Genetics leaves no bones unturned

In their article, Gill and colleagues report their use of molecular genetic techniques to confirm that a group of human remains uncovered in Russia in 1991 include those of the last Tsar his wife and three of their children. The methodology for family lineage identification is based on the fact that...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature genetics 1994-02, Vol.6 (2), p.113-114
1. Verfasser: Debenham, Paul G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 114
container_issue 2
container_start_page 113
container_title Nature genetics
container_volume 6
creator Debenham, Paul G.
description In their article, Gill and colleagues report their use of molecular genetic techniques to confirm that a group of human remains uncovered in Russia in 1991 include those of the last Tsar his wife and three of their children. The methodology for family lineage identification is based on the fact that mitochondria are maternally derived and their genome contains highly variable segments suitable for DNA sequence analysis. As many copies of the mitochondrial genome exist within human cells the probability of finding intact copies in historic tissue is greatly improved. The family relationship is established by the examination of the inheritance of short tandem repeat (STR) sequences in the human genome. STR sequences, also known as microsatellites, are intermediately variable loci scattered richly throughout mammalian genomes, and contain a short nucleotide sequence ( similar to 2-5 nucleotides long) which is randomly repeated to a limited extent, say between 5 and 20 times. The short DNA sequences containing an STR is ideal for gene amplification analysis with each different repeat type (allele) distinguished by one repeat length difference using the latest gene analysis equipment.
doi_str_mv 10.1038/ng0294-113
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76443969</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76443969</sourcerecordid><originalsourceid>FETCH-LOGICAL-c349t-36019b7e1f8455c965d0199717ad59451f67075f71c2b40fc8380144585a82dd3</originalsourceid><addsrcrecordid>eNqFkE1Lw0AQhhdRaq1evAv14kGJ7mS_j1K0CgUvel6SzaSkpJu6mwj-e7ekeBI8zTDvw8vwEHIJ9B4o0w9-TXPDMwB2RKYguMxAgT5OO5WQccrkKTmLcUMpcE71hEw0yJzKfEqul-ixb1yct1h8YZz7bl52Pi2D74fgsTonJ3XRRrw4zBn5eH56X7xkq7fl6-JxlTnGTZ8xScGUCqHWXAhnpKjSwShQRSUMF1BLRZWoFbi85LR2mun9O0KLQudVxWbkZuzdhe5zwNjbbRMdtm3hsRuiVZJzZqT5FwRpQDCuE3g7gi50MQas7S402yJ8W6B2L86O4mwSl-CrQ-tQbrH6RQ-mUn435jElfo3BbrrkJxn5q-0HhchzBg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16915348</pqid></control><display><type>article</type><title>Genetics leaves no bones unturned</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><source>Nature Journals Online</source><creator>Debenham, Paul G.</creator><creatorcontrib>Debenham, Paul G.</creatorcontrib><description>In their article, Gill and colleagues report their use of molecular genetic techniques to confirm that a group of human remains uncovered in Russia in 1991 include those of the last Tsar his wife and three of their children. The methodology for family lineage identification is based on the fact that mitochondria are maternally derived and their genome contains highly variable segments suitable for DNA sequence analysis. As many copies of the mitochondrial genome exist within human cells the probability of finding intact copies in historic tissue is greatly improved. The family relationship is established by the examination of the inheritance of short tandem repeat (STR) sequences in the human genome. STR sequences, also known as microsatellites, are intermediately variable loci scattered richly throughout mammalian genomes, and contain a short nucleotide sequence ( similar to 2-5 nucleotides long) which is randomly repeated to a limited extent, say between 5 and 20 times. The short DNA sequences containing an STR is ideal for gene amplification analysis with each different repeat type (allele) distinguished by one repeat length difference using the latest gene analysis equipment.</description><identifier>ISSN: 1061-4036</identifier><identifier>EISSN: 1546-1718</identifier><identifier>DOI: 10.1038/ng0294-113</identifier><identifier>PMID: 8162062</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Agriculture ; Animal Genetics and Genomics ; Biomedical and Life Sciences ; Biomedicine ; bone ; Cancer Research ; DNA ; DNA Fingerprinting ; Family ; Gene Function ; Genome, Human ; genomes ; Human Genetics ; Humans ; inheritance ; man ; news-and-views ; repeated sequence ; Repetitive Sequences, Nucleic Acid ; short tandem repeat</subject><ispartof>Nature genetics, 1994-02, Vol.6 (2), p.113-114</ispartof><rights>Springer Nature America, Inc. 1994</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-36019b7e1f8455c965d0199717ad59451f67075f71c2b40fc8380144585a82dd3</citedby><cites>FETCH-LOGICAL-c349t-36019b7e1f8455c965d0199717ad59451f67075f71c2b40fc8380144585a82dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/ng0294-113$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/ng0294-113$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8162062$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Debenham, Paul G.</creatorcontrib><title>Genetics leaves no bones unturned</title><title>Nature genetics</title><addtitle>Nat Genet</addtitle><addtitle>Nat Genet</addtitle><description>In their article, Gill and colleagues report their use of molecular genetic techniques to confirm that a group of human remains uncovered in Russia in 1991 include those of the last Tsar his wife and three of their children. The methodology for family lineage identification is based on the fact that mitochondria are maternally derived and their genome contains highly variable segments suitable for DNA sequence analysis. As many copies of the mitochondrial genome exist within human cells the probability of finding intact copies in historic tissue is greatly improved. The family relationship is established by the examination of the inheritance of short tandem repeat (STR) sequences in the human genome. STR sequences, also known as microsatellites, are intermediately variable loci scattered richly throughout mammalian genomes, and contain a short nucleotide sequence ( similar to 2-5 nucleotides long) which is randomly repeated to a limited extent, say between 5 and 20 times. The short DNA sequences containing an STR is ideal for gene amplification analysis with each different repeat type (allele) distinguished by one repeat length difference using the latest gene analysis equipment.</description><subject>Agriculture</subject><subject>Animal Genetics and Genomics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>bone</subject><subject>Cancer Research</subject><subject>DNA</subject><subject>DNA Fingerprinting</subject><subject>Family</subject><subject>Gene Function</subject><subject>Genome, Human</subject><subject>genomes</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>inheritance</subject><subject>man</subject><subject>news-and-views</subject><subject>repeated sequence</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>short tandem repeat</subject><issn>1061-4036</issn><issn>1546-1718</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1Lw0AQhhdRaq1evAv14kGJ7mS_j1K0CgUvel6SzaSkpJu6mwj-e7ekeBI8zTDvw8vwEHIJ9B4o0w9-TXPDMwB2RKYguMxAgT5OO5WQccrkKTmLcUMpcE71hEw0yJzKfEqul-ixb1yct1h8YZz7bl52Pi2D74fgsTonJ3XRRrw4zBn5eH56X7xkq7fl6-JxlTnGTZ8xScGUCqHWXAhnpKjSwShQRSUMF1BLRZWoFbi85LR2mun9O0KLQudVxWbkZuzdhe5zwNjbbRMdtm3hsRuiVZJzZqT5FwRpQDCuE3g7gi50MQas7S402yJ8W6B2L86O4mwSl-CrQ-tQbrH6RQ-mUn435jElfo3BbrrkJxn5q-0HhchzBg</recordid><startdate>19940201</startdate><enddate>19940201</enddate><creator>Debenham, Paul G.</creator><general>Nature Publishing Group US</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>7T3</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19940201</creationdate><title>Genetics leaves no bones unturned</title><author>Debenham, Paul G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-36019b7e1f8455c965d0199717ad59451f67075f71c2b40fc8380144585a82dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Agriculture</topic><topic>Animal Genetics and Genomics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>bone</topic><topic>Cancer Research</topic><topic>DNA</topic><topic>DNA Fingerprinting</topic><topic>Family</topic><topic>Gene Function</topic><topic>Genome, Human</topic><topic>genomes</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>inheritance</topic><topic>man</topic><topic>news-and-views</topic><topic>repeated sequence</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>short tandem repeat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Debenham, Paul G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Human Genome Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Debenham, Paul G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetics leaves no bones unturned</atitle><jtitle>Nature genetics</jtitle><stitle>Nat Genet</stitle><addtitle>Nat Genet</addtitle><date>1994-02-01</date><risdate>1994</risdate><volume>6</volume><issue>2</issue><spage>113</spage><epage>114</epage><pages>113-114</pages><issn>1061-4036</issn><eissn>1546-1718</eissn><abstract>In their article, Gill and colleagues report their use of molecular genetic techniques to confirm that a group of human remains uncovered in Russia in 1991 include those of the last Tsar his wife and three of their children. The methodology for family lineage identification is based on the fact that mitochondria are maternally derived and their genome contains highly variable segments suitable for DNA sequence analysis. As many copies of the mitochondrial genome exist within human cells the probability of finding intact copies in historic tissue is greatly improved. The family relationship is established by the examination of the inheritance of short tandem repeat (STR) sequences in the human genome. STR sequences, also known as microsatellites, are intermediately variable loci scattered richly throughout mammalian genomes, and contain a short nucleotide sequence ( similar to 2-5 nucleotides long) which is randomly repeated to a limited extent, say between 5 and 20 times. The short DNA sequences containing an STR is ideal for gene amplification analysis with each different repeat type (allele) distinguished by one repeat length difference using the latest gene analysis equipment.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>8162062</pmid><doi>10.1038/ng0294-113</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1061-4036
ispartof Nature genetics, 1994-02, Vol.6 (2), p.113-114
issn 1061-4036
1546-1718
language eng
recordid cdi_proquest_miscellaneous_76443969
source MEDLINE; Springer Nature - Complete Springer Journals; Nature Journals Online
subjects Agriculture
Animal Genetics and Genomics
Biomedical and Life Sciences
Biomedicine
bone
Cancer Research
DNA
DNA Fingerprinting
Family
Gene Function
Genome, Human
genomes
Human Genetics
Humans
inheritance
man
news-and-views
repeated sequence
Repetitive Sequences, Nucleic Acid
short tandem repeat
title Genetics leaves no bones unturned
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T16%3A43%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetics%20leaves%20no%20bones%20unturned&rft.jtitle=Nature%20genetics&rft.au=Debenham,%20Paul%20G.&rft.date=1994-02-01&rft.volume=6&rft.issue=2&rft.spage=113&rft.epage=114&rft.pages=113-114&rft.issn=1061-4036&rft.eissn=1546-1718&rft_id=info:doi/10.1038/ng0294-113&rft_dat=%3Cproquest_cross%3E76443969%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16915348&rft_id=info:pmid/8162062&rfr_iscdi=true