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Registro Completo |
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
01/12/1992 |
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Data da última atualização: |
01/12/1992 |
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Autoria: |
MESHI, T.; WATANABE, Y.; SAITO, T.; SUGIMOTO, A.; MAEDA, T.; OKADA, Y. |
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Afiliação: |
Faculty of Science, University of Tokyo, Hongo, Tokyo 113, Japan. |
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Título: |
Function of the 30 kd protein of tobacco mosaic virus: involvement in cell-to-cell movement and dispensability for replication. |
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Ano de publicação: |
1987 |
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Fonte/Imprenta: |
The Embo Journal, v.6, n.9, p.2557-2563, 1987. |
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Idioma: |
Inglês |
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Conteúdo: |
We have investigated the function of the 30 kd protein of tobacco mosaic virus (TMV) by a reserve genetics approach. First, a point mutation of TMV Ls1 (a temperature-sensitive mutant defective in cell-to-cell movement), that causes an amino acid substitution in the 30 kd protein, was introduced into the parent strain, TMV L. The generated mutant showed the same phenotype as TMV Ls1, and therefore the one-base substitution in the 30 kd protein gene adequately explains the defectiveness of TMV Ls1. Next, four kinds of frame-shift mutants were constructed, whose mutations are located at three different positions of the 30 kd protein gene. All the frame-shift mutants were replication-competent in protoplasts but none showed infectivity on tobacco plants. From these observations the 30 kd protein was confirmed to be involved in cell-to-cell movement. To clarify that the 30 kd protein is not necessary for replication, two kinds of deletion mutants were construted; one lacking most of the 30 kd protein gene and the other lacking both the 30 kd and coat protein genes. Both mutants replicated in protoplasts and the former still produced the subgenomic mRNA for the coat protein. These results clearly showed that the 30 kd protein, as well as the coat protein, is dispensable for replication and thar no cisacting element for replication is located in their coding sequences. It is also suggested that the signal for coat protein mRNA synthesis may be located within about 100 nucleotides upstream of the initiation codon of the c MenosWe have investigated the function of the 30 kd protein of tobacco mosaic virus (TMV) by a reserve genetics approach. First, a point mutation of TMV Ls1 (a temperature-sensitive mutant defective in cell-to-cell movement), that causes an amino acid substitution in the 30 kd protein, was introduced into the parent strain, TMV L. The generated mutant showed the same phenotype as TMV Ls1, and therefore the one-base substitution in the 30 kd protein gene adequately explains the defectiveness of TMV Ls1. Next, four kinds of frame-shift mutants were constructed, whose mutations are located at three different positions of the 30 kd protein gene. All the frame-shift mutants were replication-competent in protoplasts but none showed infectivity on tobacco plants. From these observations the 30 kd protein was confirmed to be involved in cell-to-cell movement. To clarify that the 30 kd protein is not necessary for replication, two kinds of deletion mutants were construted; one lacking most of the 30 kd protein gene and the other lacking both the 30 kd and coat protein genes. Both mutants replicated in protoplasts and the former still produced the subgenomic mRNA for the coat protein. These results clearly showed that the 30 kd protein, as well as the coat protein, is dispensable for replication and thar no cisacting element for replication is located in their coding sequences. It is also suggested that the signal for coat protein mRNA synthesis may be located within about 100 nucleotides ... Mostrar Tudo |
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Palavras-Chave: |
30k protein; 30k proteina; Efeito; Transport effect. |
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Thesagro: |
Transporte; Vírus. |
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Categoria do assunto: |
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Marc: |
LEADER 02232naa a2200253 a 4500
001 1457955
005 1992-12-01
008 1987 bl --- 0-- u #d
100 1 $aMESHI, T.
245 $aFunction of the 30 kd protein of tobacco mosaic virus$binvolvement in cell-to-cell movement and dispensability for replication.
260 $c1987
520 $aWe have investigated the function of the 30 kd protein of tobacco mosaic virus (TMV) by a reserve genetics approach. First, a point mutation of TMV Ls1 (a temperature-sensitive mutant defective in cell-to-cell movement), that causes an amino acid substitution in the 30 kd protein, was introduced into the parent strain, TMV L. The generated mutant showed the same phenotype as TMV Ls1, and therefore the one-base substitution in the 30 kd protein gene adequately explains the defectiveness of TMV Ls1. Next, four kinds of frame-shift mutants were constructed, whose mutations are located at three different positions of the 30 kd protein gene. All the frame-shift mutants were replication-competent in protoplasts but none showed infectivity on tobacco plants. From these observations the 30 kd protein was confirmed to be involved in cell-to-cell movement. To clarify that the 30 kd protein is not necessary for replication, two kinds of deletion mutants were construted; one lacking most of the 30 kd protein gene and the other lacking both the 30 kd and coat protein genes. Both mutants replicated in protoplasts and the former still produced the subgenomic mRNA for the coat protein. These results clearly showed that the 30 kd protein, as well as the coat protein, is dispensable for replication and thar no cisacting element for replication is located in their coding sequences. It is also suggested that the signal for coat protein mRNA synthesis may be located within about 100 nucleotides upstream of the initiation codon of the c
650 $aTransporte
650 $aVírus
653 $a30k protein
653 $a30k proteina
653 $aEfeito
653 $aTransport effect
700 1 $aWATANABE, Y.
700 1 $aSAITO, T.
700 1 $aSUGIMOTO, A.
700 1 $aMAEDA, T.
700 1 $aOKADA, Y.
773 $tThe Embo Journal$gv.6, n.9, p.2557-2563, 1987.
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| 1. |  | CAMARGO, A. C. de; NOVAES, N. J.; NOVO, A. L. M.; MENDONCA, F. C.; MANZANO, A.; ESTEVES, S. N.; PAGANI NETO, C.; QIUINAGLIA NETO, P.; DIAS, A. T. F. F.; SANTOS JUNIOR, H. A. dos; RIBEIRO, W. M.; FARIA, V. P. de. Projeto Balde Cheio: transferência de tecnologia na produção leiteira - estudo de caso do sítio Boa Vista, de Elisário, SP. São Carlos, SP: Embrapa Pecuária Sudeste, 2006. 8 p. (Embrapa Pecuária Sudeste. Comunicado técnico, 71).| Tipo: Comunicado Técnico/Recomendações Técnicas |
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| 2. | | FREITAS, A. W. de P.; BERNARDI, A. C. de C.; GRASSI, A. M.; SANTOS, A. dos; GURGEL, A. C.; COSTA, A. C. P. B.; ABREU JUNIOR, A. C. de; BILLI, A. L.; SOUZA, B. F. de; PAGANI NETO, C.; CRUSCIOL, C. A. C.; CERRI, C. E. P.; MANZATTO, C. V.; DOURADO NETO, D.; ASSAD, E. D.; RIBEIRO, E. G.; PENTEADO, F. A. P. de O.; BATOLLA JUNIOR, F.; ROCHA, F. M.; OLIVEIRA, F. M. S. de; CORREA, F. A.; MATTURRO, F.; OGAWA, G.; MATEUS, G. P.; LEITE, I.; PIMENTEL, J. C. de C.; ALVES, J. W. S.; CORA, J. E.; FONTES, J. L.; MACHADO FILHO, J. V.; SKORUPA, L. A.; PREMAZZI, L. M.; SCHMIDT, L. A.; CANTO, M. S. do; CECCON, M. A. P.; FANUCCHI, M.; DRUGOWICH, M. I.; NOMURA, M. S.; LUCON, O. dos S.; OLIVEIRA, P. P. A.; HERMANN, P.; OLIVEIRA JUNIOR, P. R. de; ACUNHA, R. B.; SANTOS, R. dos; MARGATHO, S. M. F.; FRANCA, T. J. F. Plano estadual de mitigação e de adaptação às mudanças climáticas para a consolidação de uma economia de baixa emissão de carbono na agricultura. São Paulo: Ministério da Agricultura, Pecuária e Abastecimento (MAPA); Secretaria de Agricultura e Abastecimento, 2016. 56 p. Apostila| Tipo: Autoria/Organização/Edição de Livros |
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