PAG-IV Plant Genome IV Conference

Town & Country Conference Center, San Diego, CA, January, 1995.


W2
Identification of AFLP-Markers Tightly Linked to the Locus Conferring Resistance to Melampsora larici-populina in Populus

MARIA-TERESA CERVERA, Jaqueline Gusmao, Marijke Steenackers, Veronique Storme, An Vanden Broeck, Marc Van Montagu and Wout Boerjan
Laboratorium voor Genetika, University of Ghent, Ledeganckstraat 35, B9000 Ghent, Belgium

Different molecular techniques, such as restriction fragment length polymorphism (RFLP) as well as polymerase chain reaction (PCR)-based techniques, have been used with the aim of detecting molecular markers associated with qualitative or quantitative trait loci (QTL) of poplar. Special interest has been devoted to those related to disease resistance among commercially important traits. The efficiency of the indirect selection depends on the easiness of detection and the degree of linkage to the resistance locus. Several high-volume marker technologies have recently been developed. The selective restriction fragment amplification (SRFA) technique is considered to be one of the most powerful. This method, developed at Keygene by M. Zabeau and P. Vos, is used to detect amplified fragment length polymorphisms (AFLPsR). We decided to use the combination of SRFA technique and bulked segregant analysis (BSA) as an strategy to screen rapidly thousands of loci and facilitate the detection of those adjacent to the locus conferring the resistance to Melampsora larici-populina (Mr), the most common rust in Europe, in Populus. Three different genetic AFLP markers tightly linked to the Mr gene were identified in a hybrid F2 generation derived from a inter-specific controlled cross between a resistant Populus deltoides female and a susceptible P. nigra male. Linkage between those markers and the Mr dominant locus was less than 0.8, 2.4 and 0.8 cM respectively.
This work was supported by a grant from the Flemish Government (BNO/BB/6/1994) and the EEC AIR program (AIR1-CT92-0349).


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