Abstract:
:Systematic screens for human disease genes have emerged in recent years, due to the wealth of information provided by genome sequences and large scale datasets. Here we review how integration of genomic data in yeast and human is helping to elucidate the genetic basis of mitochondrial diseases. The identification of nearly all yeast mitochondrial proteins and many of their functional interactions provides insight into the role of mitochondria in cellular processes. This information enables prioritization of the candidate genes underlying mitochondrial disorders. In an iterative fashion, the link between predicted human candidate genes and their disease phenotypes can be experimentally tested back in yeast.
journal_name
Mol Biosystjournal_title
Molecular bioSystemsauthors
Perocchi F,Mancera E,Steinmetz LMdoi
10.1039/b709494asubject
Has Abstractpub_date
2008-01-01 00:00:00pages
18-29issue
1eissn
1742-206Xissn
1742-2051journal_volume
4pub_type
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