Targeting of non-lg sequences in place of the V segment by somatic hyper mutation

Affinity maturation of antibodies is characterized by localized hypermutation of the DNA around the V segment. Here we show, using mice containing single or multiple transgene constructs, that an immunoglobulin V K segment can be replaced by human β-globin or prokaryotic neo or gpt genes without aff...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature (London) 1995-07, Vol.376 (6537), p.225-229
Hauptverfasser: Yélamos, J., Klix, N., Goyenechea, B., Lozano, F., Chui, Y. L., FernÃndez, A. GonzÃlez, Pannell, R., Neuberger, M. S., Milstein, C.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 229
container_issue 6537
container_start_page 225
container_title Nature (London)
container_volume 376
creator Yélamos, J.
Klix, N.
Goyenechea, B.
Lozano, F.
Chui, Y. L.
FernÃndez, A. GonzÃlez
Pannell, R.
Neuberger, M. S.
Milstein, C.
description Affinity maturation of antibodies is characterized by localized hypermutation of the DNA around the V segment. Here we show, using mice containing single or multiple transgene constructs, that an immunoglobulin V K segment can be replaced by human β-globin or prokaryotic neo or gpt genes without affecting the rate of hypermutation; the V gene itself is not necessary for recruiting hypermutation. The ability to target hypermutation to heterologous genes in vivo could find more general applications in biology.
doi_str_mv 10.1038/376225a0
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_856762393</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>856762393</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3420-643e0a5d91ed8e30e2374297e1d9165e7f5d3d75ded6d924a97999a7aec232863</originalsourceid><addsrcrecordid>eNplkE1LxDAQhoMouH6APyE39VDNR5s0R1n8ggURVq8hJtNulzapSXvYf2-W1ZOnYeZ9GGYehK4ouaOE1_dcCsYqQ47QgpZSFKWo5TFaEMLqgtRcnKKzlLaEkIrKcoHe1ya2MHW-xaHBPviib3GC7xm8hYQ7j8feWNiH0wbwZ87aAfyEv3Y4hcFMncWb3QgRD_OUu-Av0Elj-gSXv_UcfTw9rpcvxert-XX5sCosLxkpRMmBmMopCq4GToBxWTIlgeaRqEA2leNOVg6ccIqVRkmllJEGLOOsFvwcXR_2jjHkc9Okhy5Z6HvjIcxJ15XIKrjimbw5kDaGlCI0eozdYOJOU6L30vSftIzeHtCUEd9C1NswR5__-M_-AANkau8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>856762393</pqid></control><display><type>article</type><title>Targeting of non-lg sequences in place of the V segment by somatic hyper mutation</title><source>Springer Nature - Complete Springer Journals</source><source>Nature Journals Online</source><creator>Yélamos, J. ; Klix, N. ; Goyenechea, B. ; Lozano, F. ; Chui, Y. L. ; FernÃndez, A. GonzÃlez ; Pannell, R. ; Neuberger, M. S. ; Milstein, C.</creator><creatorcontrib>Yélamos, J. ; Klix, N. ; Goyenechea, B. ; Lozano, F. ; Chui, Y. L. ; FernÃndez, A. GonzÃlez ; Pannell, R. ; Neuberger, M. S. ; Milstein, C.</creatorcontrib><description>Affinity maturation of antibodies is characterized by localized hypermutation of the DNA around the V segment. Here we show, using mice containing single or multiple transgene constructs, that an immunoglobulin V K segment can be replaced by human β-globin or prokaryotic neo or gpt genes without affecting the rate of hypermutation; the V gene itself is not necessary for recruiting hypermutation. The ability to target hypermutation to heterologous genes in vivo could find more general applications in biology.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/376225a0</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Humanities and Social Sciences ; multidisciplinary ; Science ; Science (multidisciplinary)</subject><ispartof>Nature (London), 1995-07, Vol.376 (6537), p.225-229</ispartof><rights>Springer Nature Limited 1995</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3420-643e0a5d91ed8e30e2374297e1d9165e7f5d3d75ded6d924a97999a7aec232863</citedby><cites>FETCH-LOGICAL-c3420-643e0a5d91ed8e30e2374297e1d9165e7f5d3d75ded6d924a97999a7aec232863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/376225a0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/376225a0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Yélamos, J.</creatorcontrib><creatorcontrib>Klix, N.</creatorcontrib><creatorcontrib>Goyenechea, B.</creatorcontrib><creatorcontrib>Lozano, F.</creatorcontrib><creatorcontrib>Chui, Y. L.</creatorcontrib><creatorcontrib>FernÃndez, A. GonzÃlez</creatorcontrib><creatorcontrib>Pannell, R.</creatorcontrib><creatorcontrib>Neuberger, M. S.</creatorcontrib><creatorcontrib>Milstein, C.</creatorcontrib><title>Targeting of non-lg sequences in place of the V segment by somatic hyper mutation</title><title>Nature (London)</title><addtitle>Nature</addtitle><description>Affinity maturation of antibodies is characterized by localized hypermutation of the DNA around the V segment. Here we show, using mice containing single or multiple transgene constructs, that an immunoglobulin V K segment can be replaced by human β-globin or prokaryotic neo or gpt genes without affecting the rate of hypermutation; the V gene itself is not necessary for recruiting hypermutation. The ability to target hypermutation to heterologous genes in vivo could find more general applications in biology.</description><subject>Humanities and Social Sciences</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNplkE1LxDAQhoMouH6APyE39VDNR5s0R1n8ggURVq8hJtNulzapSXvYf2-W1ZOnYeZ9GGYehK4ouaOE1_dcCsYqQ47QgpZSFKWo5TFaEMLqgtRcnKKzlLaEkIrKcoHe1ya2MHW-xaHBPviib3GC7xm8hYQ7j8feWNiH0wbwZ87aAfyEv3Y4hcFMncWb3QgRD_OUu-Av0Elj-gSXv_UcfTw9rpcvxert-XX5sCosLxkpRMmBmMopCq4GToBxWTIlgeaRqEA2leNOVg6ccIqVRkmllJEGLOOsFvwcXR_2jjHkc9Okhy5Z6HvjIcxJ15XIKrjimbw5kDaGlCI0eozdYOJOU6L30vSftIzeHtCUEd9C1NswR5__-M_-AANkau8</recordid><startdate>19950701</startdate><enddate>19950701</enddate><creator>Yélamos, J.</creator><creator>Klix, N.</creator><creator>Goyenechea, B.</creator><creator>Lozano, F.</creator><creator>Chui, Y. L.</creator><creator>FernÃndez, A. GonzÃlez</creator><creator>Pannell, R.</creator><creator>Neuberger, M. S.</creator><creator>Milstein, C.</creator><general>Nature Publishing Group UK</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19950701</creationdate><title>Targeting of non-lg sequences in place of the V segment by somatic hyper mutation</title><author>Yélamos, J. ; Klix, N. ; Goyenechea, B. ; Lozano, F. ; Chui, Y. L. ; FernÃndez, A. GonzÃlez ; Pannell, R. ; Neuberger, M. S. ; Milstein, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3420-643e0a5d91ed8e30e2374297e1d9165e7f5d3d75ded6d924a97999a7aec232863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Humanities and Social Sciences</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yélamos, J.</creatorcontrib><creatorcontrib>Klix, N.</creatorcontrib><creatorcontrib>Goyenechea, B.</creatorcontrib><creatorcontrib>Lozano, F.</creatorcontrib><creatorcontrib>Chui, Y. L.</creatorcontrib><creatorcontrib>FernÃndez, A. GonzÃlez</creatorcontrib><creatorcontrib>Pannell, R.</creatorcontrib><creatorcontrib>Neuberger, M. S.</creatorcontrib><creatorcontrib>Milstein, C.</creatorcontrib><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yélamos, J.</au><au>Klix, N.</au><au>Goyenechea, B.</au><au>Lozano, F.</au><au>Chui, Y. L.</au><au>FernÃndez, A. GonzÃlez</au><au>Pannell, R.</au><au>Neuberger, M. S.</au><au>Milstein, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting of non-lg sequences in place of the V segment by somatic hyper mutation</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><date>1995-07-01</date><risdate>1995</risdate><volume>376</volume><issue>6537</issue><spage>225</spage><epage>229</epage><pages>225-229</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>Affinity maturation of antibodies is characterized by localized hypermutation of the DNA around the V segment. Here we show, using mice containing single or multiple transgene constructs, that an immunoglobulin V K segment can be replaced by human β-globin or prokaryotic neo or gpt genes without affecting the rate of hypermutation; the V gene itself is not necessary for recruiting hypermutation. The ability to target hypermutation to heterologous genes in vivo could find more general applications in biology.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/376225a0</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0028-0836
ispartof Nature (London), 1995-07, Vol.376 (6537), p.225-229
issn 0028-0836
1476-4687
language eng
recordid cdi_proquest_miscellaneous_856762393
source Springer Nature - Complete Springer Journals; Nature Journals Online
subjects Humanities and Social Sciences
multidisciplinary
Science
Science (multidisciplinary)
title Targeting of non-lg sequences in place of the V segment by somatic hyper mutation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T18%3A35%3A24IST&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=Targeting%20of%20non-lg%20sequences%20in%20place%20of%20the%20V%20segment%20by%20somatic%20hyper%20mutation&rft.jtitle=Nature%20(London)&rft.au=Y%C3%83%C2%A9lamos,%20J.&rft.date=1995-07-01&rft.volume=376&rft.issue=6537&rft.spage=225&rft.epage=229&rft.pages=225-229&rft.issn=0028-0836&rft.eissn=1476-4687&rft_id=info:doi/10.1038/376225a0&rft_dat=%3Cproquest_cross%3E856762393%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=856762393&rft_id=info:pmid/&rfr_iscdi=true