Evolution of DNA in heterochromatin: the Drosophila melanogaster sibling species subgroup as a resource
The Drosophila melanogaster species subgroup is a closely-knit collection of eight sibling species whose relationships are well defined. These species are too close for most evolutionary studies of euchromatic genes but are ideal to investigate the major changes that occur to DNA in heterochromatin...
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Veröffentlicht in: | Genetica 2000-07, Vol.109 (1-2), p.125-130 |
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description | The Drosophila melanogaster species subgroup is a closely-knit collection of eight sibling species whose relationships are well defined. These species are too close for most evolutionary studies of euchromatic genes but are ideal to investigate the major changes that occur to DNA in heterochromatin over short periods during evolution. For example, it is not known whether the locations of genes in heterochromatin are conserved over this time. The 18S and 28S ribosomal RNA genes can be considered as genuine heterochromatic genes. In D. melanogaster the rRNA genes are located at two sites, one each on the X and Y chromosome. In the other seven sibling species, rRNA genes are also located on the sex chromosomes but the positions often vary significantly, particularly on the Y. Furthermore, rDNA has been lost from the Y chromosome of both D. simulans and D. sechellia, presumably after separation of the line leading to present-day D. mauritiana. We conclude that changes to chromosomal position and copy number of rDNA arrays occur over much shorter evolutionary timespans than previously thought. In these respects the rDNA behaves more like the tandemly repeated satellite DNAs than euchromatic genes. |
doi_str_mv | 10.1023/A:1026588217432 |
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In these respects the rDNA behaves more like the tandemly repeated satellite DNAs than euchromatic genes.</description><identifier>ISSN: 0016-6707</identifier><identifier>EISSN: 1573-6857</identifier><identifier>DOI: 10.1023/A:1026588217432</identifier><identifier>PMID: 11293787</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Animals ; Biological evolution ; Chromosomes ; Copy number ; Deoxyribonucleic acid ; DNA ; Drosophila ; Drosophila mauritiana ; Drosophila melanogaster ; Drosophila melanogaster - genetics ; Drosophila sechellia ; Drosophila simulans ; Evolution, Molecular ; Evolutionary genetics ; Fruit flies ; Genes ; Genetics ; Heterochromatin ; Heterochromatin - genetics ; Insects ; RNA, Ribosomal - genetics ; rRNA 18S ; rRNA 28S ; Sex chromosomes ; Sibling species ; Species Specificity ; Subgroups ; Y chromosomes</subject><ispartof>Genetica, 2000-07, Vol.109 (1-2), p.125-130</ispartof><rights>Kluwer Academic Publishers 2000.</rights><rights>Kluwer Academic Publishers 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-87371e4171147a15ee48913b0549ecd86282962803e7ca613c057a068fb170a23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11293787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lohe, A R</creatorcontrib><creatorcontrib>Roberts, P A</creatorcontrib><title>Evolution of DNA in heterochromatin: the Drosophila melanogaster sibling species subgroup as a resource</title><title>Genetica</title><addtitle>Genetica</addtitle><description>The Drosophila melanogaster species subgroup is a closely-knit collection of eight sibling species whose relationships are well defined. These species are too close for most evolutionary studies of euchromatic genes but are ideal to investigate the major changes that occur to DNA in heterochromatin over short periods during evolution. For example, it is not known whether the locations of genes in heterochromatin are conserved over this time. The 18S and 28S ribosomal RNA genes can be considered as genuine heterochromatic genes. In D. melanogaster the rRNA genes are located at two sites, one each on the X and Y chromosome. In the other seven sibling species, rRNA genes are also located on the sex chromosomes but the positions often vary significantly, particularly on the Y. Furthermore, rDNA has been lost from the Y chromosome of both D. simulans and D. sechellia, presumably after separation of the line leading to present-day D. mauritiana. We conclude that changes to chromosomal position and copy number of rDNA arrays occur over much shorter evolutionary timespans than previously thought. In these respects the rDNA behaves more like the tandemly repeated satellite DNAs than euchromatic genes.</description><subject>Animals</subject><subject>Biological evolution</subject><subject>Chromosomes</subject><subject>Copy number</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Drosophila</subject><subject>Drosophila mauritiana</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila sechellia</subject><subject>Drosophila simulans</subject><subject>Evolution, Molecular</subject><subject>Evolutionary genetics</subject><subject>Fruit flies</subject><subject>Genes</subject><subject>Genetics</subject><subject>Heterochromatin</subject><subject>Heterochromatin - genetics</subject><subject>Insects</subject><subject>RNA, Ribosomal - genetics</subject><subject>rRNA 18S</subject><subject>rRNA 28S</subject><subject>Sex chromosomes</subject><subject>Sibling species</subject><subject>Species Specificity</subject><subject>Subgroups</subject><subject>Y chromosomes</subject><issn>0016-6707</issn><issn>1573-6857</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0U1r3DAQBmBRWpJtmnNvQbTQnJxqJEsj57bkG5b2kpyN7MzuKtiWI9mB_vtqSXopJDmMRoeHlxmGsa8gTkBI9XN5mpvR1krAUskPbAEaVWGsxo9sIQSYwqDAffY5pQchRIWm2mP7ALJSaHHBNhdPoZsnHwYe1vz815L7gW9pohjabQy9m_xwyqct8fMYUhi3vnO8p84NYeNSZjz5pvPDhqeRWk-Jp7nZxDCP3CXueKQU5tjSF_Zp7bpEhy_9gN1dXtyeXRer31c3Z8tV0ZaAU2FRIVD-ApToQBOVtgLVCF1W1N5bI62s8iMUYesMqFZodMLYdQMonFQH7Pg5d4zhcaY01b1PLXV5YApzqq1WJRqUmOWPNyVKbRXkeg8CYmZVmeG3_-BD3n3I69ZotLBWyF3a99eQNEbZPBnuoo5e1Nz0dF-P0fcu_qn_HU79BXZel5E</recordid><startdate>20000701</startdate><enddate>20000701</enddate><creator>Lohe, A R</creator><creator>Roberts, P A</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>20000701</creationdate><title>Evolution of DNA in heterochromatin: the Drosophila melanogaster sibling species subgroup as a resource</title><author>Lohe, A R ; 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These species are too close for most evolutionary studies of euchromatic genes but are ideal to investigate the major changes that occur to DNA in heterochromatin over short periods during evolution. For example, it is not known whether the locations of genes in heterochromatin are conserved over this time. The 18S and 28S ribosomal RNA genes can be considered as genuine heterochromatic genes. In D. melanogaster the rRNA genes are located at two sites, one each on the X and Y chromosome. In the other seven sibling species, rRNA genes are also located on the sex chromosomes but the positions often vary significantly, particularly on the Y. Furthermore, rDNA has been lost from the Y chromosome of both D. simulans and D. sechellia, presumably after separation of the line leading to present-day D. mauritiana. We conclude that changes to chromosomal position and copy number of rDNA arrays occur over much shorter evolutionary timespans than previously thought. In these respects the rDNA behaves more like the tandemly repeated satellite DNAs than euchromatic genes.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>11293787</pmid><doi>10.1023/A:1026588217432</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Biological evolution Chromosomes Copy number Deoxyribonucleic acid DNA Drosophila Drosophila mauritiana Drosophila melanogaster Drosophila melanogaster - genetics Drosophila sechellia Drosophila simulans Evolution, Molecular Evolutionary genetics Fruit flies Genes Genetics Heterochromatin Heterochromatin - genetics Insects RNA, Ribosomal - genetics rRNA 18S rRNA 28S Sex chromosomes Sibling species Species Specificity Subgroups Y chromosomes |
title | Evolution of DNA in heterochromatin: the Drosophila melanogaster sibling species subgroup as a resource |
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