patient cells accumulate numerous tubular cargo-containing ER exit sites devoid of observable membrane coat, likely representing an intermediate step in COPII vesicle formation. Our results indicate that the Sar1-Sec23-Sec24 prebudding complex is sufficient to form cargo-containing tubules in vivo, whereas the Sec13-Sec31 complex is required for membrane fission.

Keywords
  • Amino Acid Sequence
  • COP-Coated Vesicles/physiology
  • Carrier Proteins/metabolism
  • Cell Membrane/metabolism
  • Cells, Cultured
  • Craniofacial Abnormalities/genetics/metabolism/pathology
  • Endoplasmic Reticulum/physiology
  • Fibroblasts/physiology
  • Humans
  • Membrane Fusion
  • Models, Molecular
  • Molecular Sequence Data
  • Monomeric GTP-Binding Proteins/metabolism
  • Mutation
  • Osteoblasts/physiology
  • Protein Transport
  • Vesicular Transport Proteins/genetics/metabolism
Research group
Citation (ISO format)
FROMME, J Christopher et al. The genetic basis of a craniofacial disease provides insight into COPII coat assembly. In: Developmental cell, 2007, vol. 13, n° 5, p. 623–634. doi: 10.1016/j.devcel.2007.10.005
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Article (Published version)
accessLevelRestricted
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ISSN of the journal1534-5807
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