水稻小粒基因SG101的鉴定和精细定位
收稿日期: 2017-11-05
修回日期: 2017-04-03
网络出版日期: 2017-11-10
基金资助
国家自然科学基金资助项目(91435105, 91735303, 31661143006);中国农业科学院科技创新工程资助项目
Identification and Fine Mapping of Small Grain Gene SG101 in Rice (Oryza sativa L.)
Received date: 2017-11-05
Revised date: 2017-04-03
Online published: 2017-11-10
【目的】 籽粒大小是决定水稻产量的重要农艺性状之一,开展水稻籽粒大小相关基因的克隆和功能研究对于阐述水稻产量形成的遗传调控机制具有重要意义。【方法】 利用甲基磺酸乙酯诱变粳稻品种中花11,筛选获得一小粒突变体,命名为sg101(small grain 101)。通过形态学、细胞学手段调查了SG101的突变对籽粒大小、穗部主要性状及颖壳细胞数目和大小的影响,通过测定叶夹角和胚芽鞘长度分析其对外施油菜素内酯的差异响应,结合定量PCR技术分析了油菜素内酯合成途径和信号途径相关基因表达情况,并利用图位克隆的手段精细定位了水稻小粒基因SG101。【结果】 与野生型相比,突变体sg101粒长和粒宽均极显著减小,从而导致千粒重极显著降低。此外,sg101还表现出结实率降低、穗长变短、二次枝梗数减少、植株变矮等。细胞学观察发现sg101的颖壳细胞大小没有改变,但细胞数目明显减少。定量PCR检测表明sg101中的细胞周期相关基因表达显著下降。另外,突变体sg101对外施油菜素内酯响应迟钝,其油菜素内酯合成途径和信号途径相关基因表达亦显著降低。【结论】 遗传分析表明sg101突变体由隐性单基因控制,通过图位克隆的方法将SG101精细定位于第1染色体上,物理距离为265 kb的区间内。这为该基因的克隆及深入的功能研究奠定了基础。
汪玉琼, 杨窑龙, 冷语佳, 黄李超, 陈龙, 代丽萍, 涂政军, 高易宏, 胡江, 朱丽, 张光恒, 任德勇, 高振宇, 董国军, 陈光, 郭龙彪, 叶国友, 钱前, 曾大力 . 水稻小粒基因SG101的鉴定和精细定位[J]. 中国水稻科学, 2017 , 31(6) : 580 -589 . DOI: 10.16819/j.1001-7216.2017.6152
【Objective】Grain size is an important agronomic trait in determining grain yield. The characterization and identification of grain size related genes will be beneficial to expound the genetic regulatory mechanisms behind yield formation in rice. 【Method】Here, we report the characterization of a rice (Oryza sativa L.) mutant, small grain 101 (sg101), gained by EMS mutagenesis for Zhonghua 11. The effects of sg101 on grain size, panicle-related traits, cell number and size of lemma were assessed by morphological and cytological methods. The responses to brassinolide(BR) were detected based on the variation in leaf angle and coleoptile length. The expression level of BR signal and synthesis related genes were tested by RT-PCR. Map-based cloning was executed for fine mapping of SG101.【Result】The grain length, grain width and grain weight were significantly reduced in sg101. Moreover, sg101 showed decreased panicle length, secondary rachis branch number, plant height and seed setting rate. The paraffin section observation under a scanning electron microscope indicated that the cell number in sg101 was significantly decreased, while the cell size was similar to wild type, suggesting that SG101 affected the grain size by regulating the cell division. Quantitative RT-PCR analysis displayed that the expression of cell cycle related genes was reduced in sg101. After treatment with BR, sg101 showed smaller leaf angle and shorter coleoptile than those of the wild type and the expression of BR biosynthetic and signal pathway related genes was down-regulated in sg101. Genetic analysis revealed that sg101 phenotype was controlled by a single recessive nuclear gene.【Conclusion】SG101 was mapped on the long arm of chromosome 1 between two STS markers S5 and S6 with a 265 kb physical distance. It laid a base for the further cloning and functional analysis of SG101.
Key words： rice; small grain; sg101; brassinolide
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