CDNA CLONING AND INTERFERON-GAMMA DOWN-REGULATION OF PROTEASOMAL SUBUNIT-X AND SUBUNIT-Y

被引:188
作者
AKIYAMA, KY
YOKOTA, KY
KAGAWA, S
SHIMBARA, N
TAMURA, T
AKIOKA, H
NOTHWANG, HG
NODA, C
TANAKA, K
ICHIHARA, A
机构
[1] UNIV TOKUSHIMA,INST ENZYME RES,TOKUSHIMA 770,JAPAN
[2] UNIV TOKUSHIMA,SCH MED,DEPT UROL,TOKUSHIMA 770,JAPAN
[3] SUMITOMO ELECT IND LTD,DEPT BIOMED RES & DEV,SAKAE KU,YOKOHAMA 244,JAPAN
关键词
D O I
10.1126/science.8066462
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proteasomes are the proteolytic complex responsible for major histocompatibility complex (MHC) class I-restricted antigen presentation. Interferon gamma treatment increases expression of MHC-encoded LMP2 and LMP7 subunits of the proteasome and decreases expression of two proteasome subunits, named X and Y, which alters the proteolytic specificity of proteasomes. Molecular cloning of complementary DNAs encoding X and Y showed that their proteins are proteasomal subunits with high amino acid similarity to LMP7 and LMP2, respectively. Thus, interferon gamma may induce subunit replacements of X and Y by LMP7 and LMP2, respectively, producing proteasomes perhaps more appropriate for the immunological processing of endogenous antigens.
引用
收藏
页码:1231 / 1234
页数:4
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