QTL-seq and transcriptomic integrative analyses reveal two positively regulated genes that control the low-temperature germination ability of MTP-maize introgression lines
文献类型: 外文期刊
第一作者: He, Ru-Yu
作者: He, Ru-Yu;Zheng, Jun-Jun;Chen, Yu;Pan, Ze-Yang;Yang, Tao;Zhou, Yang;Li, Xiao-Feng;Nan, Xinyi;Li, Ying-Zheng;Iqbal, Muhammad-Zafar;He, Jian-Mei;Rong, Ting-Zhao;Tang, Qi-Lin;Cheng, Ming-Jun;Li, Yan;Li, Yang;Yan, Xu
作者机构:
期刊名称:THEORETICAL AND APPLIED GENETICS ( 影响因子:5.4; 五年影响因子:5.7 )
ISSN: 0040-5752
年卷期: 2023 年 136 卷 5 期
页码:
收录情况: SCI
摘要: Key messageTwo candidate genes (ZmbZIP113 and ZmTSAH1) controlling low-temperature germination ability were identified by QTL-seq and integrative transcriptomic analyses. The functional verification results showed that two candidate genes positively regulated the low-temperature germination ability of IB030.Low-temperature conditions cause slow maize (Zea mays L.) seed metabolism, resulting in slow seedling emergence and irregular seedling emergence, which can cause serious yield loss. Thus, improving a maize cultivar's low-temperature germination ability (LTGA) is vital for increasing yield production. Wild relatives of maize, such as Z. perennis and Tripsacum dactyloides, are strongly tolerant of cold stress and can thus be used to improve the LTGA of maize. In a previous study, the genetic bridge MTP was constructed (from maize, T. dactyloides, and Z. perennis) and used to obtain a highly LTGA maize introgression line (IB030) by backcross breeding. In this study, IB030 (Strong-LTGA) and Mo17 (Weak-LTGA) were selected as parents to construct an F-2 offspring. Additionally, two major QTLs (qCS1-1 and qCS10-1) were mapped. Then, RNA-seq was performed using seeds of IB030 and the recurrent parent B73 treated at 10 degrees C for 27 days and 25 degrees C for 7 days, respectively, and two candidate genes (ZmbZIP113 and ZmTSAH1) controlling LTGA were located using QTL-seq and integrative transcriptomic analyses. The functional verification results showed that the two candidate genes positively regulated LTGA of IB030. Notably, homologous cloning showed that the source of variation in both candidate genes was the stable inheritance of introgressed alleles from Z. perennis. This study was thus able to analyze the LTGA mechanism of IB030 and identify resistance genes for genetic improvement in maize, and it proved that using MTP genetic bridge confers desirable traits or phenotypes of Z. perennis and tripsacum essential to maize breeding systems.
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