Comparative transcriptome analysis identified candidate genes associated with kernel row number in maize

被引:0
作者
Wang, Shukai [1 ]
Wang, Yancui [1 ]
Xu, Xitong [1 ]
Lu, Dusheng [1 ]
Li, Baokun [1 ]
Zhao, Yuxin [1 ]
Cheng, Senan [1 ]
Li, Zhenhong [1 ]
Chen, Cuixia [1 ]
机构
[1] Shandong Agr Univ, Coll Agron, Tai An, Shandong, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Kernel row number; Quantitative trait locus; Comparative transcriptome; Maize; INFLORESCENCE ARCHITECTURE; MERISTEM DEVELOPMENT; GRAIN-YIELD; TRAITS; EAR; COMPONENTS; PRIMORDIA; LINKAGE; HISAT; QTL;
D O I
10.7717/peerj.19143
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:22
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