College of Agronomy, Anhui Agricultural University, Key Laboratory of Wheat Biology and Genetic Improvement on Southern Yellow & Huai River Valley, Ministry of Agriculture, Hefei, 230036, Anhui, China.
Theor Appl Genet. 2024 Feb 24;137(3):57. doi: 10.1007/s00122-024-04564-6.
Ten stable loci for freezing tolerance (FT) in wheat were detected by genome-wide association analysis. The putative candidate gene TaRPM1-7BL underlying the major locus QFT.ahau-7B.2 was identified and validated. Frost damage restricts wheat growth, development, and geographical distribution. However, the genetic mechanism of freezing tolerance (FT) remains unclear. Here, we evaluated FT phenotypes of 245 wheat varieties and lines, and genotyped them using a Wheat 90 K array. The association analysis showed that ten stable loci were significantly associated with FT (P < 1 × 10), and explained 6.45-26.33% of the phenotypic variation. In particular, the major locus QFT.ahau-7B.2 was consistently related to all nine sets of FT phenotypic data. Based on five cleaved amplified polymorphic sequence (CAPS) markers closely linked to QFT.ahau-7B.2, we narrowed down the target region to the 570.67-571.16 Mb interval (0.49 Mb) on chromosome 7B, in which four candidate genes were annotated. Of these, only TaRPM1-7BL exhibited consistent differential expression after low temperature treatment between freezing-tolerant and freezing-sensitive varieties. The results of cloning and whole-exome capture sequencing indicated that there were two main haplotypes for TaRPM1-7BL, including freezing-tolerant Hap1 and freezing-sensitive Hap2. Based on the representative SNP (+1956, A/G), leading to an amino acid change in the NBS domain, a CAPS marker (CAPS-TaRPM1-7BL) was developed and validated in 431 wheat varieties (including the above 245 materials) and 318 F lines derived from the cross of 'Annong 9267' (freezing-tolerant) × 'Yumai 9' (freezing-sensitive). Subsequently, the TaRPM1-7BL gene was silenced in 'Yumai 9' by virus-induced gene silencing (VIGS), and these silenced wheat seedlings exhibited enhanced FT phenotypes, suggesting that TaRPM1-7BL negatively regulates FT. These findings are valuable for understanding the complex genetic basis of FT in wheat.
通过全基因组关联分析,在小麦中检测到了 10 个耐冻结性(FT)的稳定基因座。在主要基因座 QFT.ahau-7B.2 下鉴定并验证了候选基因 TaRPM1-7BL。霜害限制了小麦的生长、发育和地理分布。然而,耐冻结性(FT)的遗传机制仍不清楚。在这里,我们评估了 245 个小麦品种和系的 FT 表型,并使用小麦 90K 芯片对它们进行了基因型分析。关联分析表明,十个稳定的基因座与 FT 显著相关(P < 1 × 10),解释了 6.45-26.33%的表型变异。特别是,主要基因座 QFT.ahau-7B.2 与所有九组 FT 表型数据均相关。基于与 QFT.ahau-7B.2 紧密连锁的五个切割扩增多态性序列(CAPS)标记,我们将目标区域缩小到 7B 染色体上的 570.67-571.16 Mb 区间(0.49 Mb),其中注释了四个候选基因。其中,只有 TaRPM1-7BL 在耐冻和敏感品种之间的低温处理后表现出一致的差异表达。克隆和外显子捕获测序的结果表明,TaRPM1-7BL 有两个主要的单倍型,包括耐冻 Hap1 和敏感 Hap2。基于代表性 SNP(+1956,A/G),导致 NBS 结构域的氨基酸改变,开发并验证了 CAPS 标记(CAPS-TaRPM1-7BL),该标记在 431 个小麦品种(包括上述 245 个材料)和 318 个“安农 9267”(耐冻)ד豫麦 9”(敏感)杂交后代的 F 代中进行了验证。随后,通过病毒诱导基因沉默(VIGS)使“豫麦 9”中的 TaRPM1-7BL 基因沉默,这些沉默的小麦幼苗表现出增强的 FT 表型,表明 TaRPM1-7BL 负调控 FT。这些发现有助于理解小麦中 FT 的复杂遗传基础。