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Publication : Distinct targeting pathways for the membrane insertion of tail-anchored (TA) proteins.

First Author  Favaloro V Year  2008
Journal  J Cell Sci Volume  121
Issue  11 Pages  1832-40
PubMed ID  18477612 Mgi Jnum  J:139779
Mgi Id  MGI:3810042 Doi  10.1242/jcs.020321
Citation  Favaloro V, et al. (2008) Distinct targeting pathways for the membrane insertion of tail-anchored (TA) proteins. J Cell Sci 121(Pt 11):1832-40
abstractText  Tail-anchored (TA) proteins are characterised by a C-terminal transmembrane region that mediates post-translational insertion into the membrane of the endoplasmic reticulum (ER). We have investigated the requirements for membrane insertion of three TA proteins, RAMP4, Sec61beta and cytocrome b5. We show here that newly synthesised RAMP4 and Sec61beta can accumulate in a cytosolic, soluble complex with the ATPase Asna1 before insertion into ER-derived membranes. Membrane insertion of these TA proteins is stimulated by ATP, sensitive to redox conditions and blocked by alkylation of SH groups by N-ethylmaleimide (NEM). By contrast, membrane insertion of cytochrome b5 is not found to be mediated by Asna1, not stimulated by ATP and not affected by NEM or an oxidative environment. The Asna1-mediated pathway of membrane insertion of RAMP4 and Sec61beta may relate to functions of these proteins in the ER stress response.
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