ISOLATION AND CHARACTERIZATION OF THE HC8 SUBUNIT GENE OF THE HUMAN PROTEASOME

被引:10
作者
AKIOKA, H
FORSBERG, NE
ISHIDA, N
OKUMURA, K
NOGAMI, M
TAGUCHI, H
NODA, C
TANAKA, K
机构
[1] UNIV TOKUSHIMA,INST ENZYME RES,TOKUSHIMA 770,JAPAN
[2] OREGON STATE UNIV,DEPT ANIM SCI,CORVALLIS,OR 97331
[3] SANTEN PHARMACEUT CO LTD,CENT RES LABS,OSAKA 533,JAPAN
[4] MIE UNIV,FAC BIORESOURCES,TSU,MIE 514,JAPAN
关键词
D O I
10.1006/bbrc.1995.1190
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
For study of the molecular basis of regulation of proteasome gene expression, we isolated the gene encoding the alpha-type HC8 subunit of the human proteasome. About 2.3 kb of the 5' flanking region of this gene was tested for promoter function by chloramphenicol acetyltransferase assay. This analysis revealed that CAAT and TATA boxes, but not a GC box, are essential for its promoter activity. These results differed from previous findings that the genes for the alpha-type HC3 and beta-type HC5 subunits of the human proteasome have a TATA-less promoter and that two or three GC boxes function as the promoter sequences (Tamura, T. et al. (1994) J. Mel. Biol. 244, 1117-1124). We mapped the HC8 gene at q23 on human chromosome 14, which differs from the chromosomal locations of nine other proteasomal subunit genes mapped so far. (C) 1995 Academic Press, Inc.
引用
收藏
页码:318 / 323
页数:6
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