Loading…
Construction and characterization of a large insert porcine YAC library
The recent construction of genetic linkage maps of the porcine genome allows the assignment of loci affecting heritable traits of economic importance (ETLs) to specific chromosomal segments. Markers can thus be identified that may be useful in marker-assisted selection (MAS) to increase the frequenc...
Saved in:
Published in: | Mammalian genome 1997-01, Vol.8 (1), p.50-51 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3 |
---|---|
cites | cdi_FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3 |
container_end_page | 51 |
container_issue | 1 |
container_start_page | 50 |
container_title | Mammalian genome |
container_volume | 8 |
creator | Alexander, L J Smith, T P Beattie, C W Broom, M F |
description | The recent construction of genetic linkage maps of the porcine genome allows the assignment of loci affecting heritable traits of economic importance (ETLs) to specific chromosomal segments. Markers can thus be identified that may be useful in marker-assisted selection (MAS) to increase the frequency of favorable allele(s) in resource populations. In addition, mapping of these loci creates the opportunity to identify gene(s) influencing a trait, through positional cloning or positional candidate gene approaches. A positional cloning strategy requires the construction of contigs that physically span large sections of chromosomes. In the human and mouse systems, contig construction has depended on the availability of multiple YAC libraries that provide depth of coverage to minimize the impact of chimeric and deleted clones inherent in these libraries. A single porcine genomic YAC library has been reported, but contains only one genome coverage, which limits the ability to make large contigs. We report the construction of a porcine YAC library, with approximately 5.5-fold coverage of the genome and a low rate of chimerism, that provides an additional resource for contig construction and positional cloning. |
doi_str_mv | 10.1007/s003359900347 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_853475742</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>853475742</sourcerecordid><originalsourceid>FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3</originalsourceid><addsrcrecordid>eNqF0T1PwzAQBmALgUopjIxIFgNMAZ8_4nisKihIlVhgYIpsx4FUaVzsZIBfj0srJBhgOsn3-GTfi9ApkCsgRF5HQhgTSqXC5R4aA2c0AynlPhoTxYqsSL1DdBTjkhCQOcgRGilCAQQZo_nMd7EPg-0b32HdVdi-6qBt70Lzob8OfY01bnV4cbjpogs9Xvtgm87h5-kMt40JOrwfo4Nat9Gd7OoEPd3ePM7ussXD_H42XWSWF6zPjBNgcqkF0RY2L7WuqrgiqZkbyk1leEW05sC0MFrUupacUgnKcVCUVmyCLrdz18G_DS725aqJ1rWt7pwfYlmItAWRLiV58aeURUEpkPxfCEJxELlI8PwXXPohdOm7pVRUyAIUSyjbIht8jMHV5To0q7ShEki5Caz8EVjyZ7uhg1m56lvvEmKfacqOXA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>792578193</pqid></control><display><type>article</type><title>Construction and characterization of a large insert porcine YAC library</title><source>Springer Nature</source><creator>Alexander, L J ; Smith, T P ; Beattie, C W ; Broom, M F</creator><creatorcontrib>Alexander, L J ; Smith, T P ; Beattie, C W ; Broom, M F</creatorcontrib><description>The recent construction of genetic linkage maps of the porcine genome allows the assignment of loci affecting heritable traits of economic importance (ETLs) to specific chromosomal segments. Markers can thus be identified that may be useful in marker-assisted selection (MAS) to increase the frequency of favorable allele(s) in resource populations. In addition, mapping of these loci creates the opportunity to identify gene(s) influencing a trait, through positional cloning or positional candidate gene approaches. A positional cloning strategy requires the construction of contigs that physically span large sections of chromosomes. In the human and mouse systems, contig construction has depended on the availability of multiple YAC libraries that provide depth of coverage to minimize the impact of chimeric and deleted clones inherent in these libraries. A single porcine genomic YAC library has been reported, but contains only one genome coverage, which limits the ability to make large contigs. We report the construction of a porcine YAC library, with approximately 5.5-fold coverage of the genome and a low rate of chimerism, that provides an additional resource for contig construction and positional cloning.</description><identifier>ISSN: 0938-8990</identifier><identifier>EISSN: 1432-1777</identifier><identifier>DOI: 10.1007/s003359900347</identifier><identifier>PMID: 9021150</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Animals ; Chromosomes, Artificial, Yeast ; Gene Library ; Saccharomyces cerevisiae - genetics ; Swine - genetics</subject><ispartof>Mammalian genome, 1997-01, Vol.8 (1), p.50-51</ispartof><rights>Springer-Verlag 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3</citedby><cites>FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3</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/9021150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alexander, L J</creatorcontrib><creatorcontrib>Smith, T P</creatorcontrib><creatorcontrib>Beattie, C W</creatorcontrib><creatorcontrib>Broom, M F</creatorcontrib><title>Construction and characterization of a large insert porcine YAC library</title><title>Mammalian genome</title><addtitle>Mamm Genome</addtitle><description>The recent construction of genetic linkage maps of the porcine genome allows the assignment of loci affecting heritable traits of economic importance (ETLs) to specific chromosomal segments. Markers can thus be identified that may be useful in marker-assisted selection (MAS) to increase the frequency of favorable allele(s) in resource populations. In addition, mapping of these loci creates the opportunity to identify gene(s) influencing a trait, through positional cloning or positional candidate gene approaches. A positional cloning strategy requires the construction of contigs that physically span large sections of chromosomes. In the human and mouse systems, contig construction has depended on the availability of multiple YAC libraries that provide depth of coverage to minimize the impact of chimeric and deleted clones inherent in these libraries. A single porcine genomic YAC library has been reported, but contains only one genome coverage, which limits the ability to make large contigs. We report the construction of a porcine YAC library, with approximately 5.5-fold coverage of the genome and a low rate of chimerism, that provides an additional resource for contig construction and positional cloning.</description><subject>Animals</subject><subject>Chromosomes, Artificial, Yeast</subject><subject>Gene Library</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Swine - genetics</subject><issn>0938-8990</issn><issn>1432-1777</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqF0T1PwzAQBmALgUopjIxIFgNMAZ8_4nisKihIlVhgYIpsx4FUaVzsZIBfj0srJBhgOsn3-GTfi9ApkCsgRF5HQhgTSqXC5R4aA2c0AynlPhoTxYqsSL1DdBTjkhCQOcgRGilCAQQZo_nMd7EPg-0b32HdVdi-6qBt70Lzob8OfY01bnV4cbjpogs9Xvtgm87h5-kMt40JOrwfo4Nat9Gd7OoEPd3ePM7ussXD_H42XWSWF6zPjBNgcqkF0RY2L7WuqrgiqZkbyk1leEW05sC0MFrUupacUgnKcVCUVmyCLrdz18G_DS725aqJ1rWt7pwfYlmItAWRLiV58aeURUEpkPxfCEJxELlI8PwXXPohdOm7pVRUyAIUSyjbIht8jMHV5To0q7ShEki5Caz8EVjyZ7uhg1m56lvvEmKfacqOXA</recordid><startdate>199701</startdate><enddate>199701</enddate><creator>Alexander, L J</creator><creator>Smith, T P</creator><creator>Beattie, C W</creator><creator>Broom, M F</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>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</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>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>199701</creationdate><title>Construction and characterization of a large insert porcine YAC library</title><author>Alexander, L J ; Smith, T P ; Beattie, C W ; Broom, M F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Chromosomes, Artificial, Yeast</topic><topic>Gene Library</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Swine - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alexander, L J</creatorcontrib><creatorcontrib>Smith, T P</creatorcontrib><creatorcontrib>Beattie, C W</creatorcontrib><creatorcontrib>Broom, M F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Mammalian genome</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alexander, L J</au><au>Smith, T P</au><au>Beattie, C W</au><au>Broom, M F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction and characterization of a large insert porcine YAC library</atitle><jtitle>Mammalian genome</jtitle><addtitle>Mamm Genome</addtitle><date>1997-01</date><risdate>1997</risdate><volume>8</volume><issue>1</issue><spage>50</spage><epage>51</epage><pages>50-51</pages><issn>0938-8990</issn><eissn>1432-1777</eissn><abstract>The recent construction of genetic linkage maps of the porcine genome allows the assignment of loci affecting heritable traits of economic importance (ETLs) to specific chromosomal segments. Markers can thus be identified that may be useful in marker-assisted selection (MAS) to increase the frequency of favorable allele(s) in resource populations. In addition, mapping of these loci creates the opportunity to identify gene(s) influencing a trait, through positional cloning or positional candidate gene approaches. A positional cloning strategy requires the construction of contigs that physically span large sections of chromosomes. In the human and mouse systems, contig construction has depended on the availability of multiple YAC libraries that provide depth of coverage to minimize the impact of chimeric and deleted clones inherent in these libraries. A single porcine genomic YAC library has been reported, but contains only one genome coverage, which limits the ability to make large contigs. We report the construction of a porcine YAC library, with approximately 5.5-fold coverage of the genome and a low rate of chimerism, that provides an additional resource for contig construction and positional cloning.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>9021150</pmid><doi>10.1007/s003359900347</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0938-8990 |
ispartof | Mammalian genome, 1997-01, Vol.8 (1), p.50-51 |
issn | 0938-8990 1432-1777 |
language | eng |
recordid | cdi_proquest_miscellaneous_853475742 |
source | Springer Nature |
subjects | Animals Chromosomes, Artificial, Yeast Gene Library Saccharomyces cerevisiae - genetics Swine - genetics |
title | Construction and characterization of a large insert porcine YAC library |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T06%3A41%3A32IST&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=Construction%20and%20characterization%20of%20a%20large%20insert%20porcine%20YAC%20library&rft.jtitle=Mammalian%20genome&rft.au=Alexander,%20L%20J&rft.date=1997-01&rft.volume=8&rft.issue=1&rft.spage=50&rft.epage=51&rft.pages=50-51&rft.issn=0938-8990&rft.eissn=1432-1777&rft_id=info:doi/10.1007/s003359900347&rft_dat=%3Cproquest_cross%3E853475742%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c483t-be51b67a50ac11432cedd4904836b24bdb4d0aa413a5ba5faf7422719e41922d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=792578193&rft_id=info:pmid/9021150&rfr_iscdi=true |