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:2.5.1.18 (
glutathione S-transferase
)
22,582
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The latent nuclear antigen (LNA) of Kaposi's sarcoma-associated herpesvirus (KSHV) has an essential role in viral latent infection. LNA maintains the stability of KSHV episomes and modulates the expression of cellular genes. A novel cellular protein
KLIP1
was identified to interact with LNA through yeast two-hybrid screening, and confirmed by a
glutathione S-transferase
pull down assay. Domain mapping showed that
KLIP1
interacted with the N-terminal domain of LNA. Northern blot hybridization with a
KLIP1
probe identified a major transcript of 1.8 kb and a minor transcript of 2.8 kb. cDNA library screening and 5'-RACE revealed that the major transcript encoded an open-reading-frame of 1,257 bp and had a 5'-untranslated region of 73 nucleotides. The major
KLIP1
transcript was ubiquitously present in different cell types examined. A
KLIP1
synthetic peptide antibody detected a doublet of 58-kDa and 63-kDa proteins in a Western blot assay.
KLIP1
had two putative nuclear localization signals and showed punctate nuclear localization when expressed as a GFP-fusion protein.
KLIP1
interacted with LNA in vivo, as demonstrated by coimmunoprecipitation using KSHV-infected cells and colocalization when they were expressed as GFP- and DsRed-fusion proteins, respectively. Consistent with its interaction with LNA, nuclear localization, and possession of two leucine zipper motifs,
KLIP1
behaved like a transcriptional factor and repressed herpes simplex virus thymidine kinase (TK) promoter activity in a mammalian one-hybrid assay. In addition, cotransfection with LNA alleviated the transcriptional repression effect of
KLIP1
on TK promoter activity. These results suggest that
KLIP1
is a new member of cellular transcriptional repressors, and that LNA is involved in deregulating cellular transcription process.
...
PMID:Identification of a novel cellular transcriptional repressor interacting with the latent nuclear antigen of Kaposi's sarcoma-associated herpesvirus. 1294 84