MNU-induced mutant pools and high performance TILLING enable finding of any gene mutation in rice
Mutant populations are indispensable genetic resources for functional genomics in all organisms. However, suitable rice mutant populations, induced either by chemicals or irradiation still have been rarely developed to date. To produce mutant pools and to launch a search system for rice gene mutatio...
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creator | Suzuki, Tadzunu Eiguchi, Mitsugu Kumamaru, Toshihiro Satoh, Hikaru Matsusaka, Hiroaki Moriguchi, Kazuki Nagato, Yasuo Kurata, Nori |
description | Mutant populations are indispensable genetic resources for functional genomics in all organisms. However, suitable rice mutant populations, induced either by chemicals or irradiation still have been rarely developed to date. To produce mutant pools and to launch a search system for rice gene mutations, we developed mutant populations of Oryza sativa japonica cv. Taichung 65, by treating single zygotic cells with N-methyl-N-nitrosourea (MNU). Mutagenesis in single zygotes can create mutations at a high frequency and rarely forms chimeric plants. A modified TILLING system using non-labeled primers and fast capillary gel electrophoresis was applied for high-throughput detection of single nucleotide substitution mutations. The mutation rate of an M₂ mutant population was calculated as 7.4 x 10-⁶ per nucleotide representing one mutation in every 135 kb genome sequence. One can expect 7.4 single nucleotide substitution mutations in every 1 kb of gene region when using 1,000 M₂ mutant lines. The mutations were very evenly distributed over the regions examined. These results indicate that our rice mutant population generated by MNU-mutagenesis could be a promising resource for identifying mutations in any gene of rice. The modified TILLING method also proved very efficient and convenient in screening the mutant population. |
doi_str_mv | 10.1007/s00438-007-0293-2 |
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However, suitable rice mutant populations, induced either by chemicals or irradiation still have been rarely developed to date. To produce mutant pools and to launch a search system for rice gene mutations, we developed mutant populations of Oryza sativa japonica cv. Taichung 65, by treating single zygotic cells with N-methyl-N-nitrosourea (MNU). Mutagenesis in single zygotes can create mutations at a high frequency and rarely forms chimeric plants. A modified TILLING system using non-labeled primers and fast capillary gel electrophoresis was applied for high-throughput detection of single nucleotide substitution mutations. The mutation rate of an M₂ mutant population was calculated as 7.4 x 10-⁶ per nucleotide representing one mutation in every 135 kb genome sequence. One can expect 7.4 single nucleotide substitution mutations in every 1 kb of gene region when using 1,000 M₂ mutant lines. The mutations were very evenly distributed over the regions examined. These results indicate that our rice mutant population generated by MNU-mutagenesis could be a promising resource for identifying mutations in any gene of rice. The modified TILLING method also proved very efficient and convenient in screening the mutant population.</description><identifier>ISSN: 1617-4615</identifier><identifier>EISSN: 1617-4623</identifier><identifier>DOI: 10.1007/s00438-007-0293-2</identifier><identifier>PMID: 17952471</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Alleles ; Animal Genetics and Genomics ; Base Sequence ; Biochemistry ; Biomedical and Life Sciences ; DNA Mutational Analysis - methods ; DNA Primers - genetics ; DNA, Plant - genetics ; Genes ; Genes, Plant - drug effects ; Genetic Techniques ; Genetics ; Genomes ; Genomics ; Human Genetics ; Life Sciences ; Methylnitrosourea - toxicity ; Microbial Genetics and Genomics ; Mutagenesis ; Mutagens - toxicity ; Mutation ; Original Paper ; Oryza ; Oryza - drug effects ; Oryza - genetics ; Oryza sativa ; Plant Genetics and Genomics ; Polymerase Chain Reaction ; Rice ; Seeds</subject><ispartof>Molecular genetics and genomics : MGG, 2008-03, Vol.279 (3), p.213-223</ispartof><rights>Springer-Verlag 2007</rights><rights>Springer-Verlag 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-a037802300e3f992a82181c76572b14020d97bd76cc537c00f1f43dbc57e5b1a3</citedby><cites>FETCH-LOGICAL-c490t-a037802300e3f992a82181c76572b14020d97bd76cc537c00f1f43dbc57e5b1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00438-007-0293-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00438-007-0293-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17952471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Tadzunu</creatorcontrib><creatorcontrib>Eiguchi, Mitsugu</creatorcontrib><creatorcontrib>Kumamaru, Toshihiro</creatorcontrib><creatorcontrib>Satoh, Hikaru</creatorcontrib><creatorcontrib>Matsusaka, Hiroaki</creatorcontrib><creatorcontrib>Moriguchi, Kazuki</creatorcontrib><creatorcontrib>Nagato, Yasuo</creatorcontrib><creatorcontrib>Kurata, Nori</creatorcontrib><title>MNU-induced mutant pools and high performance TILLING enable finding of any gene mutation in rice</title><title>Molecular genetics and genomics : MGG</title><addtitle>Mol Genet Genomics</addtitle><addtitle>Mol Genet Genomics</addtitle><description>Mutant populations are indispensable genetic resources for functional genomics in all organisms. However, suitable rice mutant populations, induced either by chemicals or irradiation still have been rarely developed to date. To produce mutant pools and to launch a search system for rice gene mutations, we developed mutant populations of Oryza sativa japonica cv. Taichung 65, by treating single zygotic cells with N-methyl-N-nitrosourea (MNU). Mutagenesis in single zygotes can create mutations at a high frequency and rarely forms chimeric plants. A modified TILLING system using non-labeled primers and fast capillary gel electrophoresis was applied for high-throughput detection of single nucleotide substitution mutations. The mutation rate of an M₂ mutant population was calculated as 7.4 x 10-⁶ per nucleotide representing one mutation in every 135 kb genome sequence. One can expect 7.4 single nucleotide substitution mutations in every 1 kb of gene region when using 1,000 M₂ mutant lines. The mutations were very evenly distributed over the regions examined. These results indicate that our rice mutant population generated by MNU-mutagenesis could be a promising resource for identifying mutations in any gene of rice. The modified TILLING method also proved very efficient and convenient in screening the mutant population.</description><subject>Alleles</subject><subject>Animal Genetics and Genomics</subject><subject>Base Sequence</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>DNA Mutational Analysis - methods</subject><subject>DNA Primers - genetics</subject><subject>DNA, Plant - genetics</subject><subject>Genes</subject><subject>Genes, Plant - drug effects</subject><subject>Genetic Techniques</subject><subject>Genetics</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Human Genetics</subject><subject>Life Sciences</subject><subject>Methylnitrosourea - toxicity</subject><subject>Microbial Genetics and Genomics</subject><subject>Mutagenesis</subject><subject>Mutagens - toxicity</subject><subject>Mutation</subject><subject>Original Paper</subject><subject>Oryza</subject><subject>Oryza - drug effects</subject><subject>Oryza - genetics</subject><subject>Oryza sativa</subject><subject>Plant Genetics and Genomics</subject><subject>Polymerase Chain Reaction</subject><subject>Rice</subject><subject>Seeds</subject><issn>1617-4615</issn><issn>1617-4623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kE1v1DAURSMEoh_wA9iAxYJd2vdsJ06WqCrtSNOyaGdtOY6dukrswU4W_fd4yAgQC1a-ks-9tk5RfEC4QABxmQA4a8ocS6AtK-mr4hRrFCWvKXv9O2N1Upyl9AyAoqbibXGCoq0oF3haqLv7Xel8v2jTk2mZlZ_JPoQxEeV78uSGJ7I30YY4Ka8Nedxst5v7G2K86kZDbG46P5BgM_5CBuPNr5HZBU-cJ9Fp8654Y9WYzPvjeV7svl0_Xt2W2-83m6uv21LzFuZSARMNUAZgmG1bqhqKDWpRV4J2yIFC34quF7XWFRMawKLlrO90JUzVoWLnxZd1dx_Dj8WkWU4uaTOOypuwJIlt09StaDL4-R_wOSzR579lhmPNOccM4QrpGFKKxsp9dJOKLxJBHuTLVb48xIN8SXPn43F46SbT_2kcbWeArkDKV34w8a-X_7P6aS1ZFaQaokty90ABs6mmallTsZ-4lpYv</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Suzuki, Tadzunu</creator><creator>Eiguchi, Mitsugu</creator><creator>Kumamaru, Toshihiro</creator><creator>Satoh, Hikaru</creator><creator>Matsusaka, Hiroaki</creator><creator>Moriguchi, Kazuki</creator><creator>Nagato, Yasuo</creator><creator>Kurata, Nori</creator><general>Berlin/Heidelberg : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</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>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope></search><sort><creationdate>20080301</creationdate><title>MNU-induced mutant pools and high performance TILLING enable finding of any gene mutation in rice</title><author>Suzuki, Tadzunu ; Eiguchi, Mitsugu ; Kumamaru, Toshihiro ; Satoh, Hikaru ; Matsusaka, Hiroaki ; Moriguchi, Kazuki ; Nagato, Yasuo ; Kurata, Nori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-a037802300e3f992a82181c76572b14020d97bd76cc537c00f1f43dbc57e5b1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Alleles</topic><topic>Animal Genetics and Genomics</topic><topic>Base Sequence</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>DNA Mutational Analysis - methods</topic><topic>DNA Primers - genetics</topic><topic>DNA, Plant - genetics</topic><topic>Genes</topic><topic>Genes, Plant - drug effects</topic><topic>Genetic Techniques</topic><topic>Genetics</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Human Genetics</topic><topic>Life Sciences</topic><topic>Methylnitrosourea - toxicity</topic><topic>Microbial Genetics and Genomics</topic><topic>Mutagenesis</topic><topic>Mutagens - toxicity</topic><topic>Mutation</topic><topic>Original Paper</topic><topic>Oryza</topic><topic>Oryza - drug effects</topic><topic>Oryza - genetics</topic><topic>Oryza sativa</topic><topic>Plant Genetics and Genomics</topic><topic>Polymerase Chain Reaction</topic><topic>Rice</topic><topic>Seeds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Tadzunu</creatorcontrib><creatorcontrib>Eiguchi, Mitsugu</creatorcontrib><creatorcontrib>Kumamaru, Toshihiro</creatorcontrib><creatorcontrib>Satoh, Hikaru</creatorcontrib><creatorcontrib>Matsusaka, Hiroaki</creatorcontrib><creatorcontrib>Moriguchi, Kazuki</creatorcontrib><creatorcontrib>Nagato, Yasuo</creatorcontrib><creatorcontrib>Kurata, Nori</creatorcontrib><collection>AGRIS</collection><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>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</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>ProQuest Central China</collection><collection>Genetics Abstracts</collection><jtitle>Molecular genetics and genomics : MGG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Tadzunu</au><au>Eiguchi, Mitsugu</au><au>Kumamaru, Toshihiro</au><au>Satoh, Hikaru</au><au>Matsusaka, Hiroaki</au><au>Moriguchi, Kazuki</au><au>Nagato, Yasuo</au><au>Kurata, Nori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MNU-induced mutant pools and high performance TILLING enable finding of any gene mutation in rice</atitle><jtitle>Molecular genetics and genomics : MGG</jtitle><stitle>Mol Genet Genomics</stitle><addtitle>Mol Genet Genomics</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>279</volume><issue>3</issue><spage>213</spage><epage>223</epage><pages>213-223</pages><issn>1617-4615</issn><eissn>1617-4623</eissn><abstract>Mutant populations are indispensable genetic resources for functional genomics in all organisms. However, suitable rice mutant populations, induced either by chemicals or irradiation still have been rarely developed to date. To produce mutant pools and to launch a search system for rice gene mutations, we developed mutant populations of Oryza sativa japonica cv. Taichung 65, by treating single zygotic cells with N-methyl-N-nitrosourea (MNU). Mutagenesis in single zygotes can create mutations at a high frequency and rarely forms chimeric plants. A modified TILLING system using non-labeled primers and fast capillary gel electrophoresis was applied for high-throughput detection of single nucleotide substitution mutations. The mutation rate of an M₂ mutant population was calculated as 7.4 x 10-⁶ per nucleotide representing one mutation in every 135 kb genome sequence. One can expect 7.4 single nucleotide substitution mutations in every 1 kb of gene region when using 1,000 M₂ mutant lines. The mutations were very evenly distributed over the regions examined. These results indicate that our rice mutant population generated by MNU-mutagenesis could be a promising resource for identifying mutations in any gene of rice. The modified TILLING method also proved very efficient and convenient in screening the mutant population.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>17952471</pmid><doi>10.1007/s00438-007-0293-2</doi><tpages>11</tpages></addata></record> |
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subjects | Alleles Animal Genetics and Genomics Base Sequence Biochemistry Biomedical and Life Sciences DNA Mutational Analysis - methods DNA Primers - genetics DNA, Plant - genetics Genes Genes, Plant - drug effects Genetic Techniques Genetics Genomes Genomics Human Genetics Life Sciences Methylnitrosourea - toxicity Microbial Genetics and Genomics Mutagenesis Mutagens - toxicity Mutation Original Paper Oryza Oryza - drug effects Oryza - genetics Oryza sativa Plant Genetics and Genomics Polymerase Chain Reaction Rice Seeds |
title | MNU-induced mutant pools and high performance TILLING enable finding of any gene mutation in rice |
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