Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1124870
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dc.contributor.authorGODDARD, R.
dc.contributor.authorSTEED, A.
dc.contributor.authorCHINOY, C.
dc.contributor.authorFERREIRA, J. R.
dc.contributor.authorSCHEEREN, P. L.
dc.contributor.authorMACIEL, J. L. N.
dc.contributor.authorCAIERAO, E.
dc.contributor.authorTORRES, G. A. M.
dc.contributor.authorCONSOLI, L.
dc.contributor.authorSANTANA, F. M.
dc.contributor.authorFERNANDES, J. M. C.
dc.contributor.authorSIMMONDS, J.
dc.contributor.authorUAUY, C.
dc.contributor.authorCOCKRAM, J.
dc.contributor.authorNICHOLSON, P.
dc.date.accessioned2020-09-11T17:14:54Z-
dc.date.available2020-09-11T17:14:54Z-
dc.date.created2020-09-11
dc.date.issued2020
dc.identifier.citationBMC Plant Biology, v. 20, n. 398, Aug. 2020.
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1124870-
dc.descriptionBackground: Wheat blast, caused by Magnaporthe oryzae Triticum (MoT) pathotype, is a global threat to wheat (Triticum aestivum L.) production. Few blast resistance (R) genes have been identified to date, therefore assessing potential sources of resistance in wheat is important. The Brazilian wheat cultivar BR 18-Terena is considered one of the best sources of resistance to blast and has been widely used in Brazilian breeding programmes, however the underlying genetics of this resistance are unknown. Results: BR 18-Terena was used as the common parent in the development of two recombinant inbred line (RIL) F6 populations with the Brazilian cultivars Anahuac 75 and BRS 179. Populations were phenotyped for resistance at the seedling and heading stage using the sequenced MoT isolate BR32, with transgressive segregation being observed. Genetic maps containing 1779 and 1318 markers, were produced for the Anahuac 75 × BR 18-Terena and BR 18- Terena × BRS 179 populations, respectively. Five quantitative trait loci (QTL) associated with seedling resistance, on chromosomes 2B, 4B (2 QTL), 5A and 6A, were identified, as were four QTL associated with heading stage resistance (1A, 2B, 4A and 5A). Seedling and heading stage QTL did not co-locate, despite a significant positive correlation between these traits, indicating that resistance at these developmental stages is likely to be controlled by different genes. BR 18-Terena provided the resistant allele for six QTL, at both developmental stages, with the largest phenotypic effect conferred by a QTL being 24.8% suggesting that BR 18-Terena possesses quantitative resistance. Haplotype analysis of 100 Brazilian wheat cultivars indicates that 11.0% of cultivars already possess a BR 18-Terenalike haplotype for more than one of the identified heading stage QTL. Conclusions: This study suggests that BR 18-Terena possesses quantitative resistance to wheat blast, with nine QTL associated with resistance at either the seedling or heading stage being detected. Wheat blast resistance is also largely tissue-specific. Identification of durable quantitative resistances which can be combined with race-specific R gene-mediated resistance is critical to effectively control wheat blast. Collectively, this work facilitates markerassisted selection to develop new varieties for cultivation in regions at risk from this emerging disease.
dc.language.isoeng
dc.rightsopenAccesseng
dc.subjectWheat blast
dc.subjectSeedling resistance
dc.subjectHead resistance
dc.subjectSingle nucleotide polymorphism (SNP) genotyping
dc.titleDissecting the genetic basis of wheat blast resistance in the Brazilian wheat cultivar BR 18-Terena.
dc.typeArtigo de periódico
dc.subject.thesagroTriticum Aestivum
dc.subject.nalthesaurusMagnaporthe oryzae
dc.subject.nalthesaurusQuantitative trait loci
dc.subject.nalthesaurusGenotyping
riaa.ainfo.id1124870
riaa.ainfo.lastupdate2021-02-25 -03:00
dc.identifier.doihttps://doi.org/10.1186/s12870-020-02592-0
dc.contributor.institutionRACHEL R. GODDARD, Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, UK
dc.contributor.institutionANDREW STEED, Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, UKeng
dc.contributor.institutionCATHERINE CHINOY, Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, UKeng
dc.contributor.institutionJÉSSICA ROSSET FERREIRA, Universidade de Passo Fundo, Passo Fundo, RS, Brazileng
dc.contributor.institutionPEDRO LUIZ SCHEEREN, CNPTeng
dc.contributor.institutionJOAO LEODATO NUNES MACIEL, CNPTeng
dc.contributor.institutionEDUARDO CAIERAO, CNPTeng
dc.contributor.institutionGISELE ABIGAIL MONTAN TORRES, CNPTeng
dc.contributor.institutionLUCIANO CONSOLI, CNPTeng
dc.contributor.institutionFLAVIO MARTINS SANTANA, CNPTeng
dc.contributor.institutionJOSE MAURICIO CUNHA FERNANDES, CNPTeng
dc.contributor.institutionJames Simmonds, Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, UKeng
dc.contributor.institutionCRISTOBAL UAUY, Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, UKeng
dc.contributor.institutionJames Cockram, John Bingham Laboratory, NIAB, Cambridge, UKeng
dc.contributor.institutionPaul Nicholson, Department of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich, UK.eng
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