Protease-dependent defects in N-cadherin processing drive PMM2-CDG pathogenesis

Elsenoor J. Klaver, Lynn Dukes-Rimsky, Brijesh Kumar, Zhi Jie Xia, Tammie Dang, Mark A. Lehrman, Peggi Angel, Richard R. Drake, Hudson H. Freeze, Richard Steet, Heather Flanagan-Steet

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

The genetic bases for the congenital disorders of glycosylation (CDG) continue to expand, but how glycosylation defects cause patient phenotypes remains largely unknown. Here, we combined developmental phenotyping and biochemical studies in a potentially new zebrafish model (pmm2sa10150) of PMM2-CDG to uncover a protease-mediated pathogenic mechanism relevant to craniofacial and motility phenotypes in mutant embryos. Mutant embryos had reduced phosphomannomutase activity and modest decreases in N-glycan occupancy as detected by matrix-assisted laser desorption ionization mass spectrometry imaging. Cellular analyses of cartilage defects in pmm2sa10150 embryos revealed a block in chondrogenesis that was associated with defective proteolytic processing, but seemingly normal N-glycosylation, of the cell adhesion molecule N-cadherin. The activities of the proconvertases and matrix metalloproteinases responsible for N-cadherin maturation were significantly altered in pmm2sa10150 mutant embryos. Importantly, pharmacologic and genetic manipulation of proconvertase activity restored matrix metalloproteinase activity, N-cadherin processing, and cartilage pathology in pmm2sa10150 embryos. Collectively, these studies demonstrate in CDG that targeted alterations in protease activity create a pathogenic cascade that affects the maturation of cell adhesion proteins critical for tissue development.

Original languageEnglish (US)
Article numbere153474
JournalJCI Insight
Volume6
Issue number24
DOIs
StatePublished - Dec 22 2021

ASJC Scopus subject areas

  • General Medicine

Fingerprint

Dive into the research topics of 'Protease-dependent defects in N-cadherin processing drive PMM2-CDG pathogenesis'. Together they form a unique fingerprint.

Cite this