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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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description | 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. |
doi_str_mv | 10.1016/S0378-1119(00)00343-7 |
format | article |
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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.</description><identifier>ISSN: 0378-1119</identifier><identifier>EISSN: 1879-0038</identifier><identifier>DOI: 10.1016/S0378-1119(00)00343-7</identifier><identifier>PMID: 11054533</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Animals ; Blotting, Northern ; Cloning, Molecular ; dfh gene ; DNA - chemistry ; DNA - genetics ; DNA, Complementary - chemistry ; DNA, Complementary - genetics ; Drosophila ; Drosophila - genetics ; Drosophila melanogaster - genetics ; Drosophila Proteins ; Embryo, Nonmammalian - metabolism ; Embryonic Development ; Exons ; Frataxin ; Frataxin-like proteins ; FRDA gene ; Friedreich Ataxia - genetics ; Friedreich's ataxia ; Gene Expression Regulation, Developmental ; Genes, Insect - genetics ; In Situ Hybridization ; Introns ; Iron-Binding Proteins ; Model organism ; Molecular Sequence Data ; Phosphotransferases (Alcohol Group Acceptor) - genetics ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Sequence Alignment ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid</subject><ispartof>Gene, 2000-10, Vol.256 (1), p.35-42</ispartof><rights>2000 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-7b86f45af82ebffa4903cf299ee26d6d0db82b928c3c9307e0c8a2007cc0a4973</citedby><cites>FETCH-LOGICAL-c392t-7b86f45af82ebffa4903cf299ee26d6d0db82b928c3c9307e0c8a2007cc0a4973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11054533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cañizares, Joaquı́n</creatorcontrib><creatorcontrib>Blanca, José M</creatorcontrib><creatorcontrib>Navarro, Juan A</creatorcontrib><creatorcontrib>Monrós, Eugenia</creatorcontrib><creatorcontrib>Palau, Francisco</creatorcontrib><creatorcontrib>Moltó, Marı́a D</creatorcontrib><title>dfh is a Drosophila homolog of the Friedreich's ataxia disease gene</title><title>Gene</title><addtitle>Gene</addtitle><description>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.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Blotting, Northern</subject><subject>Cloning, Molecular</subject><subject>dfh gene</subject><subject>DNA - chemistry</subject><subject>DNA - genetics</subject><subject>DNA, Complementary - chemistry</subject><subject>DNA, Complementary - genetics</subject><subject>Drosophila</subject><subject>Drosophila - genetics</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila Proteins</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Embryonic Development</subject><subject>Exons</subject><subject>Frataxin</subject><subject>Frataxin-like proteins</subject><subject>FRDA gene</subject><subject>Friedreich Ataxia - genetics</subject><subject>Friedreich's ataxia</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genes, Insect - genetics</subject><subject>In Situ Hybridization</subject><subject>Introns</subject><subject>Iron-Binding Proteins</subject><subject>Model organism</subject><subject>Molecular Sequence Data</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - genetics</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology, Amino Acid</subject><issn>0378-1119</issn><issn>1879-0038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkMlOwzAQQC0EgrJ8AsgnlkNgbCdxckKoUEBC4gCcLcceE6O0LnaK4O9JaQVH5jIa6c32CDlkcM6AlRdPIGSVMcbqU4AzAJGLTG6QEatknQ1ltUlGv8gO2U3pDYYoCr5NdhiDIi-EGJGxdS31iWp6HUMK89Z3mrZhGrrwSoOjfYt0Ej3aiN60JwPY60-vqfUJdUL6ijPcJ1tOdwkP1nmPvExunsd32cPj7f346iEzouZ9JpuqdHmhXcWxcU7nNQjjeF0j8tKWFmxT8abmlRGmFiARTKU5gDQGBliKPXK8mjuP4X2BqVdTnwx2nZ5hWCQluShlIYp_QSal4DlfgsUKNMPzKaJT8-inOn4pBmqpWf1oVkuHCkD9aFbLS47WCxbNFO1f19rrAFyuABx8fHiMKhmPM4PWRzS9ssH_s-Ibz3-LLQ</recordid><startdate>20001003</startdate><enddate>20001003</enddate><creator>Cañizares, Joaquı́n</creator><creator>Blanca, José M</creator><creator>Navarro, Juan A</creator><creator>Monrós, Eugenia</creator><creator>Palau, Francisco</creator><creator>Moltó, Marı́a D</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20001003</creationdate><title>dfh is a Drosophila homolog of the Friedreich's ataxia disease gene</title><author>Cañizares, Joaquı́n ; Blanca, José M ; Navarro, Juan A ; Monrós, Eugenia ; Palau, Francisco ; Moltó, Marı́a D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-7b86f45af82ebffa4903cf299ee26d6d0db82b928c3c9307e0c8a2007cc0a4973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Blotting, Northern</topic><topic>Cloning, Molecular</topic><topic>dfh gene</topic><topic>DNA - chemistry</topic><topic>DNA - genetics</topic><topic>DNA, Complementary - chemistry</topic><topic>DNA, Complementary - genetics</topic><topic>Drosophila</topic><topic>Drosophila - genetics</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila Proteins</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Embryonic Development</topic><topic>Exons</topic><topic>Frataxin</topic><topic>Frataxin-like proteins</topic><topic>FRDA gene</topic><topic>Friedreich Ataxia - genetics</topic><topic>Friedreich's ataxia</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genes, Insect - genetics</topic><topic>In Situ Hybridization</topic><topic>Introns</topic><topic>Iron-Binding Proteins</topic><topic>Model organism</topic><topic>Molecular Sequence Data</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Sequence Alignment</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cañizares, Joaquı́n</creatorcontrib><creatorcontrib>Blanca, José M</creatorcontrib><creatorcontrib>Navarro, Juan A</creatorcontrib><creatorcontrib>Monrós, Eugenia</creatorcontrib><creatorcontrib>Palau, Francisco</creatorcontrib><creatorcontrib>Moltó, Marı́a D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Gene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cañizares, Joaquı́n</au><au>Blanca, José M</au><au>Navarro, Juan A</au><au>Monrós, Eugenia</au><au>Palau, Francisco</au><au>Moltó, Marı́a D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>dfh is a Drosophila homolog of the Friedreich's ataxia disease gene</atitle><jtitle>Gene</jtitle><addtitle>Gene</addtitle><date>2000-10-03</date><risdate>2000</risdate><volume>256</volume><issue>1</issue><spage>35</spage><epage>42</epage><pages>35-42</pages><issn>0378-1119</issn><eissn>1879-0038</eissn><abstract>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.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>11054533</pmid><doi>10.1016/S0378-1119(00)00343-7</doi><tpages>8</tpages></addata></record> |
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source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Amino Acid Sequence Animals Blotting, Northern Cloning, Molecular dfh gene DNA - chemistry DNA - genetics DNA, Complementary - chemistry DNA, Complementary - genetics Drosophila Drosophila - genetics Drosophila melanogaster - genetics Drosophila Proteins Embryo, Nonmammalian - metabolism Embryonic Development Exons Frataxin Frataxin-like proteins FRDA gene Friedreich Ataxia - genetics Friedreich's ataxia Gene Expression Regulation, Developmental Genes, Insect - genetics In Situ Hybridization Introns Iron-Binding Proteins Model organism Molecular Sequence Data Phosphotransferases (Alcohol Group Acceptor) - genetics RNA, Messenger - genetics RNA, Messenger - metabolism Sequence Alignment Sequence Analysis, DNA Sequence Homology, Amino Acid |
title | dfh is a Drosophila homolog of the Friedreich's ataxia disease gene |
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