The role of p58IPK in protecting the stressed endoplasmic reticulum.

Abstract:

:The preemptive quality control (pQC) pathway protects cells from acute endoplasmic reticulum (ER) stress by attenuating translocation of nascent proteins despite their targeting to translocons at the ER membrane. Here, we investigate the hypothesis that the DnaJ protein p58(IPK) plays an essential role in this process via HSP70 recruitment to the cytosolic face of translocons for extraction of translocationally attenuated nascent chains. Our analyses revealed that the heightened stress sensitivity of p58-/- cells was not due to an impairment of the pQC pathway or elevated ER substrate burden during acute stress. Instead, the lesion was in the protein processing capacity of the ER lumen, where p58(IPK) was found to normally reside in association with BiP. ER lumenal p58(IPK) could be coimmunoprecipitated with a newly synthesized secretory protein in vitro and stimulated protein maturation upon overexpression in cells. These results identify a previously unanticipated location for p58(IPK) in the ER lumen where its putative function as a cochaperone explains the stress-sensitivity phenotype of knockout cells and mice.

journal_name

Mol Biol Cell

authors

Rutkowski DT,Kang SW,Goodman AG,Garrison JL,Taunton J,Katze MG,Kaufman RJ,Hegde RS

doi

10.1091/mbc.e07-03-0272

subject

Has Abstract

pub_date

2007-09-01 00:00:00

pages

3681-91

issue

9

eissn

1059-1524

issn

1939-4586

pii

E07-03-0272

journal_volume

18

pub_type

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