HOMOLOGY OF PROTEASOME SUBUNITS TO A MAJOR HISTOCOMPATIBILITY COMPLEX-LINKED LMP GENE

被引:255
作者
MARTINEZ, CK [1 ]
MONACO, JJ [1 ]
机构
[1] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT PATHOL,RICHMOND,VA 23298
关键词
D O I
10.1038/353664a0
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
THE ClaSS II region of the major histocompatibility complex (MHC) contains genes encoding at least two subunits of a large, intracellular protein complex (the low molecular mass polypeptide, or LMP, complex) 1-3. This complex is biochemically similar to the proteasome, an abundant and well conserved protein complex having multiple proteolytic activities. Here we report the isolation of a complementary DNA corresponding to one of the subunits of the LMP complex, LMP-2. The protein predicted from this cDNA sequence closely matches the amino-terminal peptide sequence of a rat proteasome subunit, confirming that the proteasome and the LMP complex share polypeptide subunits. The LMP-2 gene is tightly linked to HAM1, a gene thought to be required for translocating peptide fragments of endogenous antigens into the endoplasmic reticulum for association with MHC class I molecules 4. These observations suggest that the LMP complex may be responsible for generating peptides from cytoplasmic antigen during antigen processing.
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页码:664 / 667
页数:4
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