P68 RNA helicase is a nucleocytoplasmic shuttling protein
نویسندگان
چکیده
منابع مشابه
Identification of a Novel Nucleocytoplasmic Shuttling RNA Helicase of Trypanosomes
Gene expression in trypanosomes is controlled mostly by post-transcriptional pathways. Little is known about the components of mRNA nucleocytoplasmic export routes in these parasites. Comparative genomics has shown that the mRNA transport pathway is the least conserved pathway among eukaryotes. Nonetheless, we identified a RNA helicase (Hel45) that is conserved across eukaryotes and similar to ...
متن کاملThe POU protein Oct-6 is a nucleocytoplasmic shuttling protein
Like many POU domain proteins, Oct-6 plays important roles during vertebrate development. In accord with its function as a transcriptional regulator during neurogenesis and myelination, Oct-6 is predominantly found in the nucleus. Nuclear import is mediated by a nuclear localization signal at the N-terminal end of the POU homeodomain. Here we show, that Oct-6 in addition contains a nuclear expo...
متن کاملThe Nucleocytoplasmic Shuttling Functions of P68 in Cancer Cell Migration and Proliferation
P68 RNA helicase (p68), as a DEAD family protein, is a typical RNA helicase protein. P68 functions in many other biological processes, which include the regulations of the gene transcription, cell proliferation and cell differentiation. In our group, Y593 phosphorylated p68 was found to have a function in the epithelial mesynchymal transition, which is an important process for cancer metastasis...
متن کاملP68 RNA helicase as a molecular target for cancer therapy
The DEAD-box family of RNA helicase is known to be required in virtually all cellular processes involving RNA, and p68 is a prototypic one of the family. Reports have indicated that in addition to ATPase and RNA helicase ability, p68 can also function as a co-activator for transcription factors such as estrogen receptor alpha, tumor suppressor p53 and beta-catenin. More than that, post-translat...
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ژورنال
عنوان ژورنال: Cell Research
سال: 2009
ISSN: 1001-0602,1748-7838
DOI: 10.1038/cr.2009.113