CDNA CLONING OF A NEW PUTATIVE ATPASE SUBUNIT P45 OF THE HUMAN 26S PROTEASOME, A HOMOLOG OF YEAST TRANSCRIPTIONAL FACTOR SUG1P

被引:61
作者
AKIYAMA, K
YOKOTA, K
KAGAWA, S
SHIMBARA, N
DEMARTINO, GN
SLAUGHTER, CA
NODA, C
TANAKA, K
机构
[1] UNIV TOKUSHIMA, INST ENZYME RES, TOKUSHIMA 770, JAPAN
[2] SCH MED TOKUSHIMA, DEPT UROL, TOKUSHIMA 770, JAPAN
[3] SUMITOMO ELECT IND LTD, DEPT BIOMED RES & DEV, SAKYO KU, YOKOHAMA, KANAGAWA 244, JAPAN
[4] UNIV TEXAS, SW MED CTR, DEPT PHYSIOL, DALLAS, TX 75235 USA
[5] UNIV TEXAS, SW MED CTR, HOWARD HUGHES MED INST, DALLAS, TX 75235 USA
[6] UNIV TEXAS, SW MED CTR, DEPT BIOCHEM, DALLAS, TX 75235 USA
来源
FEBS LETTERS | 1995年 / 363卷 / 1-2期
关键词
CDNA CLONING; 26S PROTEASOME; SUBUNIT P45; PUTATIVE ATPASE FAMILY; SUG1;
D O I
10.1016/0014-5793(95)00304-R
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
The nucleotide sequence of a cDNA that encodes a new regulatory subunit, named p45, of the 26S proteasome of human hepatoblastoma HepG2 cells has been determined. The polypeptide predicted from the open reading frame consists of 406 amino acid residues with a calculated molecular weight of 45770 and isoelectric point of 8.35. The sequences of several fragments of bovine p45, determined by protein chemical analyses, spanning 27% of the complete structure, were found to be in excellent accord with those deduced from the human cDNA sequence. Computer analysis showed that p45 belongs to a family of putative ATPases which includes regulatory components of 26S proteasomes. The overall structure of p45 was found to be homologous to that of yeast Sug1p, which has been identified as a transcripional factor. It is closely similar, but not identical to the sequence reported for Trip1, a functional homolog of Sug1p in human tissues. These results are consistent with the possibility that Sug1-like proteins with distinct sequence function in transcription and protein degradation in human cells. However, the alternative hypothesis, that the same gene locus encodes both p45 and Trip1, cannot be excluded on the basis of such closely similar sequences. In either case, both proteins are likely to function equivalently well in either transcription or protein degradation.
引用
收藏
页码:151 / 156
页数:6
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