Wang Xi, Zhang Qiongqiong, Luo Junfeng, Liu Xin, Jiang Jing
College of Horticulture, Shenyang Agricultural University, Shenyang, 110866, Liaoning, China.
Key Laboratory of Protected Horticulture of Education Ministry, Shenyang, 110866, Liaoning, China.
Theor Appl Genet. 2023 Mar 27;136(4):88. doi: 10.1007/s00122-023-04351-9.
qLKR4.1, controlling low K resistance in tomato, was fine-mapped to an interval of 67.5 kb on chromosome A04, and one gene encoding phospholipase Dδ was identified as a candidate gene. In plants, changes in root length are an important morphological response to low K (LK) stress; however, the underlying genetics in tomato remain unclear. Here, we combined bulked segregant analysis-based whole-genome sequencing, single-nucleotide polymorphism haplotyping, and fine genetic mapping to identify a candidate gene as a major-effect quantitative trait loci (QTL), i.e., qLKR4.1, which was associated with LK tolerance due to increased root elongation in the tomato line JZ34. Through multiple analyses, we found that Solyc04g082000 is the most likely candidate for qLKR4.1, which encodes phospholipase Dδ (PLDδ). Increased root elongation under LK in JZ34 may be attributed to a non-synonymous single-nucleotide polymorphism in the Ca-binding domain region of this gene. Solyc04g082000 increases root length through its PLDδ activity. Silencing of Solyc04g082000 in JZ34 led to a significant decrease in root length compared with silencing of Solyc04g082000 allele in JZ18 under LK conditions. Mutation of a Solyc04g082000 homologue in Arabidopsis, pldδ, resulted in decreased primary root lengths under LK conditions, compared to the wild type. Transgenic tomato expressing the qLKR4.1 allele from JZ34 exhibited a significant increase in root length compared with the wild type expressing the allele from JZ18 under LK conditions. Taken together, our results confirm that the PLDδ gene Solyc04g082000 exerts important functions in increasing tomato root length and LK tolerance.
控制番茄低钾抗性的qLKR4.1被精细定位到A04染色体上67.5 kb的区间,并且一个编码磷脂酶Dδ的基因被鉴定为候选基因。在植物中,根长的变化是对低钾(LK)胁迫的一种重要形态学响应;然而,番茄中潜在的遗传学机制仍不清楚。在此,我们结合基于混合分组分析法的全基因组测序、单核苷酸多态性单倍型分析以及精细遗传定位,来鉴定一个候选基因作为主效数量性状位点(QTL),即qLKR4.1,它与番茄品系JZ34中因根伸长增加而产生的LK耐受性相关。通过多项分析,我们发现Solyc04g082000是qLKR4.1最有可能的候选基因,它编码磷脂酶Dδ(PLDδ)。JZ34在LK条件下根伸长增加可能归因于该基因钙结合结构域区域的一个非同义单核苷酸多态性。Solyc04g082000通过其PLDδ活性增加根长。在LK条件下,JZ34中Solyc04g082000的沉默导致根长显著降低,相比之下,JZ18中Solyc04g082000等位基因的沉默则不然。拟南芥中Solyc04g082000的同源基因pldδ发生突变后,与野生型相比,在LK条件下主根长度缩短。在LK条件下,与表达JZ18等位基因的野生型番茄相比,表达JZ34的qLKR4.1等位基因的转基因番茄根长显著增加。综上所述,我们的结果证实PLDδ基因Solyc04g082000在增加番茄根长和LK耐受性方面发挥着重要作用。