Mitochondrial functional interactions between frataxin and Isu1p, the iron-sulfur cluster scaffold protein, in Saccharomyces cerevisiae

被引:103
|
作者
Ramazzotti, A [1 ]
Vanmansart, V [1 ]
Foury, F [1 ]
机构
[1] Unite Biochim Physiol, B-1348 Louvain, Belgium
关键词
Fe-S cluster; frataxin; ISU; synthetic lethal; yeast;
D O I
10.1016/S0014-5793(03)01498-4
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
Friedreich's ataxia is caused by a deficit in the mitochondrial protein frataxin. The present work demonstrates that in vivo yeast frataxin Yfh1p and Isu1p, the mitochondrial scaffold protein for the Fe-S cluster assembly, have tightly linked biological functions, acting in concert to promote the Fe-S cluster assembly. A synthetic lethal screen on high iron media with the mild G107D yfh1 mutant has specifically identified Isu1p. Analysis of the cellular phenotypes resulting from pairwise combinations of yfh1 and isu1 mutations, and crosslinking experiments in isolated mitochondria provide evidence for a direct interaction between Yfh1p and Isu1p. (C) 2003 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:215 / 220
页数:6
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