Synergistic efficacy of LBH and αB-crystallin through inhibiting transcriptional activities of p53 and p21
Author(s) -
Yun Deng,
Yongqing Li,
Xiongwei Fan,
Wuzhou Yuan,
Huaping Xie,
Xiaoyang Mo,
Yan Yan,
Junmei Zhou,
Yuequn Wang,
Xianli Ye,
Yongqi Wan,
Xiushan Wu
Publication year - 2010
Publication title -
bmb reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.511
H-Index - 77
eISSN - 1976-670X
pISSN - 1976-6696
DOI - 10.5483/bmbrep.2010.43.6.432
Subject(s) - psychological repression , transfection , immunoprecipitation , transcriptional regulation , transcription factor , gene , microbiology and biotechnology , transcription (linguistics) , crystallin , cytoplasm , complementary dna , cdna library , biology , chemistry , gene expression , genetics , linguistics , philosophy
LBH is a transcription factor as a candidate gene for CHD associated with partial trisomy 2p syndrome. To identify potential LBH-interacting partners, a yeast two-hybrid screen using LBH as a bait was performed with a human heart cDNA library. One of the clones identified encodes alphaB-crystallin. Co-immunoprecipitation and GST pull-down assays showed that LBH interacts with alphaB-crystallin, which is further confirmed by mammalian two-hybrid assays. Co-localization analysis showed that in COS-7 cells, alphaB-crystallin that is cytoplasmic alone, accumulates partialy in the nucleus when co-transfected with LBH. Transient transfection assays indicated that overexpression of LBH or alphaB-crystallin reduced the transcriptional activities of p53 and p21, respectively, Overexpression of both alphaB-crystallin and LBH together resulted in a stronger repression of the transcriptional activities of p21 and p53. These results showed that the interaction of LBH and alphaB-crystallin may inhibit synergistically the transcriptional regulation of p53 and p21.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom