Naslov
Saturation of Genomic Regions Conferring Broomrape and Ascochyta Blight Resistance in Faba Bean (Vicia faba L.)

Autori
Garcia, Gloria Maria ; Torres, Ana Maria ; Šatović, Zlatko ; Roman, Belen ; Moreno, Maria Teresa ; Cubero, Jose Ignacio ; Avila, Carmen

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Proceedings of the 43rd Croatian and 3rd International Symposium on Agriculture / Pospišil, Milan - Zagreb : Agronomski fakultet Sveučilišta u Zagrebu, 2008, 92-93

ISBN
978-953-6135-68-4

Skup
43rd Croatian and 3rd International Symposium on Agriculture

Mjesto i datum
Opatija, Hrvatska, 18.02.2008. - 21.02.2008

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Faba bean; Resistance breeding; Quantiative trait loci (QTLs); Bulk segregant analysis (BSA); Saturation mapping

Sažetak
Broomrape (Orobanche crenata Forsk.) and ascochyta blight (caused by Ascochyta fabae Speg.) resistance in faba bean (Vicia faba L.) are complex traits, difficult to manipulate using conventional breeding procedures. The accurate identification of genomic locations of individual quantitative trait loci (QTLs) controlling resistance is of utmost importance in order to develop marker-assisted selection (MAS) programmes. Previous QTL mapping studies in F2 as well as in recombinant inbred lines (RIL) population detected two QTLs controlling broomrape resistance that were stable across generations and across environments: Oc2 (linkage group VI.B) and Oc3 (LG II.A). Similarly, two QTLs conferring resistance to Ascochyta fabae were identified in F2 population and further validated in RILs: Af1 (LG III.A) and Af2 (LG II.A). Bulked segregant analysis (BSA) based on previous QTL mapping information was applied to saturate the targeted regions. Bulks fixed for alleles of the two markers flanking four QTL regions were selected from the RIL population. More than seven hundred RAPD primers were screened for polymorphism between the two bulks of each target region revealing 31 putatively linked markers. Twenty-four out of 31 RAPD markers were mapped to target linkage groups: 11 to LG VI.B (Oc2), 8 to LG II.A (Oc3 and Af2), and 5 to LG III.A (Af1). By inclusion of additional markers the average intermarker distance on target linkage groups significantly decreased allowing more accurate determination of QTL locations and effects.

Izvorni jezik
Engleski

Znanstvena područja
Poljoprivreda (agronomija), Biotehnologija

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