Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress
- Autores
- Ulrich, Maria Noelia; Muñiz Padilla, Esteban Tobias; Corach, Alejandra; Hopp, Horacio Esteban; Tosto, Daniela Sandra
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Weeds are one of the main causes of the decrease in crop yields, with Johnsongrass (Sorghum halepense L.) being one of the most significant. Weeds can be controlled by herbicides, but some have developed resistance. Quantitative PCR is the technique of choice for studying gene expression related to herbicide resistance because of its high sensitivity and specificity, although its quantitative accuracy is highly dependent on the stability of the reference genes. Thus, in this study we evaluated the stability of different reference genes of glyphosate-resistant S. halepense. Nine genes frequently used as reference genes were selected: MDH, ADP, PP2A, EIF4α, ACT, ARI8, DnaJ, Hsp70, and ALS1, and their expression analyzed in susceptible and resistant biotypes at 0, 24 and 72 h post-application of glyphosate. The stability was analyzed with the geNorm, NormFinder, and BestKeeper software programs and using the ∆Ct method. RefFinder was used to generate a comprehensive stability ranking. The results showed that PP2A and ARI8 were the most stable genes under the test conditions. EPSPS expression was also verified against the best two and the worst two reference genes. This study provides useful information for gene expression analysis under glyphosate stress and will facilitate resistance mechanism studies in this weed species.
Fil: Ulrich, Maria Noelia. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Agrobiotecnología y Biología Molecular. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Agrobiotecnología y Biología Molecular; Argentina
Fil: Muñiz Padilla, Esteban Tobias. Universidad Nacional de Entre Ríos; Argentina
Fil: Corach, Alejandra. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Agrobiotecnología y Biología Molecular. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Agrobiotecnología y Biología Molecular; Argentina
Fil: Hopp, Horacio Esteban. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires; Argentina
Fil: Tosto, Daniela Sandra. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina - Materia
-
GENE EXPRESSION
HERBICIDE RESISTANCE
RT-QPCR
WEEDS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/182276
Ver los metadatos del registro completo
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Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stressUlrich, Maria NoeliaMuñiz Padilla, Esteban TobiasCorach, AlejandraHopp, Horacio EstebanTosto, Daniela SandraGENE EXPRESSIONHERBICIDE RESISTANCERT-QPCRWEEDShttps://purl.org/becyt/ford/4.5https://purl.org/becyt/ford/4Weeds are one of the main causes of the decrease in crop yields, with Johnsongrass (Sorghum halepense L.) being one of the most significant. Weeds can be controlled by herbicides, but some have developed resistance. Quantitative PCR is the technique of choice for studying gene expression related to herbicide resistance because of its high sensitivity and specificity, although its quantitative accuracy is highly dependent on the stability of the reference genes. Thus, in this study we evaluated the stability of different reference genes of glyphosate-resistant S. halepense. Nine genes frequently used as reference genes were selected: MDH, ADP, PP2A, EIF4α, ACT, ARI8, DnaJ, Hsp70, and ALS1, and their expression analyzed in susceptible and resistant biotypes at 0, 24 and 72 h post-application of glyphosate. The stability was analyzed with the geNorm, NormFinder, and BestKeeper software programs and using the ∆Ct method. RefFinder was used to generate a comprehensive stability ranking. The results showed that PP2A and ARI8 were the most stable genes under the test conditions. EPSPS expression was also verified against the best two and the worst two reference genes. This study provides useful information for gene expression analysis under glyphosate stress and will facilitate resistance mechanism studies in this weed species.Fil: Ulrich, Maria Noelia. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Agrobiotecnología y Biología Molecular. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Agrobiotecnología y Biología Molecular; ArgentinaFil: Muñiz Padilla, Esteban Tobias. Universidad Nacional de Entre Ríos; ArgentinaFil: Corach, Alejandra. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Agrobiotecnología y Biología Molecular. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Agrobiotecnología y Biología Molecular; ArgentinaFil: Hopp, Horacio Esteban. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires; ArgentinaFil: Tosto, Daniela Sandra. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaMultidisciplinary Digital Publishing Institute2021-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/182276Ulrich, Maria Noelia; Muñiz Padilla, Esteban Tobias; Corach, Alejandra; Hopp, Horacio Esteban; Tosto, Daniela Sandra; Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress; Multidisciplinary Digital Publishing Institute; Plants; 10; 8; 8-2021; 1-132223-7747CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.3390/plants10081555info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2223-7747/10/8/1555info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:40:41Zoai:ri.conicet.gov.ar:11336/182276instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:40:41.708CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
title |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
spellingShingle |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress Ulrich, Maria Noelia GENE EXPRESSION HERBICIDE RESISTANCE RT-QPCR WEEDS |
title_short |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
title_full |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
title_fullStr |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
title_full_unstemmed |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
title_sort |
Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress |
dc.creator.none.fl_str_mv |
Ulrich, Maria Noelia Muñiz Padilla, Esteban Tobias Corach, Alejandra Hopp, Horacio Esteban Tosto, Daniela Sandra |
author |
Ulrich, Maria Noelia |
author_facet |
Ulrich, Maria Noelia Muñiz Padilla, Esteban Tobias Corach, Alejandra Hopp, Horacio Esteban Tosto, Daniela Sandra |
author_role |
author |
author2 |
Muñiz Padilla, Esteban Tobias Corach, Alejandra Hopp, Horacio Esteban Tosto, Daniela Sandra |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
GENE EXPRESSION HERBICIDE RESISTANCE RT-QPCR WEEDS |
topic |
GENE EXPRESSION HERBICIDE RESISTANCE RT-QPCR WEEDS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/4.5 https://purl.org/becyt/ford/4 |
dc.description.none.fl_txt_mv |
Weeds are one of the main causes of the decrease in crop yields, with Johnsongrass (Sorghum halepense L.) being one of the most significant. Weeds can be controlled by herbicides, but some have developed resistance. Quantitative PCR is the technique of choice for studying gene expression related to herbicide resistance because of its high sensitivity and specificity, although its quantitative accuracy is highly dependent on the stability of the reference genes. Thus, in this study we evaluated the stability of different reference genes of glyphosate-resistant S. halepense. Nine genes frequently used as reference genes were selected: MDH, ADP, PP2A, EIF4α, ACT, ARI8, DnaJ, Hsp70, and ALS1, and their expression analyzed in susceptible and resistant biotypes at 0, 24 and 72 h post-application of glyphosate. The stability was analyzed with the geNorm, NormFinder, and BestKeeper software programs and using the ∆Ct method. RefFinder was used to generate a comprehensive stability ranking. The results showed that PP2A and ARI8 were the most stable genes under the test conditions. EPSPS expression was also verified against the best two and the worst two reference genes. This study provides useful information for gene expression analysis under glyphosate stress and will facilitate resistance mechanism studies in this weed species. Fil: Ulrich, Maria Noelia. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Agrobiotecnología y Biología Molecular. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Agrobiotecnología y Biología Molecular; Argentina Fil: Muñiz Padilla, Esteban Tobias. Universidad Nacional de Entre Ríos; Argentina Fil: Corach, Alejandra. Instituto Nacional de Tecnología Agropecuaria. Centro de Investigación en Ciencias Veterinarias y Agronómicas. Instituto de Agrobiotecnología y Biología Molecular. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Agrobiotecnología y Biología Molecular; Argentina Fil: Hopp, Horacio Esteban. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires; Argentina Fil: Tosto, Daniela Sandra. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina |
description |
Weeds are one of the main causes of the decrease in crop yields, with Johnsongrass (Sorghum halepense L.) being one of the most significant. Weeds can be controlled by herbicides, but some have developed resistance. Quantitative PCR is the technique of choice for studying gene expression related to herbicide resistance because of its high sensitivity and specificity, although its quantitative accuracy is highly dependent on the stability of the reference genes. Thus, in this study we evaluated the stability of different reference genes of glyphosate-resistant S. halepense. Nine genes frequently used as reference genes were selected: MDH, ADP, PP2A, EIF4α, ACT, ARI8, DnaJ, Hsp70, and ALS1, and their expression analyzed in susceptible and resistant biotypes at 0, 24 and 72 h post-application of glyphosate. The stability was analyzed with the geNorm, NormFinder, and BestKeeper software programs and using the ∆Ct method. RefFinder was used to generate a comprehensive stability ranking. The results showed that PP2A and ARI8 were the most stable genes under the test conditions. EPSPS expression was also verified against the best two and the worst two reference genes. This study provides useful information for gene expression analysis under glyphosate stress and will facilitate resistance mechanism studies in this weed species. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-08 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/182276 Ulrich, Maria Noelia; Muñiz Padilla, Esteban Tobias; Corach, Alejandra; Hopp, Horacio Esteban; Tosto, Daniela Sandra; Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress; Multidisciplinary Digital Publishing Institute; Plants; 10; 8; 8-2021; 1-13 2223-7747 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/182276 |
identifier_str_mv |
Ulrich, Maria Noelia; Muñiz Padilla, Esteban Tobias; Corach, Alejandra; Hopp, Horacio Esteban; Tosto, Daniela Sandra; Validation of reference genes for quantitative pcr in johnsongrass (Sorghum halepense l.) under glyphosate stress; Multidisciplinary Digital Publishing Institute; Plants; 10; 8; 8-2021; 1-13 2223-7747 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.3390/plants10081555 info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2223-7747/10/8/1555 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute |
publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844614435916742656 |
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13.070432 |