RT Journal Article SR Electronic T1 Collagen has a unique SEC24 preference for efficient export from the endoplasmic reticulum JF bioRxiv FD Cold Spring Harbor Laboratory SP 2021.02.23.431880 DO 10.1101/2021.02.23.431880 A1 Chung-Ling Lu A1 Steven Ortmeier A1 Jon Brudvig A1 Tamara Moretti A1 Jacob Cain A1 Simeon A. Boyadjiev A1 Jill M. Weimer A1 Jinoh Kim YR 2021 UL http://biorxiv.org/content/early/2021/10/28/2021.02.23.431880.abstract AB SEC24 is mainly involved in cargo sorting during COPII vesicle assembly. There are four SEC24 paralogs (A to D) in mammals, which are classified into two subgroups (SEC24A/B and SEC24C/D). Pathological mutations in SEC24D cause osteogenesis imperfecta with craniofacial dysplasia in humans. sec24d mutant fish also recapitulate the phenotypes. Consistent with the skeletal phenotypes, the secretion of collagen was severely defective in mutant fish, emphasizing the importance of SEC24D in collagen secretion. However, SEC24D patient-derived fibroblasts show only a mild secretion phenotype, suggesting tissue-specificity in the secretion process. Using Sec24d KO mice and cultured cells, we show that SEC24A and SEC24B also contribute to ER export of procollagen. In contrast, fibronectin 1 requires either SEC24C or SEC24D for ER export. On the basis of our results, we propose that procollagen interacts with multiple SEC24 paralogs for efficient export from the ER, and that this is the basis for tissue-specific phenotypes resulting from SEC24 paralog deficiency.Competing Interest StatementThe authors have declared no competing interest.