DEVELOPMENTAL-CHANGES OF THE 26-S-PROTEASOME IN ABDOMINAL INTERSEGMENTAL MUSCLES OF MANDUCA-SEXTA DURING PROGRAMMED CELL-DEATH

被引:127
作者
DAWSON, SP
ARNOLD, JE
MAYER, NJ
REYNOLDS, SE
BILLETT, MA
GORDON, C
COLLEAUX, L
KLOETZEL, PM
TANAKA, K
MAYER, RJ
机构
[1] UNIV NOTTINGHAM,QUEENS MED CTR,SCH MED,DEPT BIOCHEM,NOTTINGHAM NG7 2UH,ENGLAND
[2] UNIV BATH,DEPT BIOCHEM & BIOL SCI,BATH BA2 7AY,AVON,ENGLAND
[3] HUMBOLDT UNIV BERLIN,FAC MED CHARITE,INST BIOCHEM,D-10115 BERLIN,GERMANY
[4] UNIV TOKUSHIMA,INST ENZYME RES,TOKUSHIMA 770,JAPAN
[5] WESTERN GEN HOSP,MRC,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
基金
英国惠康基金;
关键词
D O I
10.1074/jbc.270.4.1850
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
cDNA clone MS73 codes for an ATPase that is a regulatory subunit of the 26 S proteasome, Reverse transcriptase polymerase chain reaction analysis demonstrates that the expression of the gene dramatically increases in the pre-eclosion period, Western analyses show increases in other related ATPases including MS73, MSS1, and mts2 but not TBP1. A similar increase in the 30-kDa subunit of the 20 S proteasome occurs. There are accompanying large changes in the peptidase activities of the 26 S proteasome. Relative to the 30-kDa subunit, there is no change in MSS1 and MS73, a 3-fold increase in mts2, and a B-fold decline in TBP1. A large increase in the concentration of 26 S proteasomes together with extensive regulatory reprogramming may facilitate rapid muscular proteolysis.
引用
收藏
页码:1850 / 1858
页数:9
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