Department of Vegetable Crops, University of California, Davis, 95616-8746, Davis, CA, USA.
Theor Appl Genet. 1993 Oct;87(1-2):184-92. doi: 10.1007/BF00223763.
The germination responsiveness of an F2 population derived from the cross Lycopersicon esculentum (UCT5) x L. pennellii (LA716) was evaluated for salt tolerance at two stress levels, 150 mM NaCl + 15 mM CaCl2 and 200 mM NaCl + 20 mM CaCl2. Individuals were selected at both tails of the response distribution. The salt-tolerant and salt-sensitive individuals were genotyped at 16 isozyme loci located on 9 of the 12 tomato chromosomes. In addition, an unselected (control) F2 population was genotyped at the same marker loci, and gene frequencies were estimated in both selected and unselected populations. Trait-based marker analysis was effective in identifying genomic locations (quantitative trait loci, QTLs) affecting salt tolerance in the tomato. Three genomic locations marked by Est-3 on chromosome 1, Prx-7 on chromosome 3, and 6Pgdh-2 and Pgi-1 on chromosome 12 showed significant positive effects, while 2 locations associated with Got-2 on chromosome 7 and Aps-2 on chromosome 8 showed significant negative effects. The identification of genomic locations with both positive and negative effects on this trait suggests the likelihood of recovering transgressive segregants in progeny derived from these parental lines. Similar genomic locations were identified when selection was made either for salt tolerance or salt sensitivity and at both salt-stress treatments. Comparable results were obtained in uni- and bidirectional selection experiments. However, when marker allele gene frequencies in a control population are unknown, bidirectional selection may be more efficient than unidirectional selection in identifying marker-QTL associations. Results from this study are discussed in relationship to the use of molecular markers in developing salt-tolerant tomatoes.
利用 150mMNaCl+15mM CaCl2 和 200mMNaCl+20mM CaCl2 两种胁迫水平,评价了来自 Lycopersicon esculentum (UCT5)×L. pennellii (LA716)杂交 F2 群体的发芽响应对盐胁迫的耐受性。在响应分布的两个尾部选择个体。在 12 条番茄染色体中的 9 条染色体上的 16 个同工酶基因座对耐盐和盐敏感个体进行了基因分型。此外,对未选择的(对照)F2 群体在相同的标记基因座进行了基因分型,并在选择和未选择的群体中估计了基因频率。基于性状的标记分析有效地确定了影响番茄耐盐性的基因组位置(数量性状基因座,QTL)。在第 1 条染色体上用 Est-3、第 3 条染色体上用 Prx-7 以及第 12 条染色体上的 6Pgdh-2 和 Pgi-1 标记的 3 个基因组位置表现出显著的正效应,而与第 7 条染色体上的 Got-2 和第 8 条染色体上的 Aps-2 相关的 2 个位置则表现出显著的负效应。在该性状上鉴定出对基因组位置有正向和负向影响的情况表明,在这些亲本系的后代中,可能会恢复到具有较大偏度的分离体。在耐盐性或盐敏感性的选择中,以及在两种盐胁迫处理下,都鉴定出了类似的基因组位置。单向和双向选择实验均获得了类似的结果。然而,当控制群体中标记等位基因的基因频率未知时,与单向选择相比,双向选择在鉴定标记-QTL 关联时可能更有效。本研究的结果与利用分子标记开发耐盐番茄的问题有关。