HIGH-RESOLUTION MAPPING AND ISOLATION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG CONTAINING FW2.2 - A MAJOR FRUIT WEIGHT QUANTITATIVE TRAIT LOCUS IN TOMATO
Kb. Alpert et Sd. Tanksley, HIGH-RESOLUTION MAPPING AND ISOLATION OF A YEAST ARTIFICIAL CHROMOSOME CONTIG CONTAINING FW2.2 - A MAJOR FRUIT WEIGHT QUANTITATIVE TRAIT LOCUS IN TOMATO, Proceedings of the National Academy of Sciences of the United Statesof America, 93(26), 1996, pp. 15503-15507
A high-resolution physical and genetic map of a major fruit weight qua
ntitative trait locus (QTL), fw2.2, has been constructed for a region
of tomato chromosome 2. Using an F-2 nearly isogenic line mapping popu
lation (3472 individuals) derived from Lycopersicon esculentum (domest
icated tomato) x Lycopersicon pennellii (wild tomato), fw2.2 has been
placed near TG91 and TG167, which have an interval distance of 0.13 +/
- 0.03 centimorgan. The physical distance between TG91 and TG167 was e
stimated to be less than or equal to 150 kb by pulsed-field gel electr
ophoresis of tomato DNA. A physical contig composed of six yeast artif
icial chromosomes (YACs) and encompassing fw2.2 was isolated. No rearr
angements or chimerisms were detected within the YAC contig based on r
estriction fragment length polymorphism analysis using YAC-end sequenc
es and anchored molecular markers from the high-resolution map. Based
on genetic recombination events, fw2.2 could be narrowed down to a reg
ion less than 150 kb between molecular markers TG91 and HSF24 and incl
uded within two YACs: YAC264 (210 kb) and YAC355 (300 kb). This marks
the first time, to our knowledge, that a QTL has been mapped with such
precision and delimited to a segment of cloned DNA. The fact that the
phenotypic effect of the fw2.2 QTL can be mapped to a small interval
suggests that the action of this QTL is likely due to a single gene. T
he development of the high-resolution genetic map, in combination with
the physical YAC contig, suggests that the gene responsible for this
QTL and other QTLs in plants can be isolated using a positional clonin
g strategy. The cloning of fw2.2 will likely lead to a better understa
nding of the molecular biology of fruit development and to the genetic
engineering of fruit size characteristics.