The p53-induced factor Ei24 inhibits nuclear import through an importin β-binding-like domain.

Citation data:

The Journal of cell biology, ISSN: 1540-8140, Vol: 205, Issue: 3, Page: 301-12

Publication Year:
2014
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Citations 9
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Repository URL:
https://jdc.jefferson.edu/bmpfp/77
PMID:
24821838
DOI:
10.1083/jcb.201304055
PMCID:
PMC4018778
Author(s):
Lieu, Kim G; Shim, Eun-Hee; Wang, Jinling; Lokareddy, Ravi K; Tao, Tao; Cingolani, Gino; Zambetti, Gerard P; Jans, David A
Publisher(s):
Rockefeller University Press
Tags:
Biochemistry, Genetics and Molecular Biology; Department of Biochemistry and Molecular Biology; Thomas Jefferson University; importin (IMP) family; nuclear transporters; p53-induced factor Ei24; Other Medical Specialties
article description
The etoposide-induced protein Ei24 was initially identified as a p53-responsive, proapoptotic factor, but no clear function has been described. Here, we use a nonbiased proteomics approach to identify members of the importin (IMP) family of nuclear transporters as interactors of Ei24 and characterize an IMPβ-binding-like (IBBL) domain within Ei24. We show that Ei24 can bind specifically to IMPβ1 and IMPα2, but not other IMPs, and use a mutated IMPβ1 derivative to show that Ei24 binds to the same site on IMPβ1 as the IMPα IBB. Ectopic expression of Ei24 reduced the extent of IMPβ1- or IMPα/β1-dependent nuclear protein import specifically, whereas specific alanine substitutions within the IBBL abrogated this activity. Induction of endogenous Ei24 expression through etoposide treatment similarly inhibited nuclear import in a mouse embryonic fibroblast model. Thus, Ei24 can bind specifically to IMPβ1 and IMPα2 to impede their normal role in nuclear import, shedding new light on the cellular functions of Ei24 and its tumor suppressor role.