INRA, Station d'Amélioration des Plantes Maraîchères, BP 94, 84143, Montfavet Cedex, France.
Theor Appl Genet. 1996 Jul;93(1-2):57-64. doi: 10.1007/BF00225727.
One hundred and ten markers were analysed for linkage in 218 F2 plants derived from two divergent cultivars ('Védrantais' and 'Songwhan Charmi') of Cucumis melo (L.). Thirty-four RFLPs, 64 RAPDs, one isozyme, four disease resistance markers and one morphological marker were used to construct a genetic map spanning 14 linkage groups covering 1390 cM of the melon genome. RAPD and RFLP markers detected similar polymorphism levels. RFLPs were largely due to base substitutions rather than insertion/deletions. Twelve percent of markers showed distorted segregation. Phenotypic markers consisted of two resistance genes against Fusarium wilt (Fom-1 and Fom-2), one gene (nsv) controlling the resistance to melon necrotic spot virus, one gene (Vat) conferring resistance to Aphis gossypii, and a recessive gene for carpel numbers (3 vs 5 carpels: p).
110 个标记被分析连锁在 218 株 F2 植株中,这些植株来自于两个不同的甜瓜品种(‘Védrantais’和‘Songwhan Charmi’)。34 个 RFLP、64 个 RAPD、一个同工酶、4 个抗病标记和 1 个形态标记被用于构建一张遗传图谱,图谱覆盖了甜瓜基因组的 1390cM,包含 14 个连锁群。RAPD 和 RFLP 标记检测到相似的多态性水平。RFLP 主要是由于碱基替换而不是插入/缺失。12%的标记显示偏分离。表型标记包括两个抗镰刀菌枯萎病的基因(Fom-1 和 Fom-2)、一个控制对甜瓜坏死斑点病毒抗性的基因(nsv)、一个抗棉蚜的基因(Vat),以及一个隐性基因控制心皮数量(3 个 vs 5 个心皮:p)。