Citrullus lanatus (Thunb.) Matsum. & Nakai - Cucurbit Breeding ...
Citrullus lanatus (Thunb.) Matsum. & Nakai - Cucurbit Breeding ...
Citrullus lanatus (Thunb.) Matsum. & Nakai - Cucurbit Breeding ...
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convenient than progeny selection, which requires an additional self-pollination and testing of the next<br />
generation. We were interested to determine whether molecular markers could be found for resistance to<br />
gummy stem blight.<br />
Molecular markers linked with resistance to gummy stem blight are not currently available.<br />
Nevertheless, linkage maps of watermelon have been constructed and several molecular markers are available<br />
(Hashizume et al., 2003; Hawkins et al., 2001; Levi et al., 2002; Zhang et al., 2004). Hawkins et al. (2001)<br />
constructed two partial maps from an F 2 and F 3 population, respectively, of the cross 'NH Midget' × PI 294361-<br />
FR. The two short maps were 112.9 centimorgans (cM) and 139 cM long and included 26 and 13 RAPD<br />
(random amplified polymorphic DNA) markers, respectively. In 2002, Levi et al. published a linkage map<br />
where 171 RAPD markers, 27 ISSR (inter-simple sequence repeats) markers, and one SCAR (sequence-<br />
characterized amplified region) marker were assigned to 24 linkage groups, the haploid number for watermelon<br />
being 11. The linkage map by Hashizume et al. (2003) included RAPD, RFLP (restriction fragment length<br />
polymorphism), and ISSR markers that mapped 554 loci in 11 linkage groups, for a total length of 2,384 cM.<br />
Finally in 2004, Zhang et al. constructed a linkage map from a population of 117 recombinant inbred lines<br />
(RILs) using a total of 104 RAPD, SCAR, and ISSR markers. The map covered a total distance of 1,027 cM<br />
and included 15 linkage groups.<br />
Additional molecular markers have been made available, but not mapped, for use in watermelon<br />
(Guerra-Sanz, 2002; Jarret et al., 1997; Katzir et al., 1996; Poleg et al., 2001). Katzir et al. (1996) identified<br />
SSR (simple sequence repeat) markers from DNA sequences of melon (Cucumis melo L.), watermelon, and<br />
cucumber (Cucumis sativus L.) that amplified DNA fragments also in cucurbit species different from the one of<br />
origin. In 1997, Jarret et al. used seven SSR markers to measure diversity among 32 watermelon lines. Poleg et<br />
al. (2001) designed 24 SSR markers from a genomic library of melon DNA, four from a cucumber cDNA<br />
library, and six from database sequences of cucumber and melon. Guerra–Sanz (2002) designed 19 primer pairs<br />
from watermelon ESTs (expressed sequence tag) containing SSR markers.<br />
Currently, the database of the National Center for Biotechnology Information (NCBI) contains 722<br />
nucleotidic sequences (mostly ESTs) for watermelon (NCBI, 2004). These sequences can be also used to<br />
design additional primers for amplification and screening of candidate sequence-based markers. A similar<br />
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