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Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics

Rhizobia are nitrogen-fixing soil bacteria that establish endosymbiosis with some leguminous plants. The completion of several rhizobial genome sequences provides opportunities for genome-wide functional studies of the physiological roles of many rhizobial genes. In order to carry out genome-wide ph...

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Autores principales: Shimoda, Yoshikazu, Mitsui, Hisayuki, Kamimatsuse, Hiroko, Minamisawa, Kiwamu, Nishiyama, Eri, Ohtsubo, Yoshiyuki, Nagata, Yuji, Tsuda, Masataka, Shinpo, Sayaka, Watanabe, Akiko, Kohara, Mitsuyo, Yamada, Manabu, Nakamura, Yasukazu, Tabata, Satoshi, Sato, Shusei
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575893/
https://www.ncbi.nlm.nih.gov/pubmed/18658183
http://dx.doi.org/10.1093/dnares/dsn017
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author Shimoda, Yoshikazu
Mitsui, Hisayuki
Kamimatsuse, Hiroko
Minamisawa, Kiwamu
Nishiyama, Eri
Ohtsubo, Yoshiyuki
Nagata, Yuji
Tsuda, Masataka
Shinpo, Sayaka
Watanabe, Akiko
Kohara, Mitsuyo
Yamada, Manabu
Nakamura, Yasukazu
Tabata, Satoshi
Sato, Shusei
author_facet Shimoda, Yoshikazu
Mitsui, Hisayuki
Kamimatsuse, Hiroko
Minamisawa, Kiwamu
Nishiyama, Eri
Ohtsubo, Yoshiyuki
Nagata, Yuji
Tsuda, Masataka
Shinpo, Sayaka
Watanabe, Akiko
Kohara, Mitsuyo
Yamada, Manabu
Nakamura, Yasukazu
Tabata, Satoshi
Sato, Shusei
author_sort Shimoda, Yoshikazu
collection PubMed
description Rhizobia are nitrogen-fixing soil bacteria that establish endosymbiosis with some leguminous plants. The completion of several rhizobial genome sequences provides opportunities for genome-wide functional studies of the physiological roles of many rhizobial genes. In order to carry out genome-wide phenotypic screenings, we have constructed a large mutant library of the nitrogen-fixing symbiotic bacterium, Mesorhizobium loti, by transposon mutagenesis. Transposon insertion mutants were generated using the signature-tagged mutagenesis (STM) technique and a total of 29 330 independent mutants were obtained. Along with the collection of transposon mutants, we have determined the transposon insertion sites for 7892 clones, and confirmed insertions in 3680 non-redundant M. loti genes (50.5% of the total number of M. loti genes). Transposon insertions were randomly distributed throughout the M. loti genome without any bias toward G+C contents of insertion target sites and transposon plasmids used for the mutagenesis. We also show the utility of STM mutants by examining the specificity of signature tags and test screenings for growth- and nodulation-deficient mutants. This defined mutant library allows for genome-wide forward- and reverse-genetic functional studies of M. loti and will serve as an invaluable resource for researchers to further our understanding of rhizobial biology.
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spelling pubmed-25758932009-04-13 Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics Shimoda, Yoshikazu Mitsui, Hisayuki Kamimatsuse, Hiroko Minamisawa, Kiwamu Nishiyama, Eri Ohtsubo, Yoshiyuki Nagata, Yuji Tsuda, Masataka Shinpo, Sayaka Watanabe, Akiko Kohara, Mitsuyo Yamada, Manabu Nakamura, Yasukazu Tabata, Satoshi Sato, Shusei DNA Res Full Papers Rhizobia are nitrogen-fixing soil bacteria that establish endosymbiosis with some leguminous plants. The completion of several rhizobial genome sequences provides opportunities for genome-wide functional studies of the physiological roles of many rhizobial genes. In order to carry out genome-wide phenotypic screenings, we have constructed a large mutant library of the nitrogen-fixing symbiotic bacterium, Mesorhizobium loti, by transposon mutagenesis. Transposon insertion mutants were generated using the signature-tagged mutagenesis (STM) technique and a total of 29 330 independent mutants were obtained. Along with the collection of transposon mutants, we have determined the transposon insertion sites for 7892 clones, and confirmed insertions in 3680 non-redundant M. loti genes (50.5% of the total number of M. loti genes). Transposon insertions were randomly distributed throughout the M. loti genome without any bias toward G+C contents of insertion target sites and transposon plasmids used for the mutagenesis. We also show the utility of STM mutants by examining the specificity of signature tags and test screenings for growth- and nodulation-deficient mutants. This defined mutant library allows for genome-wide forward- and reverse-genetic functional studies of M. loti and will serve as an invaluable resource for researchers to further our understanding of rhizobial biology. Oxford University Press 2008-10 2008-07-25 /pmc/articles/PMC2575893/ /pubmed/18658183 http://dx.doi.org/10.1093/dnares/dsn017 Text en © The Author 2008. Kazusa DNA Research Institute
spellingShingle Full Papers
Shimoda, Yoshikazu
Mitsui, Hisayuki
Kamimatsuse, Hiroko
Minamisawa, Kiwamu
Nishiyama, Eri
Ohtsubo, Yoshiyuki
Nagata, Yuji
Tsuda, Masataka
Shinpo, Sayaka
Watanabe, Akiko
Kohara, Mitsuyo
Yamada, Manabu
Nakamura, Yasukazu
Tabata, Satoshi
Sato, Shusei
Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
title Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
title_full Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
title_fullStr Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
title_full_unstemmed Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
title_short Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
title_sort construction of signature-tagged mutant library in mesorhizobium loti as a powerful tool for functional genomics
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2575893/
https://www.ncbi.nlm.nih.gov/pubmed/18658183
http://dx.doi.org/10.1093/dnares/dsn017
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