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Mapping and validation of a major QTL for primary root length of soybean seedlings grown in hydroponic conditions

机译:水培条件生长的大豆幼苗初级根长的主要QTL的映射和验证

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Abstract Background The root system provides nutrient absorption and is closely related to abiotic stress tolerance, but it is difficult to study the roots under field conditions. This study was conducted to identify quantitative trait loci (QTL) associated with primary root length (PRL) during soybean seedling growth in hydroponic conditions. A total of 103 F 7 recombinant inbred lines (RILs) derived from a cross between K099 (short primary root) and Fendou 16 (long primary root) were used to identify QTL for PRL in soybean. The RIL population was genotyped with 223 simple sequence repeats markers covering 20 chromosomes. Phenotyping for primary root length was performed for 3-weeks plants grown in hydoponic conditions. The identified QTL was validated in near isogenic lines and in a separate RIL population. Results QTL analysis using inclusive composite interval mapping method identified a major QTL on Gm16 between SSR markers Sat_165 and Satt621, explaining 30.25?% of the total phenotypic variation. The identified QTL, qRL16.1 , was further confirmed in a segregating population derived from a residual heterozygous line (RHLs-98). To validate qRL16.1 ?in a different genetic background, QTL analysis was performed in another F 6 RIL population derived from a cross between Union (medium primary root) and Fendou 16, in which a major QTL was detected again in the same genomic region as qRL16.1 , explaining 14?% of the total phenotypic variation for PRL. In addition, the effect of qRL16.1 was confirmed using two pair of near-isogenic lines (NILs). PRL was significantly higher in NILs possessing the qRL16.1 allele from Fendou 16 compared to allele from K099. Conclusions The qRL16.1 ?is a novel QTL for primary root length in soybean which provides important information on the genetic control of root development. Identification of this major QTL will facilitate positional cloning and DNA marker-assisted selection for root traits in soybean.
机译:摘要背景根系提供营养吸收性,与非生物胁迫耐受性密切相关,但难以在现场条件下研究根源。进行该研究以鉴定水培条件下大豆幼苗生长期间与原母根长(PRL)相关的定量性状点(QTL)。总共103°F 7重组近交系(RILS)衍生自K099(短发根)和Fendou16(长主要根部)之间的横截面衍生的横截面,用于在大豆中鉴定PRL的QTL。 RIL群体是基因分型,223个简单序列重复标记覆盖20染色体。在卫渗条件生长的3周龄植物中进行初级根长度的表型。所识别的QTL在近同学线和单独的群体中验证。结果QTL分析采用包含复合间隔映射方法识别在SSR标记SAT_165和SATT621之间的GM16上的主要QTL,解释总表型变异的30.25倍。鉴定的QT1,QR116.1进一步在衍生自残留杂合线(RHLS-98)的分离群体中。为了验证QRL16.1?在不同的遗传背景下,QTL分析在来自联合(中等原色根)和Fendou 16之间的交叉之间的另一F 6 Ril群体中进行,其中在同一基因组区域中再次检测到主要QT1作为QR116.1,解释PRL总表型变异的14%。此外,使用两对近代碱基(NIL)确认QRL16.1的效果。与来自K099的等位基因相比,PRL在Fendou 16的QR116.1等位基因中显着高。结论QRL16.1?是大豆中原代根长的新型QTL,提供了关于根系发展的遗传控制的重要信息。该主要QTL的鉴定将促进大豆中的根部性状的位置克隆和DNA标记辅助选择。

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