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Accelerating public sector rice breeding with high-density KASP markers derived from whole genome sequencing of indica rice

机译:用籼稻全基因组测序的高密度kasp标记加速公共部门水稻育种

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Few public sector rice breeders have the capacity to use NGS-derived markers in their breeding programmes despite rapidly expanding repositories of rice genome sequence data. They rely on & 18,000 mapped microsatellites (SSRs) for marker- assisted selection (MAS) using gel analysis. Lack of knowledge about target SNP and InDel variant loci has hampered the uptake by many breeders of Kompetitive allele-specific PCR (KASP), a proprietary technology of LGC genomics that can distinguish alleles at variant loci. KASP is a cost-effective single-step genotyping technology, cheaper than SSRs and more flexible than genotyping by sequencing (GBS) or array-based genotyping when used in selection programmes. Before this study, there were 2015 rice KASP marker loci in the public domain, mainly identified by array-based screening, leaving large proportions of the rice genome with no KASP coverage. Here we have addressed the urgent need for a wide choice of appropriate rice KASP assays and demonstrated that NGS can detect many more KASP to give full genome coverage. Through resequencing of nine indica rice breeding lines or released varieties, this study has identified 2.5 million variant sites. Stringent filtering of variants generated 1.3 million potential KASP assay designs, including 92,500 potential functional markers. This strategy delivers a 650-fold increase in potential selectable KASP markers at a density of 3.1 per 1 kb in the indica crosses analysed and 377,178 polymorphic KASP design sites on average per cross. This knowledge is available to breeders and has been utilised to improve the efficiency of public sector breeding in Nepal, enabling identification of polymorphic KASP at any region or quantitative trait loci in relevant crosses. Validation of 39 new KASP was carried out by genotyping progeny from a range of crosses to show that they detected segregating alleles. The new KASP have replaced SSRs to aid trait selection during marker-assisted backcrossing in these crosses, where target traits include rice blast and BLB resistance loci. Furthermore, we provide the software for plant breeders to generate KASP designs from their own datasets.
机译:尽管快速扩展了水稻基因组序列数据的储存库,但少数公共部门稻育植物在其繁殖计划中有能力在其繁殖计划中使用NGS衍生的标志。他们依靠& 用于使用凝胶分析的标记辅助选择(MAS)的18,000次映射微透露型(SSR)。缺乏关于目标SNP和Indel Variant Loci的知识阻碍了许多特异性异位等级PCR(KASP)的许多育种者的摄取,LGC基因组学的专有技术可以区分变体基因座的等位基因。 Kasp是一种经济有效的单步基因分型技术,比SSRS更便宜,而不是通过在选择程序中使用时通过测序(GBS)或基于阵列的基因分型更灵活。在这项研究之前,公共领域中有2015年的稻米kasp标记基因座,主要通过基于阵列的筛查确定,留下大量的水稻基因组,没有Kasp覆盖。在这里,我们解决了迫切需要各种各样的水稻kasp测定,并证明NGS可以检测到更多的kasp以提供全基因组覆盖。通过九种籼稻育种线或释放品种的重量,本研究确定了250万个变体部位。变形的严格滤波产生了130万潜在的凯拉斯测定设计,包括92,500个潜在的功能标记。该策略在籼稻交叉口中的3.1每1kb的密度和377,178多态性Kasp设计网站上的密度提供650倍的潜在可选凯拉斯标记。这种知识可用于育种者,并且已被利用,以提高尼泊尔公共部门繁殖的效率,使得能够在相关交叉口中的任何区域或定量性状基因座的鉴定。通过基因分型后代从一系列十字形进行基因分型后代进行39个新kasp的验证,以表明它们检测到分离等位基因。新的Kasp已经取代了SSRS在这些十字架中的标记辅助回复期间辅助特征选择,其中靶性特征包括稻瘟病和飞行抵抗基因座。此外,我们为植物育种者提供软件,从他们自己的数据集生成Kasp设计。

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