Počet záznamů: 1  

Fine Mapping of Lr49 Using 90K SNP Chip Array and Flow-Sorted Chromosome Sequencing in Wheat

  1. 1.
    SYSNO ASEP0523435
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevFine Mapping of Lr49 Using 90K SNP Chip Array and Flow-Sorted Chromosome Sequencing in Wheat
    Tvůrce(i) Nsabiyera, V. (AU)
    Baranwal, D. (AU)
    Qureshi, N. (US)
    Kay, P. (AU)
    Forrest, K. L. (AU)
    Valárik, Miroslav (UEB-Q) RID, ORCID
    Doležel, Jaroslav (UEB-Q) RID, ORCID
    Hayden, M. J. (AU)
    Bariana, H. (AU)
    Bansal, U. (AU)
    Celkový počet autorů10
    Číslo článku1787
    Zdroj.dok.Frontiers in Plant Science. - : Frontiers Research Foundation - ISSN 1664-462X
    Roč. 10, FEB 4 (2020)
    Poč.str.11 s.
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovaadult plant resistance ; chromosome sorting ; Infinium iSelect 90K SNP array ; leaf rust ; marker assisted breeding
    Vědní obor RIVEB - Genetika a molekulární biologie
    Obor OECDBiochemistry and molecular biology
    CEPEF16_019/0000827 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Způsob publikováníOpen access
    Institucionální podporaUEB-Q - RVO:61389030
    UT WOS000515758000001
    EID SCOPUS85079645049
    DOI10.3389/fpls.2019.01787
    AnotaceLeaf rust, caused by Puccinia triticina, threatens global wheat production due to the constant evolution of virulent pathotypes that defeat commercially deployed all stage-resistance (ASR) genes in modern cultivars. Hence, the deployment of combinations of adult plant resistance (APR) and ASR genes in new wheat cultivars is desirable. Adult plant resistance gene Lr49 was previously mapped on the long arm of chromosome 4B of cultivar VL404 and flanked by microsatellite markers barc163 (8.1 cM) and wmc349 (10.1 cM), neither of which was sufficiently closely linked for efficient marker assisted selection. This study used high-density SNP genotyping and flow sorted chromosome sequencing to fine-map the Lr49 locus as a starting point to develop a diagnostic marker for use in breeding and to clone this gene. Marker sunKASP_21 was mapped 0.4 cM proximal to Lr49, whereas a group of markers including sunKASP_24 were placed 0.6 cM distal to this gene. Testing of the linked markers on 75 Australian and 90 European cultivars with diverse genetic backgrounds showed that sunKASP_21 was most strongly associated with Lr49. Our results also show that the Lr49 genomic region contains structural variation relative to the reference stock Chinese Spring, possibly an inverted genomic duplication, which introduces a new set of challenges for the Lr49 cloning.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2020
    Elektronická adresahttp://doi.org/10.3389/fpls.2019.01787
Počet záznamů: 1  

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