Localisation of 26S proteasomes with different subunit composition in insect muscles undergoing programmed cell death

被引:16
作者
Löw, P
Hastings, RA
Dawson, SP
Sass, M
Billett, MA
Mayer, RJ
Reynolds, SE
机构
[1] Eotvos Lorand Univ, Dept Gen Zool, H-1445 Budapest, Hungary
[2] Univ Nottingham, Sch Biomed Sci, Nottingham NG7 2RD, England
[3] Univ Bath, Sch Biol & Biochem, Bath BA2 7AY, Avon, England
基金
匈牙利科学研究基金会; 英国惠康基金;
关键词
programmed cell death; tobacco hornworm; Manduca sexta; proteasome regulatory ATPase subunit; muscle degradation; immunogold method;
D O I
10.1038/sj.cdd.4400743
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 26S proteasome is a large multisubunit complex involved in degrading both cytoplasmic and nuclear proteins. We have investigated the subcellular distribution of four regulatory ATPase subunits (S6 (TBP7/MS73), S6' (TBP1), S7 (MSS1), and S10b (SUG2)) together with components of 20S proteasomes in the intersegmental muscles (ISM) of Manduca sexta during developmentally programmed cell death (PCD). Immunogold electron microscopy shows that S6 is located in the heterochromatic part of nuclei of ISM fibres. S6' is present in degraded material only outside intact fibres. S7 can be detected in nuclei, cytoplasm and also in degraded material, S10b, on the other hand, is initially found in nuclei and subsequently in degraded cytoplasmic locations during PCD. 20S proteasomes are present in all areas where ATPase subunits are detected, consistent with the presence of intact 26S proteasomes. These results are discussed in terms of heterogeneity of 26S proteasomes, 26S proteasome disassembly and the possible role of ATPases in non-proteasome complexes in the process of PCD.
引用
收藏
页码:1210 / 1217
页数:8
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