Articles
DEVELOPMENT OF MOLECULAR MARKERS LINKED TO THE TRAITS OF NON-ACID/ ACID FRUIT OF PEACH
Article number
763_17
Pages
131 – 138
Language
English
Abstract
AFLP and bulked segregant analysis were used to screen markers linked to the non-acid/acid trait of peach fruit controlled by D/d gene.
Of 64 pairs of primer combinations, twelve amplified polymorphic DNA fragments between non-acid bulk and acid bulk.
Only two specific fragments were linked to acid trait (recessive d location), after investigating the progenies.
Specific fragments TA-CTC140 and AT-CTA200 were derived from primers E-TA/M-CTC and E-AT/M-CTA. The linkage distances to D/d gene were 1.47cM and 2.99cM, respectively.
Specific primers BFPA1/A2 and BFPB1/B2 were designed according to the sequences of two specific fragments.
With primers BFPB1/B2, genomic DNA amplified the polymorphic band AT-CTA158 in acid bulks and individuals.
The AFLP marker AT-CTA200 was converted into a SCAR marker.
The linkage distance of marker AT-CTA158 to d gene was the same as that of the original AFLP marker.
However, the AFLP marker TA-CTC140 was not converted into a SCAR marker.
Polymorphism disappeared in both parents and progenies when amplified with primer pair A1/A2.
Of 64 pairs of primer combinations, twelve amplified polymorphic DNA fragments between non-acid bulk and acid bulk.
Only two specific fragments were linked to acid trait (recessive d location), after investigating the progenies.
Specific fragments TA-CTC140 and AT-CTA200 were derived from primers E-TA/M-CTC and E-AT/M-CTA. The linkage distances to D/d gene were 1.47cM and 2.99cM, respectively.
Specific primers BFPA1/A2 and BFPB1/B2 were designed according to the sequences of two specific fragments.
With primers BFPB1/B2, genomic DNA amplified the polymorphic band AT-CTA158 in acid bulks and individuals.
The AFLP marker AT-CTA200 was converted into a SCAR marker.
The linkage distance of marker AT-CTA158 to d gene was the same as that of the original AFLP marker.
However, the AFLP marker TA-CTC140 was not converted into a SCAR marker.
Polymorphism disappeared in both parents and progenies when amplified with primer pair A1/A2.
Authors
Jun Wu, Huairui Shu, Kaichun Zhang, Lijie Jiang
Keywords
Prunus persica (L.) Batsch, AFLP, SCAR
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