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首页> 外文期刊>Breeding science >Development of genome-wide PCR-based markers from insertion, deletion and single nucleotide polymorphisms for closely related Japanese rice cultivars and identification of QTLs for the appearance of cooked rice and polished rice
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Development of genome-wide PCR-based markers from insertion, deletion and single nucleotide polymorphisms for closely related Japanese rice cultivars and identification of QTLs for the appearance of cooked rice and polished rice

机译:从紧密相关的日本水稻品种的插入,缺失和单核苷酸多态性开发全基因组基于PCR的标记,并鉴定出米饭和精米的QTL

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摘要

Appearance of rice grain is an important property, affecting its acceptance by consumers. Moreover, appearance is a complex characteristic involving many components, including glossiness and whiteness. The genetic bases for the glossiness of cooked rice and the whiteness of polished rice (WPR) were determined using 133 recombinant inbred lines (RILs) derived from a cross between two closely related cultivars from Hokkaido, Joiku462, with high glossiness and whiteness, and Yukihikari, an ancestor of Joiku462 with low glossiness and whiteness. Analyses identified 167 genome-wide InDel markers, five cleaved amplified polymorphic sequences (CAPS) and eight derived CAPS markers differentiating the parental lines. The glossiness area (GLA) and glossiness strength (GLS) of cooked rice and WPR were determined for RILs in two locations, Pippu and Sapporo, Hokkaido. Four QTLs were detected. qGLA10 and qGLS9 were detected on chromosomes 10 and 9, respectively, with both being significant at both geographic locations. qWPR1 on chromosome 1 was significant at Pippu, and qWPR4 on chromosome 4 was significant at Sapporo. The Joiku462 alleles at all QTLs increased each trait. The PCR-based markers flanking these four QTLs may be useful for improvement of GLA, GLS and WPR.
机译:米粒的外观是重要的特性,影响其被消费者接受。而且,外观是涉及许多成分的复杂特征,包括光泽度和白度。使用133个重组自交系(RIL)来确定米饭的光泽度和精米的白度(WPR)的遗传基础,这些自交系来自北海道两个亲缘关系密切的品种Joiku462,具有较高的光泽度和白度,以及Yukihikari是Joiku462的祖先,其光泽度和白度低。分析确定了167个全基因组InDel标记,五个裂解的扩增多态性序列(CAPS)和八个衍生的区分亲本系的CAPS标记。在北海道皮普普和札幌两个地区的RIL中确定了米饭和WPR的米饭光泽度区域(GLA)和光泽度强度(GLS)。检测到四个QTL。 qGLA10和qGLS9分别在10号和9号染色体上检测到,在两个地理位置上均很重要。染色体1上的qWPR1在Pippu处显着,而染色体4上的qWPR4在札幌处显着。所有QTL的Joiku462等位基因均增加了每个性状。这四个QTL两侧的基于PCR的标记可能有助于改善GLA,GLS和WPR。

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