Loading…
Transmission of mutations in the lacI transgene to the offspring of ENU-treated Big Blue® male mice
The purpose of the study was to determine: 1) if male germ cells of Big Blue® mice carrying newly induced mutations in the lacI transgene were effective in fertilization; 2) if offspring arising from such mutant sperm had the mutation in germ cells and multiple somatic tissues; and 3) how the freque...
Saved in:
Published in: | Environmental and molecular mutagenesis 2002, Vol.40 (4), p.251-257 |
---|---|
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-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63 |
---|---|
cites | cdi_FETCH-LOGICAL-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63 |
container_end_page | 257 |
container_issue | 4 |
container_start_page | 251 |
container_title | Environmental and molecular mutagenesis |
container_volume | 40 |
creator | Barnett, Lois B. Tyl, Rochelle W. Shane, Barbara S. Shelby, Michael D. Lewis, Susan E. |
description | The purpose of the study was to determine: 1) if male germ cells of Big Blue® mice carrying newly induced mutations in the lacI transgene were effective in fertilization; 2) if offspring arising from such mutant sperm had the mutation in germ cells and multiple somatic tissues; and 3) how the frequency of mutants induced in the lacI transgene compared to the frequency induced in endogenous genes traditionally employed to study germ cell mutagenesis in mice. Male B6C3F1 mice hemizygous for the lambda/lacI transgene were treated weekly with 100 mg/kg body weight of the mammalian germ cell mutagen N‐ethyl‐N‐nitrosourea (ENU). The cumulative dose for each treated animal was 300 mg ENU/kg body weight. Ten weeks later the treated mice were mated to T stock females and the resulting offspring were screened for specific‐locus mutations at six loci affecting external appearance, as well as for mutations in the lacI transgene in multiple somatic tissues and germ cells. Five offspring carrying recessive specific‐locus mutations were observed among 597 offspring screened (mutant frequency = 139.6 × 10‐5 per locus). Four offspring carrying lacI mutations were observed among 280 offspring screened (mutant frequency = 35.7 × 10‐5 per locus (assuming 40 target loci)). Each of the four lacI mutant offspring carried a different mutation. Three of the mutations were A:T→G:C transitions and one a G:C→A:T transition. Consistent with the expectation that a mutation induced in a parental germ cell and transmitted to a conceptus would exist in every cell of the offspring, each mutant mouse had identical mutations in all somatic tissues sampled, as well as in its germ cells. These data provide preliminary evidence for the biological validity of assessing induced, heritable mutations using transgenic mice, without the need for generating an F1 generation. Environ. Mol. Mutagen. 40:251–257, 2002. © 2002 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/em.10114 |
format | article |
fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_em_10114</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_H16LS56K_K</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63</originalsourceid><addsrcrecordid>eNp10MtOAjEUBuDGaATRxCcwXboZ7WWm0y6FIBAQF0JcNmXmDFbnQqYlykv5ED6Zw0VduTpN8_VPz4_QJSU3lBB2C0UzKQ2PUJsSJQPGJDlGbSIVD4RQrIXOnHslW6LYKWpRFkpFadRG6aw2pSusc7YqcZXhYu2Nb84O2xL7F8C5SUbYb9USSsC-2t1WWeZWtS2X2zf96TzwNRgPKe7aJe7ma_j6xIXJARc2gXN0kpncwcVhdtD8vj_rDYPJ42DUu5sECeciDGQYq1BSUDQRnEqeJjEhhidRDGkkjFRMpAxIpuIsirlZ8IiFQARrlsoUTwXvoOt9blJXztWQ6eaLhak3mhK9LUpDoXdFNfRqT1frRQHpHzw004BgD95tDpt_g3T_4Sfw4K3z8PHrTf2mRczjSD9PB3pIxeQpEmM95t9qz39k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Transmission of mutations in the lacI transgene to the offspring of ENU-treated Big Blue® male mice</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Barnett, Lois B. ; Tyl, Rochelle W. ; Shane, Barbara S. ; Shelby, Michael D. ; Lewis, Susan E.</creator><creatorcontrib>Barnett, Lois B. ; Tyl, Rochelle W. ; Shane, Barbara S. ; Shelby, Michael D. ; Lewis, Susan E.</creatorcontrib><description>The purpose of the study was to determine: 1) if male germ cells of Big Blue® mice carrying newly induced mutations in the lacI transgene were effective in fertilization; 2) if offspring arising from such mutant sperm had the mutation in germ cells and multiple somatic tissues; and 3) how the frequency of mutants induced in the lacI transgene compared to the frequency induced in endogenous genes traditionally employed to study germ cell mutagenesis in mice. Male B6C3F1 mice hemizygous for the lambda/lacI transgene were treated weekly with 100 mg/kg body weight of the mammalian germ cell mutagen N‐ethyl‐N‐nitrosourea (ENU). The cumulative dose for each treated animal was 300 mg ENU/kg body weight. Ten weeks later the treated mice were mated to T stock females and the resulting offspring were screened for specific‐locus mutations at six loci affecting external appearance, as well as for mutations in the lacI transgene in multiple somatic tissues and germ cells. Five offspring carrying recessive specific‐locus mutations were observed among 597 offspring screened (mutant frequency = 139.6 × 10‐5 per locus). Four offspring carrying lacI mutations were observed among 280 offspring screened (mutant frequency = 35.7 × 10‐5 per locus (assuming 40 target loci)). Each of the four lacI mutant offspring carried a different mutation. Three of the mutations were A:T→G:C transitions and one a G:C→A:T transition. Consistent with the expectation that a mutation induced in a parental germ cell and transmitted to a conceptus would exist in every cell of the offspring, each mutant mouse had identical mutations in all somatic tissues sampled, as well as in its germ cells. These data provide preliminary evidence for the biological validity of assessing induced, heritable mutations using transgenic mice, without the need for generating an F1 generation. Environ. Mol. Mutagen. 40:251–257, 2002. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 0893-6692</identifier><identifier>EISSN: 1098-2280</identifier><identifier>DOI: 10.1002/em.10114</identifier><identifier>PMID: 12489115</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Bacterial Proteins ; Crosses, Genetic ; DNA Mutational Analysis ; Escherichia coli Proteins - genetics ; Ethylnitrosourea - pharmacology ; Female ; germ cell mutagenesis ; Germ-Line Mutation ; Lac Repressors ; lacI transgenic mice ; Male ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Mice, Transgenic ; Mutagens - pharmacology ; Mutation ; N-ethyl-N-nitrosourea ; Repressor Proteins - genetics ; Species Specificity ; specific-locus test ; Spermatozoa - drug effects ; Spleen - metabolism ; Time Factors ; Transgenes</subject><ispartof>Environmental and molecular mutagenesis, 2002, Vol.40 (4), p.251-257</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63</citedby><cites>FETCH-LOGICAL-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12489115$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barnett, Lois B.</creatorcontrib><creatorcontrib>Tyl, Rochelle W.</creatorcontrib><creatorcontrib>Shane, Barbara S.</creatorcontrib><creatorcontrib>Shelby, Michael D.</creatorcontrib><creatorcontrib>Lewis, Susan E.</creatorcontrib><title>Transmission of mutations in the lacI transgene to the offspring of ENU-treated Big Blue® male mice</title><title>Environmental and molecular mutagenesis</title><addtitle>Environ. Mol. Mutagen</addtitle><description>The purpose of the study was to determine: 1) if male germ cells of Big Blue® mice carrying newly induced mutations in the lacI transgene were effective in fertilization; 2) if offspring arising from such mutant sperm had the mutation in germ cells and multiple somatic tissues; and 3) how the frequency of mutants induced in the lacI transgene compared to the frequency induced in endogenous genes traditionally employed to study germ cell mutagenesis in mice. Male B6C3F1 mice hemizygous for the lambda/lacI transgene were treated weekly with 100 mg/kg body weight of the mammalian germ cell mutagen N‐ethyl‐N‐nitrosourea (ENU). The cumulative dose for each treated animal was 300 mg ENU/kg body weight. Ten weeks later the treated mice were mated to T stock females and the resulting offspring were screened for specific‐locus mutations at six loci affecting external appearance, as well as for mutations in the lacI transgene in multiple somatic tissues and germ cells. Five offspring carrying recessive specific‐locus mutations were observed among 597 offspring screened (mutant frequency = 139.6 × 10‐5 per locus). Four offspring carrying lacI mutations were observed among 280 offspring screened (mutant frequency = 35.7 × 10‐5 per locus (assuming 40 target loci)). Each of the four lacI mutant offspring carried a different mutation. Three of the mutations were A:T→G:C transitions and one a G:C→A:T transition. Consistent with the expectation that a mutation induced in a parental germ cell and transmitted to a conceptus would exist in every cell of the offspring, each mutant mouse had identical mutations in all somatic tissues sampled, as well as in its germ cells. These data provide preliminary evidence for the biological validity of assessing induced, heritable mutations using transgenic mice, without the need for generating an F1 generation. Environ. Mol. Mutagen. 40:251–257, 2002. © 2002 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Bacterial Proteins</subject><subject>Crosses, Genetic</subject><subject>DNA Mutational Analysis</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Ethylnitrosourea - pharmacology</subject><subject>Female</subject><subject>germ cell mutagenesis</subject><subject>Germ-Line Mutation</subject><subject>Lac Repressors</subject><subject>lacI transgenic mice</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Mutagens - pharmacology</subject><subject>Mutation</subject><subject>N-ethyl-N-nitrosourea</subject><subject>Repressor Proteins - genetics</subject><subject>Species Specificity</subject><subject>specific-locus test</subject><subject>Spermatozoa - drug effects</subject><subject>Spleen - metabolism</subject><subject>Time Factors</subject><subject>Transgenes</subject><issn>0893-6692</issn><issn>1098-2280</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp10MtOAjEUBuDGaATRxCcwXboZ7WWm0y6FIBAQF0JcNmXmDFbnQqYlykv5ED6Zw0VduTpN8_VPz4_QJSU3lBB2C0UzKQ2PUJsSJQPGJDlGbSIVD4RQrIXOnHslW6LYKWpRFkpFadRG6aw2pSusc7YqcZXhYu2Nb84O2xL7F8C5SUbYb9USSsC-2t1WWeZWtS2X2zf96TzwNRgPKe7aJe7ma_j6xIXJARc2gXN0kpncwcVhdtD8vj_rDYPJ42DUu5sECeciDGQYq1BSUDQRnEqeJjEhhidRDGkkjFRMpAxIpuIsirlZ8IiFQARrlsoUTwXvoOt9blJXztWQ6eaLhak3mhK9LUpDoXdFNfRqT1frRQHpHzw004BgD95tDpt_g3T_4Sfw4K3z8PHrTf2mRczjSD9PB3pIxeQpEmM95t9qz39k</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Barnett, Lois B.</creator><creator>Tyl, Rochelle W.</creator><creator>Shane, Barbara S.</creator><creator>Shelby, Michael D.</creator><creator>Lewis, Susan E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>2002</creationdate><title>Transmission of mutations in the lacI transgene to the offspring of ENU-treated Big Blue® male mice</title><author>Barnett, Lois B. ; Tyl, Rochelle W. ; Shane, Barbara S. ; Shelby, Michael D. ; Lewis, Susan E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Bacterial Proteins</topic><topic>Crosses, Genetic</topic><topic>DNA Mutational Analysis</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Ethylnitrosourea - pharmacology</topic><topic>Female</topic><topic>germ cell mutagenesis</topic><topic>Germ-Line Mutation</topic><topic>Lac Repressors</topic><topic>lacI transgenic mice</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Mutagens - pharmacology</topic><topic>Mutation</topic><topic>N-ethyl-N-nitrosourea</topic><topic>Repressor Proteins - genetics</topic><topic>Species Specificity</topic><topic>specific-locus test</topic><topic>Spermatozoa - drug effects</topic><topic>Spleen - metabolism</topic><topic>Time Factors</topic><topic>Transgenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barnett, Lois B.</creatorcontrib><creatorcontrib>Tyl, Rochelle W.</creatorcontrib><creatorcontrib>Shane, Barbara S.</creatorcontrib><creatorcontrib>Shelby, Michael D.</creatorcontrib><creatorcontrib>Lewis, Susan E.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Environmental and molecular mutagenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barnett, Lois B.</au><au>Tyl, Rochelle W.</au><au>Shane, Barbara S.</au><au>Shelby, Michael D.</au><au>Lewis, Susan E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transmission of mutations in the lacI transgene to the offspring of ENU-treated Big Blue® male mice</atitle><jtitle>Environmental and molecular mutagenesis</jtitle><addtitle>Environ. Mol. Mutagen</addtitle><date>2002</date><risdate>2002</risdate><volume>40</volume><issue>4</issue><spage>251</spage><epage>257</epage><pages>251-257</pages><issn>0893-6692</issn><eissn>1098-2280</eissn><abstract>The purpose of the study was to determine: 1) if male germ cells of Big Blue® mice carrying newly induced mutations in the lacI transgene were effective in fertilization; 2) if offspring arising from such mutant sperm had the mutation in germ cells and multiple somatic tissues; and 3) how the frequency of mutants induced in the lacI transgene compared to the frequency induced in endogenous genes traditionally employed to study germ cell mutagenesis in mice. Male B6C3F1 mice hemizygous for the lambda/lacI transgene were treated weekly with 100 mg/kg body weight of the mammalian germ cell mutagen N‐ethyl‐N‐nitrosourea (ENU). The cumulative dose for each treated animal was 300 mg ENU/kg body weight. Ten weeks later the treated mice were mated to T stock females and the resulting offspring were screened for specific‐locus mutations at six loci affecting external appearance, as well as for mutations in the lacI transgene in multiple somatic tissues and germ cells. Five offspring carrying recessive specific‐locus mutations were observed among 597 offspring screened (mutant frequency = 139.6 × 10‐5 per locus). Four offspring carrying lacI mutations were observed among 280 offspring screened (mutant frequency = 35.7 × 10‐5 per locus (assuming 40 target loci)). Each of the four lacI mutant offspring carried a different mutation. Three of the mutations were A:T→G:C transitions and one a G:C→A:T transition. Consistent with the expectation that a mutation induced in a parental germ cell and transmitted to a conceptus would exist in every cell of the offspring, each mutant mouse had identical mutations in all somatic tissues sampled, as well as in its germ cells. These data provide preliminary evidence for the biological validity of assessing induced, heritable mutations using transgenic mice, without the need for generating an F1 generation. Environ. Mol. Mutagen. 40:251–257, 2002. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12489115</pmid><doi>10.1002/em.10114</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0893-6692 |
ispartof | Environmental and molecular mutagenesis, 2002, Vol.40 (4), p.251-257 |
issn | 0893-6692 1098-2280 |
language | eng |
recordid | cdi_crossref_primary_10_1002_em_10114 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Animals Bacterial Proteins Crosses, Genetic DNA Mutational Analysis Escherichia coli Proteins - genetics Ethylnitrosourea - pharmacology Female germ cell mutagenesis Germ-Line Mutation Lac Repressors lacI transgenic mice Male Mice Mice, Inbred C3H Mice, Inbred C57BL Mice, Transgenic Mutagens - pharmacology Mutation N-ethyl-N-nitrosourea Repressor Proteins - genetics Species Specificity specific-locus test Spermatozoa - drug effects Spleen - metabolism Time Factors Transgenes |
title | Transmission of mutations in the lacI transgene to the offspring of ENU-treated Big Blue® male mice |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T09%3A26%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Transmission%20of%20mutations%20in%20the%20lacI%20transgene%20to%20the%20offspring%20of%20ENU-treated%20Big%20Blue%C2%AE%20male%20mice&rft.jtitle=Environmental%20and%20molecular%20mutagenesis&rft.au=Barnett,%20Lois%20B.&rft.date=2002&rft.volume=40&rft.issue=4&rft.spage=251&rft.epage=257&rft.pages=251-257&rft.issn=0893-6692&rft.eissn=1098-2280&rft_id=info:doi/10.1002/em.10114&rft_dat=%3Cistex_cross%3Eark_67375_WNG_H16LS56K_K%3C/istex_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3364-8479481e91c63183dc700a3c57ed56a8926d2e0f97f573ab3524e062149f93d63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/12489115&rfr_iscdi=true |