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dfh is a Drosophila homolog of the Friedreich's ataxia disease gene
A putative Drosophila homolog of the Friedreich's ataxia disease gene ( FRDA) has been cloned and characterized; it has been named Drosophila frataxin homolog ( dfh). It is located at 8C/D position on X chromosome and is spread over 1 kb, a much smaller genomic region than the human gene. Its g...
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Published in: | Gene 2000-10, Vol.256 (1), p.35-42 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A putative
Drosophila homolog of the Friedreich's ataxia disease gene (
FRDA) has been cloned and characterized; it has been named
Drosophila frataxin homolog (
dfh). It is located at 8C/D position on X chromosome and is spread over 1
kb, a much smaller genomic region than the human gene. Its genomic organization is simple, with a single intron dividing the coding region into two exons. The predicted encoded product has 190 amino acids, being considered a frataxin-like protein on the basis of the sequence and secondary structure conservation when compared with human frataxin and related proteins from other eukaryotes. The closest match between the
Drosophila and the human proteins involved a stretch of 38 amino acids at C-terminus, encoded by
dfh exon 2, and exons 4 and 5a of the
FRDA gene, respectively. This highly conserved region is very likely to form a functional domain with a β sheet structure flanked by α-helices where the sequence is less conserved. A signal peptide for mitochondrial import has also been predicted in the
Drosophila frataxin-like protein, suggesting its mitochondrial localization, as occurs for human frataxin and other frataxin-like proteins described in eukaryotes. The
Drosophila gene is expressed throughout the development of this organism, with a peak of expression in 6–12
h embryos, and showing a spatial ubiquitous pattern from 4
h embryos to the last embryonic stage examined. The isolation of
dfh will soon make available specific
dfh mutants that help in understanding the pathogenesis of FRDA. |
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ISSN: | 0378-1119 1879-0038 |
DOI: | 10.1016/S0378-1119(00)00343-7 |