Maize Research Institute, Sichuan Agricultural University, No.211 Huiming Road, Wenjiang District, Chengdu, 611130, Sichuan, China.
School of Life Science and Engineering, Southwest University of Science and Technology, Mianyang, China.
Theor Appl Genet. 2024 Nov 18;137(12):271. doi: 10.1007/s00122-024-04780-0.
Two closely linked novel loci, qKRN2-1 and qKRN2-2, associated with kernel row number were fine-mapped on chromosome 2, and a key candidate gene for qKRN2-1 was identified through expression analysis. Kernel row number (KRN) is a crucial factor influencing maize yield and serves as a significant target for maize breeding. The use of wild progenitor species can aid in identifying the essential traits for domestication and breeding. In this study, teosinte (MT1) served as the donor parent, the inbred maize line of Mo17 was used as the recurrent parent, we identified a major quantitative trait locus (QTL) for KRN, designated qKRN2, into two closely linked loci, qKRN2-1 and qKRN2-2. Here, fine mapping was performed to investigate two QTLs, qKRN2-1 and qKRN2-2, within a genomic range of 272 kb and 775 kb, respectively. This was achieved using a progeny test strategy in an advanced backcross population, with the two QTLs explaining 33.49% and 35.30% of the phenotypic variance. Molecular marker-assisted selection resulted in the development of two nearly isogenic lines (NILs), qKRN2-1 and qKRN2-2, which differed only in the segment containing the QTL. Notably, the maize (Mo17) alleles increased the KRN relative to teosinte by approximately 1.4 and 1.2 rows for qKRN2-1 and qKRN2-2, respectively. Zm00001d002989 encodes a cytokinin oxidase/dehydrogenase and its expression in the immature ears exhibited significant differences among the qKRN2-1 NILs. In situ hybridization localized Zm00001d002989 to the primordia of the inflorescence meristem and spikelet pair meristems, is predicted to be the causal gene of qKRN2-1. The findings of this study deepen our understanding of the genetic basis of KRN and hold significant potential for improving maize grain yields.
两个紧密连锁的新基因座 qKRN2-1 和 qKRN2-2 与穗行数相关,被精细定位在 2 号染色体上,并通过表达分析鉴定到 qKRN2-1 的一个关键候选基因。穗行数(KRN)是影响玉米产量的关键因素,也是玉米育种的重要目标。利用野生祖本可以帮助鉴定驯化和育种的关键性状。在这项研究中,以墨西哥玉米为供体亲本,以自交系 Mo17 为轮回亲本,我们鉴定到一个控制穗行数的主效数量性状位点(QTL),命名为 qKRN2,该 QTL 被精细定位到两个紧密连锁的基因座 qKRN2-1 和 qKRN2-2。在这里,我们使用一个衍生测验群体对这两个 QTL 进行了精细定位,分别在 272kb 和 775kb 的基因组范围内进行了定位。两个 QTL 解释了表型方差的 33.49%和 35.30%。利用分子标记辅助选择开发了两个近等基因系(NIL),qKRN2-1 和 qKRN2-2,它们在包含 QTL 的片段上存在差异。值得注意的是,相对于墨西哥玉米,qKRN2-1 和 qKRN2-2 的玉米(Mo17)等位基因分别使穗行数增加了大约 1.4 和 1.2 行。Zm00001d002989 编码细胞分裂素氧化酶/脱氢酶,其在未成熟穗中的表达在 qKRN2-1 NIL 之间存在显著差异。原位杂交将 Zm00001d002989 定位到花序分生组织和小穗对分生组织的原基上,预计是 qKRN2-1 的候选基因。本研究加深了我们对 KRN 遗传基础的理解,对提高玉米籽粒产量具有重要意义。