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Fruit weight is controlled by Cell Size Regulator encoding a novel protein that is expressed in maturing tomato fruits

机译:果实的重量由细胞大小调节剂控制,该大小编码器编码一种在成熟番茄果实中表达的新型蛋白质

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Increases in fruit weight of cultivated vegetables and fruits accompanied the domestication of these crops. Here we report on the positional cloning of a quantitative trait locus (QTL) controlling fruit weight in tomato. The derived allele of Cell Size Regulator (CSR-D) increases fruit weight predominantly through enlargement of the pericarp areas. The expanded pericarp tissues result from increased mesocarp cell size and not from increased number of cell layers. The effect of CSR on fruit weight and cell size is found across different genetic backgrounds implying a consistent impact of the locus on the trait. In fruits, CSR expression is undetectable early in development from floral meristems to the rapid cell proliferation stage after anthesis. Expression is low but detectable in growing fruit tissues and in or around vascular bundles coinciding with the cell enlargement stage of the fruit maturation process. CSR encodes an uncharacterized protein whose clade has expanded in the Solanaceae family. The mutant allele is predicted to encode a shorter protein due to a 1.4 kb deletion resulting in a 194 amino-acid truncation. Co-expression analyses and GO term enrichment analyses suggest association of CSR with cell differentiation in fruit tissues and vascular bundles. The derived allele arose in Solanum lycopersicum var cerasiforme and appears completely fixed in many cultivated tomato’s market classes. This finding suggests that the selection of this allele was critical to the full domestication of tomato from its intermediate ancestors.
机译:随着这些农作物的驯化,栽培蔬菜和水果的果实重量增加。在这里,我们报告了控制番茄果实重量的数量性状基因座(QTL)的位置克隆。细胞大小调节剂(CSR-D)的衍生等位基因主要通过扩大果皮面积来增加果实重量。果皮组织的扩张是由于中果皮细胞大小增加而引起的,而不是由于细胞层数增加而引起的。在不同的遗传背景下发现了CSR对果实重量和细胞大小的影响,这暗示了基因座对性状的一致影响。在水果中,从花分生组织到开花后的快速细胞增殖阶段的早期,无法检测到CSR表达。表达较低,但在生长的果实组织中以及在血管束中或周围的血管束中可检测到,这与果实成熟过程的细胞扩大阶段相吻合。 CSR编码一个未鉴定的蛋白质,其进化枝已在茄科中扩展。由于1.4 kb的缺失导致194个氨基酸的截短,因此突变等位基因预计编码较短的蛋白质。共表达分析和GO术语富集分析表明,CSR与水果组织和维管束中的细胞分化有关。衍生的等位基因出现在番茄茄中,并在许多栽培番茄的市场类别中完全固定。这一发现表明,该等位基因的选择对于从其中间祖先完全驯化番茄至关重要。

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