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a New Zealand Institute for Crop & Food Research Ltd., Private Bag 4704, Christchurch, New Zealand
b Plant Sciences Group, P.O. Box 84, Lincoln Univ., Canterbury, New Zealand
c Joint Nature Conservation Committee, Monkstone House, City Road, Peterborough PE1 1JY, UK
d Dep. of Biology, Univ. of Washington, Seattle, WA 98195-1800
e Plant Research (NZ) Ltd., PO Box 19, Lincoln, New Zealand
* Corresponding author (timmermang{at}crop.cri.nz)
Seed yield in pea (Pisum sativum L.) is a physiologically complex trait that is strongly influenced by both genotype and environment. Seed yield can be described in terms of its components, which include plant number per unit area, seed weight, and seed number. These yield components show interdependence and plasticity in response to environment; therefore, selection based on a single component is unlikely to succeed in increasing yield in breeding programs. To improve our understanding of the genetic basis of seed yield determination in pea and to identify genetic loci involved, quantitative trait loci (QTL) for yield per se, yield components (seed weight, seed number, and harvest index [HI]) and developmental traits (node of first flower [NFF], number of flowering nodes [NFN], total node number [TNN]) were mapped. The QTL mapping was conducted using F2derived families of a cross between Primo, a marrowfat cultivar, and OSU442-15, a blue pea breeding line. Linkage maps containing 108 loci on 11 linkage groups (LGs) were constructed for 227 families derived from this cross. Traits were measured in three replicated field trials conducted in New Zealand during the summers of 19971998, 19981999, and 20022003. The trials were managed to ensure maximum expression of yield potential. The QTL affecting yield-related traits were associated with 19 genomic regions on LGs I, II, III, IV, VI, and VII. The QTL for different yield-related traits were colocalized, suggesting some basis for understanding the reproductive plasticity that is observed in pea at the genetic level.
Abbreviations: AFLP, amplified fragment length polymorphism agpL2, ADP glucose pyrophosphorylase large subunit L2 CIM, composite interval mapping HI, harvest index LG, linkage group MAS, marker-assisted selection NFF, node of first flower NFN, number of flowering nodes NUM, seed number per plot or per square meter Px4, Primo x OSU442-15 QTL, quantitative trait loci RAPD, random amplified polymorphic DNA RFLP, restriction fragment length polymorphism sAFP, allele-specific polymerase chain reaction marker derived from an amplified fragment length polymorphism SPS, sucrose phosphate synthase STS, sequence tagged site SUS, sucrose synthase TNN, total node number TSW, 1000-seed weight
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