Screening and Identification of The Proteins Interacting With NLS-RARα Protein
10.3724/SP.J.1206.2008.00424
- VernacularTitle:NLS-RARα蛋白相互作用蛋白的筛选与验证
- Author:
Chong WANG
;
Liang ZHONG
;
Dongsheng WANG
;
Beizhong LIU
;
Fei LIAO
;
Po HAO
;
Chang LIU
;
Danting JIN
;
Chunguang WANG
- Publication Type:Journal Article
- Keywords:
NLS-RARα protein;
leukemia;
yeast two-hybrid;
protein-protein interaction
- From:
Progress in Biochemistry and Biophysics
2009;36(4):500-505
- CountryChina
- Language:Chinese
-
Abstract:
Acute promyelocytic leukemia (APL) is characterized by the generation of the prototypic promyelocytic leukemia-retinoicacid receptor alpha (PML-RARα), an oncogenic fusion protein due to chromosomal translocation. In a human myeloid cell line,PML-RARα is cleaved by neutrophil elastase (NE) to produce the mutational PML [nuclear localization signal (NLS) deletion andRARα (NLS-RARα, containing NLS of PML), both of which may play an important role in APL pathogenesis. The yeast two-hybridtechnique was used to screen the intracellular proteins interacting with NLS-RARα, which may be involved in NLS-RARα signaling. The NLS-RARα coding sequence was amplified by polymerase chain reaction method and was cloned into the bait plasmid pGBKT7vector, which, after the confirmation by sequencing, was transformed into yeast AH109 and the subsequent expression of bait plasmidwas proved by Western-blot. The transformed yeast AH109 was mated with yeast Y187 (containing leukemia cDNA library plasmidspACT2) in medium. Diploid yeast was plated on synthetic dropout nutrient medium containing X-α-gal for screening. After beingreintroduced into yeast AH109 and sequenced to verify the expression of ORF, eight positive colonies were obtained, among whichonecontaining JTV-1 was cloned. The interaction between NLS-RARα and JTV-1 was further supported by indirect immunofluorescence,GST pull-down and co-immunoprecipitation, respectively. These findings brought some new clues for the further exploration ofNLS-RARα signaling to APL.
