CDNA CLONING AND SEQUENCING OF COMPONENT C9 OF PROTEASOMES FROM RAT HEPATOMA-CELLS

被引:65
作者
KUMATORI, A
TANAKA, K
TAMURA, T
FUJIWARA, T
ICHIHARA, A
TOKUNAGA, F
ONIKURA, A
IWANAGA, S
机构
[1] UNIV TOKUSHIMA,INST ENZYME RES,TOKUSHIMA 770,JAPAN
[2] OTSUKA PHARMACEUT CO LTD,TOKUSHIMA 77101,JAPAN
[3] KYUSHU UNIV 33,GRAD SCH MED SCI,DEPT MOLEC BIOL,FUKUOKA 812,JAPAN
[4] KYUSHU UNIV 33,FAC SCI,DEPT BIOL,FUKUOKA 812,JAPAN
关键词
cDNA cloning; Multicatalytic proteinase; Proteasome; Subunit C9;
D O I
10.1016/0014-5793(90)80267-M
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 component C9 of rat proteasomes (multicatalytic proteinase complexes) has been determined from a recombinant cDNA clone isolated by screening a Reuber H4TG hepatoma cell cDNA library using synthetic oligodeoxynucleotide probes corresponding to partial amino acid sequences of the protein. The predicted sequence ofC9 consists of 261 amino acid residues with a calculated molecular weight of 29496. The C9 component is a novel protein, differing from known proteins, but its primary structure resembles those of other proteasome components, including C2, C3 and C5, although its similarity to C5 is relatively low, suggesting that proteasomes consist of a family of proteins that have evolved from a common ancestor. © 1990.
引用
收藏
页码:279 / 282
页数:4
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