Cd2+, Mn2+, Ni2+ and Se2+ toxicity to Saccharomyces cerevisiae lacking YPK9p the orthologue of human ATP13A2

被引:105
作者
Schmidt, Karyn [1 ]
Wolfe, Devin M. [1 ]
Stiller, Barbara [4 ,5 ]
Pearce, David A. [1 ,2 ,3 ]
机构
[1] Univ Rochester, Sch Med & Dent, Ctr Neural Dev & Dis, Rochester, NY 14620 USA
[2] Univ Rochester, Sch Med & Dent, Dept Biochem & Biophys, Aab Inst Biomed Sci, Rochester, NY 14642 USA
[3] Univ Rochester, Sch Med & Dent, Dept Neurol, Rochester, NY 14642 USA
[4] Univ Cologne, Inst Human Genet, Cologne, Germany
[5] Univ Cologne, Inst Genet, D-5000 Cologne, Germany
关键词
ATP13A2; YPK9; Kufor-Rakeb syndrome; Parkinsonism; SUPEROXIDE-DISMUTASE; SELENIUM; PARKINSONISM; DISEASE; CELLS; TRANSFORMATION; LOCALIZATION; PEROXIDASE; INHIBITION; MUTATIONS;
D O I
10.1016/j.bbrc.2009.03.151
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 Saccharomyces cerevisiae gene YPK9 encodes a putative integral membrane protein which is 58% similar and 38% identical in amino acid sequence to the human lysosomal P-5B ATPase ATP13A2. Mutations in ATP13A2 have been found in patients with Kufor-Rakeb syndrome, a form of juvenile Parkinsonism. We report that Ypk9p localizes to the yeast vacuole and that deletion of YPK9 confers sensitivity for growth for cadmium, manganese, nickel or selenium. These results suggest that Ypk9p may play a role in sequestration of divalent heavy metal ions. Further studies on the function of Ypk9p/ATP13A2 may help to define the molecular basis of Kufor-Rakeb syndrome and provide a potential link to environmental factors such as heavy metals contributing to some forms of Parkinsonism. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:198 / 202
页数:5
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