Yang De Wei, Zheng Xiang Hua, Cheng Chao Ping, Ye Ning, Huang Feng Huang, Ye Xin Fu
Institute of Rice, Fujian Academy of Agricultural Sciences, Fuzhou 350018, China.
Yi Chuan. 2018 Dec 20;40(12):1101-1111. doi: 10.16288/j.yczz.18-044.
Rice is an important food crop in the world. The awn may protect rice seeds from being cut by birds, which is important in rice domestication, survival and diffusion. However, the characteristic of awn is gradually washed out during rice domestication and artificial selection. Mapping and cloning of rice awn genes is the basis of studying the genetic mechanism of awn domestication. In this study, 146 chromosome segment substitution lines (CSSLs) derived from DongNanHui 810/ZhangPu wild rice with DongNanHui 810 as the recurrent parent were used to analyze the quantitative trait loci (QTL) controlling the long awn of rice. The results showed that four CSSLs contained one QTL for the long awn. Using substitution mapping, the GAD1-2 gene was mapped between two markers (Ind8-10 and RM4936) on chromosome 8, with a genetic distance of about 4.75 Mb. Using the dominant individuals of segregating populations, the GAD1-2 gene was eventually located between two Indel markers, with a physical distance of about 27 kb, which contained only two candidate genes Os08g0485500 and Os08g0485400. Sequencing analysis showed that Os08g0485500 was the candidate gene of GAD1-2. Further analysis showed that there were six bases missing in the conservative ORF region, resulting in the absence of serine and cysteine that led to the long awn of the four CSSLs. The GAD1 gene was also cloned in this position, suggesting that GAD1-2 and GAD1 were allelic. This study laid a foundation for further understanding of the genetic regulation mechanism and genetic evolution of the awn gene in rice.
水稻是世界上重要的粮食作物。芒可能保护水稻种子不被鸟类啄食,这在水稻驯化、生存和传播过程中具有重要意义。然而,在水稻驯化和人工选择过程中,芒的特性逐渐消失。水稻芒基因的定位与克隆是研究芒驯化遗传机制的基础。本研究以东南辉810为轮回亲本,利用东南辉810/漳浦野生稻衍生的146个染色体片段代换系(CSSLs)分析控制水稻长芒性状的数量性状位点(QTL)。结果表明,4个CSSLs中各含有1个控制长芒的QTL。通过代换作图,将GAD1-2基因定位在第8染色体上的两个标记(Ind8-10和RM4936)之间,遗传距离约为4.75 Mb。利用分离群体中的显性个体,最终将GAD1-2基因定位在两个Indel标记之间,物理距离约为27 kb,该区间仅包含两个候选基因Os08g0485500和Os08g0485400。测序分析表明,Os08g0485500是GAD1-2的候选基因。进一步分析发现,保守的开放阅读框(ORF)区域有6个碱基缺失,导致4个CSSLs中丝氨酸和半胱氨酸缺失,从而形成长芒。在此位置也克隆到了GAD1基因,表明GAD1-2与GAD1是等位基因。本研究为进一步了解水稻芒基因的遗传调控机制和遗传进化奠定了基础。