PURIFICATION OF A GROUP OF HELA NUCLEAR PROTEINS THAT BIND TO A REGULATORY ELEMENT (-1430/-1327) OF THE HUMAN PROLIFERATING CELL NUCLEOLAR PROTEIN P120 GENE

被引:6
作者
CHATTERJEE, A [1 ]
BUSCH, RK [1 ]
JUNG, D [1 ]
ZHANG, WW [1 ]
BUSCH, H [1 ]
机构
[1] BAYLOR COLL MED,DEPT PHARMACOL,HOUSTON,TX 77030
关键词
D O I
10.1016/S0006-291X(05)81136-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A group of proteins was purified from HeLa nuclear extract by DNA affinity chromatography which bind to an important regulatory element (-1430/-1327) of the P120 gene. The DNA binding activity was enriched 1075 fold. By silver staining three major polypeptides (50, 40, 37 kDa) were detected in the purified fraction. The band shift assay and the southwestern assay showed that the 50 kDa protein (P50) binds to the F1 (-1430/-1327) DNA fragment. The binding specificity of the group of proteins with F1 DNA in the presence of non-specific competitor DNA is much higher than that of P50 alone. On the basis of molecular weight and specific antibody binding, the 37 kDa protein appears to be the B23 nucleolar protein. © 1991 Academic Press, Inc.
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页码:805 / 812
页数:8
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