Trypanosomes contain two highly different isoforms of peroxin PEX13 involved in glycosome biogenesis

被引:20
作者
Brennand, Ana [1 ,2 ]
Rigden, Daniel J. [3 ]
Michels, Paul A. M. [1 ,2 ]
机构
[1] Catholic Univ Louvain, Trop Dis Res Unit, Duve Inst, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Biochem Lab, B-1200 Brussels, Belgium
[3] Univ Liverpool, Inst Integrat Biol, Liverpool L69 7ZB, Merseyside, England
关键词
Trypanosoma; Glycosome; Peroxisome; Biogenesis; Docking complex; Peroxin; PROTEIN DATABASE SEARCHES; INDUCIBLE EXPRESSION; MATRIX PROTEINS; PSI-BLAST; BRUCEI; COMPARTMENTATION; IDENTIFICATION; LOCALIZATION; IMPORT;
D O I
10.1016/j.febslet.2012.05.019
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 previously identified the peroxin PEX13 in Trypanosoma brucei. Although lacking some features considered typical of PEX13s, it appeared functional in the biogenesis of glycosomes, the peroxisome-like organelles of trypanosomatids. Here we report the identification of a very different trypanosomatid PEX13, not containing the commonly encountered PEX13 SH3 domain but having other typical features. It is readily detected with the jackhmmer database search program, but not with PSI-BLAST. This is the first time different PEX13 isoforms are reported in a single organism. We show that this PEX13.2, like the PEX13.1 previously described, is associated with glycosomes and that its depletion by RNA interference affects the biogenesis of the organelles and viability of trypanosomes. The features considered typical of PEX13s are discussed.
引用
收藏
页码:1765 / 1771
页数:7
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