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A PROTEIN-BINDING TO CARG BOX MOTIFS AND TO SINGLE-STRANDED-DNA FUNCTIONS AS A TRANSCRIPTIONAL REPRESSOR
被引:92
作者:
KAMADA, S
[1
]
MIWA, T
[1
]
机构:
[1] OSAKA UNIV,MICROBIAL DIS RES INST,DEPT ONCOGENE RES,3-1 YAMADAOKA,SUITA,OSAKA 565,JAPAN
来源:
关键词:
SMOOTH MUSCLE;
ACTIN;
TRANSCRIPTION FACTOR;
MOUSE;
LAMBDA-GT11;
LIBRARY;
REPRESSION;
RECOMBINANT DNA;
D O I:
10.1016/0378-1119(92)90276-U
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
A CArG box motif [CC(A+T-rich)6GG] is one of the DNA elements required for muscle-specific gene transcription. Nuclear factors in mouse C2 myogenic cells strongly bind to the CArG box in the first intron of the gene (Sm alpha-A) encoding human smooth muscle alpha-actin. To clone cDNAs of the CArG box-binding factor (CBF), lambdagt11 cDNA expression libraries from C2 cells were screened for in situ DNA binding specific for this CArG box sequence. The 1.6-kb cDNA (CBF-A) encoding 285 amino acids (aa) was obtained, and a beta-galactosidase fusion protein, bacterially produced from the cDNA, bound to DNA fragments containing several CArG boxes. When the expression level of CBF-A in C2 cells increased by transfection of CBF-A expression plasmids, Sm alpha-A transcription was repressed. The deduced aa sequence of CBF-A is similar to some single-stranded (ss) nucleic acid-binding proteins. The fusion protein could bind to ssDNA, whereas CBF in C2 cell nuclear extracts could not. From these results, CBF-A is a novel CArG box-, ssDNA- and RNA-binding protein, as well as a repressive transcriptional factor.
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页码:229 / 236
页数:8
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