Guo Zhenhua, Cai Lijun, Chen Zhiqiang, Wang Ruiying, Zhang Lanming, Guan Shiwu, Zhang Shuhua, Ma Wendong, Liu Chuanxue, Pan Guojun
Rice Research Institute of Heilongjiang Academy of Agricultural Sciences, Jiamusi 154026, People's Republic of China.
National Engineering Research Center of Plant Space Breeding, South China Agricultural University, Guangzhou 510642, People's Republic of China.
R Soc Open Sci. 2020 Nov 18;7(11):201081. doi: 10.1098/rsos.201081. eCollection 2020 Nov.
Rice is sensitive to low temperatures, specifically at the booting stage. Chilling tolerance of rice is a quantitative trait loci that is governed by multiple genes, and thus, its precise identification through the conventional methods is an arduous task. In this study, we investigated the candidate genes related to chilling tolerance at the booting stage of rice. The F2 population was derived from Longjing25 (chilling-tolerant) and Longjing11 (chilling-sensitive) cross. Two bulked segregant analysis pools were constructed. A 0.82 Mb region containing 98 annotated genes on chromosomes 6 and 9 was recognized as the candidate region associated with chilling tolerance of rice at the booting stage. Transcriptomic analysis of Longjing25 and Longjing11 revealed 50 differentially expressed genes (DEGs) on the candidate intervals. KEGG pathway enrichment analysis of DEGs was performed. Nine pathways were found to be enriched, which contained 10 DEGs. A total of four genes had different expression patterns or levels between Longjing25 and Longjing11. Four out of the 10 DEGs were considered as potential candidate genes for chilling tolerance. This study will assist in the cloning of the candidate genes responsible for chilling tolerance and molecular breeding of rice for the development of chilling-tolerant rice varieties.
水稻对低温敏感,尤其是在孕穗期。水稻的耐冷性是一个由多个基因控制的数量性状位点,因此,通过传统方法精确鉴定它是一项艰巨的任务。在本研究中,我们调查了与水稻孕穗期耐冷性相关的候选基因。F2群体来源于龙井25(耐冷)和龙井11(冷敏感)的杂交。构建了两个混合分离群体分析池。一个位于第6和9号染色体上、包含98个注释基因的0.82 Mb区域被确定为与水稻孕穗期耐冷性相关的候选区域。对龙井25和龙井11进行转录组分析,在候选区间发现了50个差异表达基因(DEG)。对DEG进行了KEGG通路富集分析。发现有9条通路富集,其中包含10个DEG。在龙井25和龙井11之间,共有4个基因具有不同的表达模式或水平。10个DEG中的4个被认为是耐冷性的潜在候选基因。本研究将有助于克隆负责耐冷性的候选基因,并为培育耐冷水稻品种进行水稻分子育种。