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Identification of QTLs controlling grain protein concentration using a high-density SNP and SSR linkage map in barley (Hordeum vulgare L.)

机译:在大麦(Hordeum Vulgare L.)中使用高密度SNP和SSR联系地图控制谷物蛋白质浓度的QTLS

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摘要

Abstract Background Grain protein concentration (GPC) is a major determinant of quality in barley (Hordeum vulgare L.). Breeding barley cultivars with high GPC has practical value for feed and food properties. The aim of the present study was to identify quantitative trait loci (QTLs) for GPC that could be detected under multiple environments. Results A population of 190 recombinant inbred lines (RILs) deriving from a cross between Chinese landrace ZGMLEL with high GPC (> 20%) and Australian cultivar Schooner was used for linkage and QTL analyses. The genetic linkage map spanned 2353.48 cM in length with an average locus interval of 2.33 cM. GPC was evaluated under six environments for the RIL population and the two parental lines. In total, six environmentally stable QTLs for GPC were detected on chromosomes 2H (1), 4H (1), 6H (1), and 7H (3) and the increasing alleles were derived from ZGMLEL. Notably, the three QTLs on chromosome 7H (QGpc.ZiSc-7H.1, QGpc.ZiSc-7H.2, and QGpc.ZiSc-7H.3) that linked in coupling phase were firstly identified. Moreover, the genetic effects of stable QTLs on chromosomes 2H, 6H and 7H were validated using near isogenic lines (NILs). Conclusions Collectively, the identified QTLs expanded our knowledge about the genetic basis of GPC in barley and could be selected to develop cultivars with high grain protein concentration.
机译:摘要背景谷物蛋白质浓度(GPC)是大麦(Hordeum Vulgare L)质量的主要决定因素。具有高GPC的繁殖大麦品种具有饲料和食品特性的实用价值。本研究的目的是鉴定可以在多种环境下检测到的GPC的定量性状基因座(QTLS)。结果衍生自中国地拉尔Zgmle之间的十字串(> 20%)和澳大利亚品种Schooner之间的190种重组自交系(RILS)的群体,用于联系和QTL分析。遗传键映射的长度截止了2353.48cm,平均轨迹间隔为2.33厘米。 GPC在六个环境下评估RIL人口和两个父母。在染色体2H(1),4H(1),6H(1)和7H(3)上检测六种环境稳定的GPC QTLS,并且衍生自Zgmlel的增加的等位基因。值得注意的是,首先鉴定了在偶联阶段连接的染色体7h(QGPC.ZISC-7H.1,QGPC.ZISC-7H.1,QGPC.ZISC-7H.3)上的三个QTL。此外,使用近代型线(NIL)验证了稳定QTL对染色体2H,6H和7H的遗传效应。结论集体,所确定的QTLS扩大了我们对大麦GPC遗传基础的了解,并且可以选择开发具有高晶粒蛋白质浓度的品种。

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