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Registro Completo |
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Biblioteca(s): |
Embrapa Hortaliças. |
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Data corrente: |
14/02/2025 |
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Data da última atualização: |
14/02/2025 |
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Tipo da produção científica: |
Capítulo em Livro Técnico-Científico |
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Autoria: |
MORAIS, I. J.; INOUE-NAGATA, A. K.; NAKASU, E. Y. T. |
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Afiliação: |
IVAIR J. MORAIS, UNIVERSIDADE DE BRASÍLIA; ALICE KAZUKO INOUE NAGATA, CNPH; ERICH YUKIO TEMPEL NAKASU, CNPH. |
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Título: |
Construction of geminivirus infectious clones for agroinoculation into plants. |
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Ano de publicação: |
2024 |
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Fonte/Imprenta: |
In: FONTES, E. P. B.; MÄKINEN, K.(ed.). Plant-virus interactions. London: Humana Press, 2024. |
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Descrição Física: |
E-book. |
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Série: |
(Methods im molecular biology, 2724) |
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ISBN: |
978-1-0716-3485-1 |
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DOI: |
0.1007/978-1-0716-3485-1 |
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Idioma: |
Inglês |
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Conteúdo: |
The production of geminiviral infectious clones provides a standardized inoculum for use in several host–virus studies. Geminiviruses present either one (monopartite) or two (bipartite) circular single-stranded DNA components, which commonly range from 2.6 to 2.8 kb. Cloning of a monomeric genome is useful for obtaining its precise sequence. For infectious clones, however, it is essential that more than one copy of the genome, more specifically of the origin of replication, is present in order to guarantee the production of full-length progeny DNA. Here, the complete process of preparing infectious geminiviral clones is described starting from the DNA extraction and selection of restriction endonucleases followed by two protocols for constructing dimeric clones: restriction endonuclease digestion and ligation (1) and Gibson Assembly (2). |
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Palavras-Chave: |
Geminivirus. |
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Thesagro: |
Clone; Vírus. |
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Thesaurus Nal: |
Circular DNA. |
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Categoria do assunto: |
S Ciências Biológicas |
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Marc: |
LEADER 01598naa a2200241 a 4500
001 2172795
005 2025-02-14
008 2024 bl uuuu u00u1 u #d
020 $a978-1-0716-3485-1
024 7 $a0.1007/978-1-0716-3485-1$2DOI
100 1 $aMORAIS, I. J.
245 $aConstruction of geminivirus infectious clones for agroinoculation into plants.$h[electronic resource]
260 $c2024
300 $cE-book.
490 $a(Methods im molecular biology, 2724)
520 $aThe production of geminiviral infectious clones provides a standardized inoculum for use in several host–virus studies. Geminiviruses present either one (monopartite) or two (bipartite) circular single-stranded DNA components, which commonly range from 2.6 to 2.8 kb. Cloning of a monomeric genome is useful for obtaining its precise sequence. For infectious clones, however, it is essential that more than one copy of the genome, more specifically of the origin of replication, is present in order to guarantee the production of full-length progeny DNA. Here, the complete process of preparing infectious geminiviral clones is described starting from the DNA extraction and selection of restriction endonucleases followed by two protocols for constructing dimeric clones: restriction endonuclease digestion and ligation (1) and Gibson Assembly (2).
650 $aCircular DNA
650 $aClone
650 $aVírus
653 $aGeminivirus
700 1 $aINOUE-NAGATA, A. K.
700 1 $aNAKASU, E. Y. T.
773 $tIn: FONTES, E. P. B.; MÄKINEN, K.(ed.). Plant-virus interactions. London: Humana Press, 2024.
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| 1. |  | JOSHI, L. R.; MOHR, K. A.; GAVA, D.; KUTISH, G.; BUYSSE, A. S.; VANNUCCI, F. A.; PIÑEYRO, P. E.; CROSSLEY, B. M.; SCHILTZ, J. J.; JENKINS-MOORE, M.; KOSTER, L.; TELL, R.; SCHAEFER, R.; MARTHALER, D.; DIEL, D. G. Genetic diversity and evolution of the emerging picornavirus Senecavirus A. Journal of General Virology, 20 dec. 2019.| Tipo: Artigo em Periódico Indexado | Circulação/Nível: A - 1 |
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