Proteasomes and proteasome activator 200 kDa (PA200) accumulate on chromatin in response to ionizing radiation

被引:41
作者
Blickwedehl, Jennifer
McEvoy, Sarah
Wong, Irene
Kousis, Philaretos
Clements, James
Elliott, Rosemary
Cresswell, Peter
Liang, Ping
Bangia, Naveen
机构
[1] Roswell Pk Canc Inst, Dept Immunol, Buffalo, NY 14263 USA
[2] Roswell Pk Canc Inst, Dept Mol & Cellular Biol, Buffalo, NY 14263 USA
[3] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, Immunobiol Sect, New Haven, CT 06510 USA
关键词
D O I
10.1667/RR0690.1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proteasome activator 200 kDa (PA200) forms nuclear foci after exposure of cells to ionizing radiation and enhances proteasome activity in vitro. Within cells, it is unclear whether PA200 responds to radiation alone or in association with proteasomes. In the present study, we identified three forms of cellular PA200 (termed PA200i, ii and iii) at the mRNA and protein levels. Neither PA200ii nor PA200iii appears to associate with proteasomes. All detectable PA200i is associated with proteasomes, which indicates that PA200i and proteasomes function together within the cell. Consistent with this idea, we find that exposure of cells to radiation leads to an equivalent accumulation of both PA200i and core proteasomes on chromatin. This increase in PA200 and proteasomes on chromatin is not specific to the stage of cell cycle arrest since it occurs in cells that arrest in G(2)/M and cells that arrest in G(1)/S after exposure to radiation. These data provide evidence that PA200 and proteasomes function together within cells and respond to a specific radiation-induced damage independent of the stage of cell cycle arrest. (C) 2007 by Radiation Research Society
引用
收藏
页码:663 / 674
页数:12
相关论文
共 46 条
[1]  
Bangia N, 1999, EUR J IMMUNOL, V29, P1858, DOI 10.1002/(SICI)1521-4141(199906)29:06<1858::AID-IMMU1858>3.0.CO
[2]  
2-C
[3]   Structure and functions of the 20S and 26S proteasomes [J].
Coux, O ;
Tanaka, K ;
Goldberg, AL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :801-847
[4]   HOMOZYGOUS DELETIONS THAT SIMULTANEOUSLY ELIMINATE EXPRESSIONS OF CLASS-I AND CLASS-II ANTIGENS OF EBV-TRANSFORMED B-LYMPHOBLASTOID CELLS .1. REDUCED PROLIFERATIVE RESPONSES OF AUTOLOGOUS AND ALLOGENEIC T-CELLS TO MUTANT-CELLS THAT HAVE DECREASED EXPRESSION OF CLASS-II ANTIGENS [J].
DEMARS, R ;
CHANG, CC ;
SHAW, S ;
REITNAUER, PJ ;
SONDEL, PM .
HUMAN IMMUNOLOGY, 1984, 11 (02) :77-97
[5]   Disulfide bond isomerization and the assembly of MHC class I-Peptide complexes [J].
Dick, TP ;
Bangia, N ;
Peaper, DR ;
Cresswell, P .
IMMUNITY, 2002, 16 (01) :87-98
[6]   Coordinated dual cleavages induced by the proteasome regulator PA28 lead to dominant MHC ligands [J].
Dick, TP ;
Ruppert, T ;
Groettrup, M ;
Kloetzel, PM ;
Kuehn, L ;
Koszinowski, UH ;
Stevanovic, S ;
Schild, H ;
Rammensee, HG .
CELL, 1996, 86 (02) :253-262
[7]   A role for calnexin in the assembly of the MHC class I loading complex in the endoplasmic reticulum [J].
Diedrich, G ;
Bangia, N ;
Pan, M ;
Cresswell, P .
JOURNAL OF IMMUNOLOGY, 2001, 166 (03) :1703-1709
[8]   Hairless contains a novel nuclear matrix targeting signal and associates with histone deacetylase 3 in nuclear speckles [J].
Djabali, K ;
Christiano, AM .
DIFFERENTIATION, 2004, 72 (08) :410-418
[9]   MHC-LINKED LMP GENE-PRODUCTS SPECIFICALLY ALTER PEPTIDASE ACTIVITIES OF THE PROTEASOME [J].
DRISCOLL, J ;
BROWN, MG ;
FINLEY, D ;
MONACO, JJ .
NATURE, 1993, 365 (6443) :262-264
[10]  
DUBIEL W, 1992, J BIOL CHEM, V267, P22369