CLONING AND SEQUENCING A NON-ATPASE SUBUNIT OF THE REGULATORY COMPLEX OF THE DROSOPHILA 26S-PROTEASE

被引:34
作者
HARACSKA, L [1 ]
UDVARDY, A [1 ]
机构
[1] HUNGARIAN ACAD SCI, BIOL RES CTR, INST BIOCHEM, H-6701 SZEGED, HUNGARY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1995年 / 231卷 / 03期
关键词
26S PROTEASE; 20S PROTEOSOME; ADENOSINE-TRIPHOSPHATASE DOMAINS; UBIQUITIN; PROTEIN DEGRADATION;
D O I
10.1111/j.1432-1033.1995.0720d.x
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
We have cloned and sequenced a non-ATPase subunit of the regulatory complex of the Drosophila 26S protease. The gene is present in a single copy in the Drosophila genome. By comparing the nucleotide sequence of the genomic and cDNA clones three exons and two introns were localized. Two transcription start sites were identified 9 bp apart. The deduced protein sequence shows no significant similarity to any other protein in the database. In Drosophila embryos where the 26S protease is present in high concentration, the pool of free subunits of the regulatory complex is very low. Among the free subunits of the regulatory complex the cloned subunit is present in very large excess. This observation raises the possibility that this subunit is in a dynamic equilibrium, exchanging between a free and a particle-bound form, which may have important implications concerning its function.
引用
收藏
页码:720 / 725
页数:6
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