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A Genomic Scanning Method for Higher Organisms Using Restriction Sites as Landmarks
We have developed a powerful genomic scanning method, termed "restriction landmark genomic scanning," that is useful for analysis of the genomic DNA of higher organisms using restriction sites as landmarks. Genomic DNA is radioactively labeled at cleavage sites specific for a rare cleaving...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1991-11, Vol.88 (21), p.9523-9527 |
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container_end_page | 9527 |
container_issue | 21 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Hatada, Izuho Hayashizaki, Yoshihide Hirotsune, Shinji Komatsubara, Hideyuki Mukai, Tsunehiro |
description | We have developed a powerful genomic scanning method, termed "restriction landmark genomic scanning," that is useful for analysis of the genomic DNA of higher organisms using restriction sites as landmarks. Genomic DNA is radioactively labeled at cleavage sites specific for a rare cleaving restriction enzyme and then size-fractionated in one dimension. The fractionated DNA is further digested with another more frequently occurring enzyme and separated in the second dimension. This procedure gives a two-dimensional pattern with thousands of scattered spots corresponding to sites for the first enzyme, indicating that the genome of mammals can be scanned at ≈1-megabase intervals. The position and intensity of a spot reflect its locus and the copy number of the corresponding restriction site, respectively, based on the nature of the end-labeling system. Therefore, this method is widely applicable to genome mapping or detection of alterations in a genome. |
doi_str_mv | 10.1073/pnas.88.21.9523 |
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Genomic DNA is radioactively labeled at cleavage sites specific for a rare cleaving restriction enzyme and then size-fractionated in one dimension. The fractionated DNA is further digested with another more frequently occurring enzyme and separated in the second dimension. This procedure gives a two-dimensional pattern with thousands of scattered spots corresponding to sites for the first enzyme, indicating that the genome of mammals can be scanned at ≈1-megabase intervals. The position and intensity of a spot reflect its locus and the copy number of the corresponding restriction site, respectively, based on the nature of the end-labeling system. Therefore, this method is widely applicable to genome mapping or detection of alterations in a genome.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.88.21.9523</identifier><identifier>PMID: 1946366</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Animals ; Biological and medical sciences ; Chromosome Mapping ; Cloning, Molecular ; DNA ; Drosophila ; Drosophila melanogaster - genetics ; Electrophoresis ; Electrophoresis, Gel, Two-Dimensional ; Enzymes ; Fractionation ; Fundamental and applied biological sciences. Psychology ; Gels ; Genes. Genome ; Genetic loci ; Genomes ; Genomics ; Heterozygote ; Human Genome Project ; Humans ; Landmarks ; Molecular and cellular biology ; Molecular genetics ; Restriction Mapping</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1991-11, Vol.88 (21), p.9523-9527</ispartof><rights>Copyright 1991 The National Academy of Sciences of the United States of America</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c588t-479960b4cf97b70fff4a39ae8e6f3b713943823b6e1ce45cab5a0a8e332c8de63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/88/21.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2357835$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2357835$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27900,27901,53765,53767,58212,58445</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5060358$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1946366$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hatada, Izuho</creatorcontrib><creatorcontrib>Hayashizaki, Yoshihide</creatorcontrib><creatorcontrib>Hirotsune, Shinji</creatorcontrib><creatorcontrib>Komatsubara, Hideyuki</creatorcontrib><creatorcontrib>Mukai, Tsunehiro</creatorcontrib><title>A Genomic Scanning Method for Higher Organisms Using Restriction Sites as Landmarks</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>We have developed a powerful genomic scanning method, termed "restriction landmark genomic scanning," that is useful for analysis of the genomic DNA of higher organisms using restriction sites as landmarks. Genomic DNA is radioactively labeled at cleavage sites specific for a rare cleaving restriction enzyme and then size-fractionated in one dimension. The fractionated DNA is further digested with another more frequently occurring enzyme and separated in the second dimension. This procedure gives a two-dimensional pattern with thousands of scattered spots corresponding to sites for the first enzyme, indicating that the genome of mammals can be scanned at ≈1-megabase intervals. The position and intensity of a spot reflect its locus and the copy number of the corresponding restriction site, respectively, based on the nature of the end-labeling system. Therefore, this method is widely applicable to genome mapping or detection of alterations in a genome.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chromosome Mapping</subject><subject>Cloning, Molecular</subject><subject>DNA</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - genetics</subject><subject>Electrophoresis</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>Enzymes</subject><subject>Fractionation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>Genes. Genome</subject><subject>Genetic loci</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Heterozygote</subject><subject>Human Genome Project</subject><subject>Humans</subject><subject>Landmarks</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Restriction Mapping</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNqFkUtvEzEUhS0EKmlhzQaQFxWsJvX7IbGpKmiRgioRurY8jp24zNjBniD498woIdANrO7ifOfce3UAeIHRHCNJL7bJ1rlSc4LnmhP6CMww0rgRTKPHYIYQkY1ihD0Fp7XeI4Q0V-gEnGDNBBViBpaX8Nqn3EcHl86mFNMafvLDJq9gyAXexPXGF3hb1jbF2ld4Vyfis69DiW6IOcFlHHyFtsKFTavelq_1GXgSbFf988M8A3cf3n-5umkWt9cfry4XjeNKDQ2TWgvUMhe0bCUKITBLtfXKi0BbialmVBHaCo-dZ9zZlltklaeUOLXygp6Bd_vc7a7t_cr5NBTbmW2J4xk_TbbRPFRS3Jh1_m44kRyN9jcHe8nfduNHpo_V-a6zyeddNZIwIRDm_wWxQIITNiVe7EFXcq3Fh-MtGJmpLjPVZZQyBJuprtHx6u8X_vD7fkb9_KDb6mwXik0u1iPGkUCUqxF7fcCm_N_qgz1v_wmYsOu6wf8YRvLlnryvQy5HlFAuFeX0F8ZpwEw</recordid><startdate>19911101</startdate><enddate>19911101</enddate><creator>Hatada, Izuho</creator><creator>Hayashizaki, Yoshihide</creator><creator>Hirotsune, Shinji</creator><creator>Komatsubara, Hideyuki</creator><creator>Mukai, Tsunehiro</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><scope>IQODW</scope><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>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19911101</creationdate><title>A Genomic Scanning Method for Higher Organisms Using Restriction Sites as Landmarks</title><author>Hatada, Izuho ; Hayashizaki, Yoshihide ; Hirotsune, Shinji ; Komatsubara, Hideyuki ; Mukai, Tsunehiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c588t-479960b4cf97b70fff4a39ae8e6f3b713943823b6e1ce45cab5a0a8e332c8de63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chromosome Mapping</topic><topic>Cloning, Molecular</topic><topic>DNA</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - genetics</topic><topic>Electrophoresis</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Enzymes</topic><topic>Fractionation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>Genes. Genome</topic><topic>Genetic loci</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Heterozygote</topic><topic>Human Genome Project</topic><topic>Humans</topic><topic>Landmarks</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Restriction Mapping</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hatada, Izuho</creatorcontrib><creatorcontrib>Hayashizaki, Yoshihide</creatorcontrib><creatorcontrib>Hirotsune, Shinji</creatorcontrib><creatorcontrib>Komatsubara, Hideyuki</creatorcontrib><creatorcontrib>Mukai, Tsunehiro</creatorcontrib><collection>Pascal-Francis</collection><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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hatada, Izuho</au><au>Hayashizaki, Yoshihide</au><au>Hirotsune, Shinji</au><au>Komatsubara, Hideyuki</au><au>Mukai, Tsunehiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Genomic Scanning Method for Higher Organisms Using Restriction Sites as Landmarks</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1991-11-01</date><risdate>1991</risdate><volume>88</volume><issue>21</issue><spage>9523</spage><epage>9527</epage><pages>9523-9527</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>We have developed a powerful genomic scanning method, termed "restriction landmark genomic scanning," that is useful for analysis of the genomic DNA of higher organisms using restriction sites as landmarks. Genomic DNA is radioactively labeled at cleavage sites specific for a rare cleaving restriction enzyme and then size-fractionated in one dimension. The fractionated DNA is further digested with another more frequently occurring enzyme and separated in the second dimension. This procedure gives a two-dimensional pattern with thousands of scattered spots corresponding to sites for the first enzyme, indicating that the genome of mammals can be scanned at ≈1-megabase intervals. The position and intensity of a spot reflect its locus and the copy number of the corresponding restriction site, respectively, based on the nature of the end-labeling system. Therefore, this method is widely applicable to genome mapping or detection of alterations in a genome.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>1946366</pmid><doi>10.1073/pnas.88.21.9523</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Chromosome Mapping Cloning, Molecular DNA Drosophila Drosophila melanogaster - genetics Electrophoresis Electrophoresis, Gel, Two-Dimensional Enzymes Fractionation Fundamental and applied biological sciences. Psychology Gels Genes. Genome Genetic loci Genomes Genomics Heterozygote Human Genome Project Humans Landmarks Molecular and cellular biology Molecular genetics Restriction Mapping |
title | A Genomic Scanning Method for Higher Organisms Using Restriction Sites as Landmarks |
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