Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray

A cassava cDNA microarray based on a large cassava EST database was constructed and used to study the incompatible interaction between cassava and Xanthomonas axonopodis pv. manihotis (Xam) strain CIO151. For microarray construction, 5700 clones from the cassava unigene set were amplified by polymer...

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Autores principales: López, C.E., Soto Suárez, M., Restrepo, S., Piegu, B, Cooke, R.G., Delseny, M, Tohme, Joseph M., Verdier, Valerie M.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Springer 2005
Materias:
Acceso en línea:https://hdl.handle.net/10568/42876
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author López, C.E.
Soto Suárez, M.
Restrepo, S.
Piegu, B
Cooke, R.G.
Delseny, M
Tohme, Joseph M.
Verdier, Valerie M.
author_browse Cooke, R.G.
Delseny, M
López, C.E.
Piegu, B
Restrepo, S.
Soto Suárez, M.
Tohme, Joseph M.
Verdier, Valerie M.
author_facet López, C.E.
Soto Suárez, M.
Restrepo, S.
Piegu, B
Cooke, R.G.
Delseny, M
Tohme, Joseph M.
Verdier, Valerie M.
author_sort López, C.E.
collection Repository of Agricultural Research Outputs (CGSpace)
description A cassava cDNA microarray based on a large cassava EST database was constructed and used to study the incompatible interaction between cassava and Xanthomonas axonopodis pv. manihotis (Xam) strain CIO151. For microarray construction, 5700 clones from the cassava unigene set were amplified by polymerase chain reaction (PCR) and printed on glass slides. Microarray hybridization was performed using cDNA from cassava plants (resistant variety MBra685) collected at 12, 24, 48 h and 7 and 15 days post-infection as treatment and cDNA from mock-inoculated plants as control. A total of 199 genes were found to be differentially expressed (126 up-regulated and 73 down-regulated). A greater proportion of differentially-expressed genes was observed at 7 days after inoculation. Expression profiling and cluster analyses indicate that, in response to inoculation with Xam, cassava induces dozens of genes, including principally those involved in oxidative burst, protein degradation and pathogenesis-related (PR) genes. In contrast, genes encoding proteins that are involved in photosynthesis and metabolism were down regulated. In addition, various other genes encoding proteins with unknown function or showing no similarity to other proteins were also induced. Quantitative real time PCR experiments confirmed the reliability of our microarray data. In addition we showed that some genes are induced more rapidly in the resistant than in the susceptible cultivar.
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spelling CGSpace428762024-08-27T10:37:08Z Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray López, C.E. Soto Suárez, M. Restrepo, S. Piegu, B Cooke, R.G. Delseny, M Tohme, Joseph M. Verdier, Valerie M. manihot esculenta xanthomonas axonopodis gene expression genetic resistance genetic markers expresión génica resistencia genética marcadores genéticos A cassava cDNA microarray based on a large cassava EST database was constructed and used to study the incompatible interaction between cassava and Xanthomonas axonopodis pv. manihotis (Xam) strain CIO151. For microarray construction, 5700 clones from the cassava unigene set were amplified by polymerase chain reaction (PCR) and printed on glass slides. Microarray hybridization was performed using cDNA from cassava plants (resistant variety MBra685) collected at 12, 24, 48 h and 7 and 15 days post-infection as treatment and cDNA from mock-inoculated plants as control. A total of 199 genes were found to be differentially expressed (126 up-regulated and 73 down-regulated). A greater proportion of differentially-expressed genes was observed at 7 days after inoculation. Expression profiling and cluster analyses indicate that, in response to inoculation with Xam, cassava induces dozens of genes, including principally those involved in oxidative burst, protein degradation and pathogenesis-related (PR) genes. In contrast, genes encoding proteins that are involved in photosynthesis and metabolism were down regulated. In addition, various other genes encoding proteins with unknown function or showing no similarity to other proteins were also induced. Quantitative real time PCR experiments confirmed the reliability of our microarray data. In addition we showed that some genes are induced more rapidly in the resistant than in the susceptible cultivar. 2005-02 2014-09-24T07:58:42Z 2014-09-24T07:58:42Z Journal Article https://hdl.handle.net/10568/42876 en Limited Access Springer
spellingShingle manihot esculenta
xanthomonas axonopodis
gene expression
genetic resistance
genetic markers
expresión génica
resistencia genética
marcadores genéticos
López, C.E.
Soto Suárez, M.
Restrepo, S.
Piegu, B
Cooke, R.G.
Delseny, M
Tohme, Joseph M.
Verdier, Valerie M.
Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray
title Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray
title_full Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray
title_fullStr Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray
title_full_unstemmed Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray
title_short Gene expression profile in response to Xanthomonas axonopodis pv. manihotis infection in cassava using a cDNA microarray
title_sort gene expression profile in response to xanthomonas axonopodis pv manihotis infection in cassava using a cdna microarray
topic manihot esculenta
xanthomonas axonopodis
gene expression
genetic resistance
genetic markers
expresión génica
resistencia genética
marcadores genéticos
url https://hdl.handle.net/10568/42876
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