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: UMLS:C0019158 (
hepatitis
)
30,205
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The process of host factor-mediated nucleocytoplasmic transport is critical for diverse cellular events in eukaryotes and the life cycle of viruses. We have previously identified a chromosome region maintenance 1-independent nuclear export signal (NES) at the C terminus of the large form of
hepatitis
delta antigen (HDAg), designated NES(HDAg-L) that is required for the assembly of
hepatitis
delta virus (HDV) (C.-H. Lee et al., J. Biol. Chem. 276:8142-8148, 2001). To look for interacting proteins of the NES(HDAg-L), yeast two-hybrid screening was applied using the GAL4-binding domain fused to the NES(HDAg-L) as bait. Among the positive clones, one encodes a protein, designated
NESI
[NES(HDAg-L) interacting protein] that specifically interacted with the wild-type NES(HDAg-L) but not with the export/package-defective HDAg-L mutant, NES*(HDAg-L), in which Pro-205 has been replaced by Ala. Northern blot analysis revealed
NESI
as the gene product of a 1.9-kb endogenous mRNA transcript that is present predominantly in human liver tissue.
NESI
consists of 467 amino acid residues and bears a putative actin-binding site and a bipartite nuclear localization signal. Specific interaction between HDAg-L and
NESI
was further confirmed by coimmunoprecipitation and immunofluorescence staining. Overexpression of antisense
NESI
RNAs inhibited the expression of
NESI
and abolished HDAg-L-mediated nuclear export and assembly of HDV genomic RNA. These data indicate a critical role of
NESI
in the assembly of HDV through interaction with HDAg-L.
...
PMID:Novel nuclear export signal-interacting protein, NESI, critical for the assembly of hepatitis delta virus. 1595 56