Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:1.3.5.1 (
succinate dehydrogenase
)
8,177
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Large coat protein
complex II
(COPII)-coated vesicles serve to convey the large cargo procollagen I (PC1) from the endoplasmic reticulum (ER). The link between large cargo in the lumen of the ER and modulation of the COPII machinery remains unresolved. TANGO1 is required for PC secretion and interacts with PC and COPII on opposite sides of the ER membrane, but evidence suggests that TANGO1 is retained in the ER, and not included in normal size (<100 nm) COPII vesicles. Here we show that TANGO1 is exported out of the ER in large COPII-coated PC1 carriers, and retrieved back to the ER by the retrograde coat, COPI, mediated by the C-terminal RDEL retrieval sequence of HSP47. TANGO1 is known to target the COPII initiation factor
SEC12
to ER exit sites through an interacting protein, cTAGE5.
SEC12
is important for the growth of COPII vesicles, but it is not sorted into small budded vesicles. We found both cTAGE5 and
SEC12
were exported with TANGO1 in large COPII carriers. In contrast to its exclusion from small transport vesicles,
SEC12
was particularly enriched around ER membranes and large COPII carriers that contained PC1. We constructed a split GFP system to recapitulate the targeting of
SEC12
to PC1 via the luminal domain of TANGO1. The minimal targeting system enriched
SEC12
around PC1 and generated large PC1 carriers. We conclude that TANGO1, cTAGE5, and
SEC12
are copacked with PC1 into COPII carriers to increase the size of COPII, thus ensuring the capture of large cargo.
...
PMID:TANGO1 and SEC12 are copackaged with procollagen I to facilitate the generation of large COPII carriers. 3054 19