Immunoproteasome assembly:: Cooperative incorporation of interferon γ (IFN-γ)-inducible subunits

被引:358
作者
Griffin, TA
Nandi, D
Cruz, M
Fehling, HJ
Van Kaer, L
Monaco, JJ
Colbert, RA
机构
[1] Childrens Hosp, Med Ctr, William S Rowe Div Rheumatol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Sch Med, Howard Hughes Med Inst, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Sch Med, Dept Mol Genet, Cincinnati, OH 45267 USA
[4] Basel Inst Immunol, CH-4005 Basel, Switzerland
[5] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Sch Med, Howard Hughes Med Inst, Nashville, TN 37232 USA
关键词
D O I
10.1084/jem.187.1.97
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
LMP2, LMP7, and MECL are interferon gamma-inducible catalytic subunits of vertebrate 20S proteasomes, which can replace constitutive catalytic subunits (delta, X, and Z, respectively) during proteasome biogenesis. We demonstrate that MECL requires LMP2 for efficient incorporation into preproteasomes, and preproteasomes containing LMP2 and MECL require LMP7 for efficient maturation. The latter effect depends on the presequence of LMP7, but not on LMP7 catalytic activity. This cooperative mechanism favors the assembly of homogeneous "immuno-proteasomes" containing all three inducible subunits, suggesting that these subunits act in concert to enhance proteasomal generation of major histocompatibility complex class I-binding peptides.
引用
收藏
页码:97 / 104
页数:8
相关论文
共 34 条
[1]   CDNA CLONING AND INTERFERON-GAMMA DOWN-REGULATION OF PROTEASOMAL SUBUNIT-X AND SUBUNIT-Y [J].
AKIYAMA, KY ;
YOKOTA, KY ;
KAGAWA, S ;
SHIMBARA, N ;
TAMURA, T ;
AKIOKA, H ;
NOTHWANG, HG ;
NODA, C ;
TANAKA, K ;
ICHIHARA, A .
SCIENCE, 1994, 265 (5176) :1231-1234
[2]   INTERFERON-GAMMA STIMULATION MODULATES THE PROTEOLYTIC ACTIVITY AND CLEAVAGE SITE PREFERENCE OF 20S MOUSE PROTEASOMES [J].
BOES, B ;
HENGEL, H ;
RUPPERT, T ;
MULTHAUP, G ;
KOSZINOWSKI, UH ;
KLOETZEL, PM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :901-909
[3]   Autocatalytic subunit processing couples active site formation in the 20S proteasome to completion of assembly [J].
Chen, P ;
Hochstrasser, M .
CELL, 1996, 86 (06) :961-972
[4]   Structure and functions of the 20S and 26S proteasomes [J].
Coux, O ;
Tanaka, K ;
Goldberg, AL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :801-847
[5]   Effects of major-histocompatibility-complex-encoded subunits on the peptidase and proteolytic activities of human 20S proteasomes - Cleavage of proteins and antigenic peptides [J].
Ehring, B ;
Meyer, TH ;
Eckerskorn, C ;
Lottspeich, F ;
Tampe, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 235 (1-2) :404-415
[6]   MHC CLASS-I EXPRESSION IN MICE LACKING THE PROTEASOME SUBUNIT LMP-7 [J].
FEHLING, HJ ;
SWAT, W ;
LAPLACE, C ;
KUHN, R ;
RAJEWSKY, K ;
MULLER, U ;
VONBOEHMER, H .
SCIENCE, 1994, 265 (5176) :1234-1237
[7]   20-S PROTEASOMES ARE ASSEMBLED VIA DISTINCT PRECURSOR COMPLEXES - PROCESSING OF LMP2 AND LMP7 PROPROTEINS TAKES PLACE IN 13-16-S PREPROTEASOME COMPLEXES [J].
FRENTZEL, S ;
PESOLDHURT, B ;
SEELIG, A ;
KLOETZEL, PM .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 236 (04) :975-981
[8]  
FRUH K, 1992, J BIOL CHEM, V267, P22131
[9]   PEPTIDASE ACTIVITIES OF PROTEASOMES ARE DIFFERENTIALLY REGULATED BY THE MAJOR HISTOCOMPATIBILITY COMPLEX-ENCODED GENES FOR LMP2 AND LMP7 [J].
GACZYNSKA, M ;
ROCK, KL ;
SPIES, T ;
GOLDBERG, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9213-9217
[10]   Proteasome subunits X and Y alter peptidase activities in opposite ways to the interferon-gamma-induced subunits LMP2 and LMP7 [J].
Gaczynska, M ;
Goldberg, AL ;
Tanaka, K ;
Hendil, KB ;
Rock, KL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (29) :17275-17280