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dc.contributorFacultad de Ciencias Biologicas y Ambientaleses_ES
dc.contributor.authorPolanco de la Puente, Carlos Gaspar 
dc.contributor.authorSáenz de Miera Carnicer, Luis Enrique 
dc.contributor.authorBett, Kirstin
dc.contributor.authorPérez de la Vega, Marcelino 
dc.contributor.otherGeneticaes_ES
dc.date2018
dc.date.accessioned2019-10-04T09:11:33Z
dc.date.available2019-10-04T09:11:33Z
dc.identifier.citationPLoS ONE 13(3): e0194945.es_ES
dc.identifier.otherhttps://doi.org/10.1371/journal.pone.0194945es_ES
dc.identifier.urihttp://hdl.handle.net/10612/11116
dc.descriptionRevista electrónica on linees_ES
dc.description.abstractPowdery mildew is a widespread fungal plant disease that can cause significant losses in many crops. Some MLO genes (Mildew resistance locus O) have proved to confer a durable resistance to powdery mildew in several species. Resistance granted by the MLO gene family members has prompted an increasing interest in characterizing these genes and implementing their use in plant breeding. Lentil (Lens culinaris Medik.) is a widely grown food legume almost exclusively consumed as dry seed with an average world production of 4.5 million tons. Powdery mildew causes severe losses on certain lentil cultivars under particular environmental conditions. Data mining of the lentil CDC Redberry draft genome allowed to identify up to 15 gene sequences with homology to known MLO genes, designated as LcMLOs. Further characterization of these gene sequences and their deduced protein sequences demonstrated conformity with key MLO protein characteristics such as the presence of transmembrane and calmodulin binding domains, as well as that of other conserved motifs. Phylogenetic and other comparative analyses revealed that LcMLO1 and LcMLO3 are the most likely gene orthologs related to powdery mildew response in other species, sharing a high similarity with other known resistance genes of dicot species, such as pea PsMLO1 and Medicago truncatula MtMLO1 and MtMLO3. Sets of primers were designed as tools to PCR amplify the genomic sequences of LcMLO1 and LcMLO3, also to screen lentil germplasm in search of resistance mutants. Primers were used to obtain the complete sequences of these two genes in all of the six wild lentil relatives. Respective to each gene, all Lens sequences shared a high similarity. Likewise, we used these primers to screen a working collection of 58 cultivated and 23 wild lentil accessions in search of length polymorphisms present in these two genes. All these data widen the insights on this gene family and can be useful for breeding programs in lentil and close related species.es_ES
dc.languageenges_ES
dc.publisherPLoSes_ES
dc.subjectGenéticaes_ES
dc.subject.otherGenomaes_ES
dc.titleA genome-wide identification and comparative analysis of the lentil MLO geneses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1371/journal.pone.0194945
dc.description.peerreviewedSIes_ES
dc.relation.projectIDAGL2013- 44714-R, FP7 613551 (LEGumes for the Agriculture of Tomorrow; LEGATO), Junta de Castilla y León (GR113)es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1932-6203
dc.journal.titlePLOS ONEes_ES
dc.volume.number13es_ES
dc.issue.number3es_ES
dc.type.hasVersioninfo:eu-repo/semantics/draftes_ES
dc.subject.unesco2409 Genéticaes_ES


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