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A Putative Gene sbe3-rs for Resistant Starch Mutated from SBE3 for Starch Branching Enzyme in Rice (Oryza sativa L.)

机译:推定的基因sbe3-Rs为抗性淀粉突变从sBE3用于淀粉分支酶在水稻(Oryza sativa L.)

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摘要

Foods high in resistant starch (RS) are beneficial to prevent various diseases including diabetes, colon cancers, diarrhea and chronic renal or hepatic diseases. Elevated RS in rice is important for public health since rice is a staple food for half of the world population. A japonica mutant ‘Jiangtangdao 1’ (RS = 11.67%) was crossed with an indica cultivar ‘Miyang 23’ (RS = 0.41%). The mutant sbe3-rs that explained 60.4% of RS variation was mapped between RM6611 and RM13366 on chromosome 2 (LOD = 36) using 178 F2 plants genotyped with 106 genome-wide polymorphic SSR markers. Using 656 plants from four F3∶4 families, sbe3-rs was fine mapped to a 573.3 Kb region between InDel 2 and InDel 6 using one STS, five SSRs and seven InDel markers. SBE3 which codes for starch branching enzyme was identified as a candidate gene within the putative region. Nine pairs of primers covering 22 exons were designed to sequence genomic DNA of the wild type for SBE3 and the mutant for sbe3-rs comparatively. Sequence analysis identified a missense mutation site where Leu-599 of the wild was changed to Pro-599 of the mutant in the SBE3 coding region. Because the point mutation resulted in the loss of a restriction enzyme site, sbe3-rs was not digested by a CAPS marker for SpeI site while SBE3 was. Co-segregation of the digestion pattern with RS content among 178 F2 plants further supported sbe3-rs responsible for RS in rice. As a result, the CAPS marker could be used in marker-assisted breeding to develop rice cultivars with elevated RS which is otherwise difficult to accurately assess in crops. Transgenic technology should be employed for a definitive conclusion of the sbe3-rs.
机译:高抗性淀粉(RS)的食物有助于预防各种疾病,包括糖尿病,结肠癌,腹泻和慢性肾脏或肝病。稻米中的RS升高对于公共卫生非常重要,因为稻米是世界一半人口的主食。将粳稻突变体“江塘刀1”(RS = 11.67%)与in稻品种“ Miyang 23”(RS = 0.41%)杂交。使用178种F106植物进行了106个基因组范围的多态性SSR标记基因型分析,解释了60.4%RS变异的突变体sbe3-rs位于2号染色体上的RM6611和RM13366之间(LOD = 36)。使用来自四个F3∶4家族的656株植物,使用一个STS,五个SSR和七个InDel标记将sbe3-rs精细定位到InDel 2和InDel 6之间的573.3 Kb区域。编码淀粉分支酶的SBE3被鉴定为推定区域内的候选基因。设计九对覆盖22个外显子的引物,以对SBE3的野生型基因组DNA和sbe3-rs的突变体进行相对测序。序列分析鉴定了一个错义突变位点,其中在SBE3编码区中,野生的Leu-599变成了突变的Pro-599。因为点突变导致限制性内切酶位点的丢失,所以sbe3-rs不会被SpeI位点的CAPS标记消化,而SBE3则不会。 178种F2植物中消化模式与RS含量的共分离进一步支持了负责水稻中RS的sbe3-rs。因此,CAPS标记可用于标记辅助育种,以开发RS升高的水稻品种,否则很难在作物中准确评估。应该使用转基因技术来确定sbe3-rs。

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