Wang Shukai, Wang Yancui, Xu Xitong, Lu Dusheng, Li Baokun, Zhao Yuxin, Cheng Senan, Li Zhenhong, Chen Cuixia
College of Agronomy, Shandong Agricultural University, Taian, Shandong, China.
PeerJ. 2025 Mar 31;13:e19143. doi: 10.7717/peerj.19143. eCollection 2025.
Kernel row number (KRN) is a crucial trait in maize that has a high impact on yield. However, KRN is a typical quantitative trait with only a few genes being verified so far. Here, two maize inbred lines with contrasting KRN were used to perform transcriptome analysis at five early ear developmental stages. Pairwise differential gene expression analyses were performed, and a total of 11,897 line-specific differentially expressed genes (DEGs) were detected between the two lines across the five development stages. Clustering analysis of line-specific DEGs revealed that the trends of gene expression changed significantly in the five stages, thus the five stages were further divided into two development phases: Phase I (V6-V8) and Phase II (V9-V10). Gene ontology enrichment analysis revealed that different transcriptional pathways were activated in the two phases. DEGs in Phase I were significantly enriched in morphogenesis and differentiation processes and hormone regulation. Of the 5,850 line-specific DEGs in Phase I, 2,132 genes were in known quantitative trait loci (QTLs) or flanking regions of quantitative trait nucleotides (QTNs), of which 92 were repeatedly detected in QTLs where QTNs also exist. The 92 high-probability candidate genes included development-related transcription factors (SBP-box and AP2/EREBP TFs) as well as genes involved in hormone homeostasis and signaling. Our study provides genetic resources for the elucidation of the molecular mechanisms of KRN development and reference for the cloning of candidate genes.
穗行数(KRN)是玉米中的一个关键性状,对产量有很大影响。然而,KRN是一个典型的数量性状,到目前为止只有少数基因得到验证。在这里,使用两个穗行数差异较大的玉米自交系在五个早期穗发育阶段进行转录组分析。进行了成对差异基因表达分析,在五个发育阶段共检测到11897个品系特异性差异表达基因(DEG)。对品系特异性DEG进行聚类分析,发现基因表达趋势在五个阶段有显著变化,因此将这五个阶段进一步分为两个发育阶段:第一阶段(V6-V8)和第二阶段(V9-V10)。基因本体富集分析表明,两个阶段激活了不同的转录途径。第一阶段的DEG在形态发生和分化过程以及激素调节方面显著富集。在第一阶段的5850个品系特异性DEG中,有2132个基因位于已知的数量性状位点(QTL)或数量性状核苷酸(QTN)的侧翼区域,其中92个在同时存在QTN的QTL中被重复检测到。这92个高概率候选基因包括与发育相关的转录因子(SBP-box和AP2/EREBP TFs)以及参与激素稳态和信号传导的基因。我们的研究为阐明KRN发育的分子机制提供了遗传资源,并为候选基因的克隆提供了参考。