| Literature DB >> 18314878 |
Monica Cattaneo1, Mieko Otsu, Claudio Fagioli, Simone Martino, Lavinia Vittoria Lotti, Roberto Sitia, Ida Biunno.
Abstract
When expressed in the absence of light chains, secretory Ig-micro chains (micro(s)) undergo endoplasmic reticulum associated degradation (ERAD). This process involves the recognition of terminally misfolded or unassembled molecules, their retro-translocation across the ER membrane and ubiquitination for degradation by cytosolic proteasomes. The molecular components of the ERAD pathway and their coordination remain largely unknown. Here we employed co-immunoprecipitation, silencing or over-expression assays to show that SEL1L and HRD1 are involved in the degradation of unassembled Ig-micro(s), but have minor effects on another substrate, TCR-alpha. SEL1L and HRD1 localize in the early secretory apparatus and are induced by ER stress and during B cell differentiation, concomitantly with the onset of massive IgM secretion. These findings reveal a role for SEL1L and HRD1 in IgM quality control. (c) 2008 Wiley-Liss, Inc.Entities:
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Year: 2008 PMID: 18314878 DOI: 10.1002/jcp.21364
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384