Key Laboratory of Grain Crop Genetic Resources Evaluation and Utilization (MARA), The National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences (ICS-CAAS), Beijing 100081, China; Hainan Yazhou Bay Seed Laboratory, Sanya 572025, China.
Key Laboratory of Grain Crop Genetic Resources Evaluation and Utilization (MARA), The National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences (ICS-CAAS), Beijing 100081, China; Institute of Industrial Crops, Shandong Academy of Agricultural Sciences, Jinan 250100, China.
Plant Commun. 2024 Jan 8;5(1):100670. doi: 10.1016/j.xplc.2023.100670. Epub 2023 Aug 9.
Grain number, one of the major determinants of yield in Triticeae crops, is largely determined by spikelet number and spike rachis node number (SRN). Here, we identified three quantitative trait loci (QTLs) for SRN using 145 recombinant inbred lines derived from a barley R90/1815D cross. qSRN1, the major-effect QTL, was mapped to chromosome 2H and explained up to 38.77% of SRN variation. Map-based cloning revealed that qSRN1 encodes the RAWUL domain-containing protein HvSRN1. Further analysis revealed that two key SNPs in the HvSRN1 promoter region (∼2 kb upstream of the transcription start site) affect the transcript level of HvSRN1 and contribute to variation in SRN. Similar to its orthologous proteins OsLAX2 and ZmBA2, HvSRN1 showed protein-protein interactions with HvLAX1, suggesting that the LAX2-LAX1 model for spike morphology regulation may be conserved in Poaceae crops. CRISPR-Cas9-induced HvSRN1 mutants showed reduced SRN but increased grain size and weight, demonstrating a trade-off effect. Our results shed light on the role of HvSRN1 variation in regulating the balance between grain number and weight in barley.
粒数是禾本科作物产量的主要决定因素之一,主要由小穗数和穗轴节数(SRN)决定。在这里,我们利用来源于大麦 R90/1815D 杂交的 145 个重组自交系鉴定了三个与 SRN 相关的数量性状位点(QTL)。qSRN1 是一个主效 QTL,被定位在 2H 染色体上,解释了高达 38.77%的 SRN 变异。基于图谱的克隆表明 qSRN1 编码 RAWUL 结构域蛋白 HvSRN1。进一步分析表明,HvSRN1 启动子区域(转录起始位点上游约 2kb)的两个关键 SNP 影响 HvSRN1 的转录水平,导致 SRN 变异。与它的同源蛋白 OsLAX2 和 ZmBA2 相似,HvSRN1 与 HvLAX1 表现出蛋白-蛋白相互作用,表明 LAX2-LAX1 模型在禾本科作物的穗形态调控中可能是保守的。CRISPR-Cas9 诱导的 HvSRN1 突变体显示出 SRN 减少,但粒重和粒重增加,表现出权衡效应。我们的研究结果揭示了 HvSRN1 变异在调节大麦中粒数和粒重平衡中的作用。