以高秆突变体高秆1号为试验材料,常规品种N099为对照,利用酶联免疫法测定突变体种子浸泡24 h后种胚中激素含量。结果表明,高秆1号的3种激素GA3、ZR、IAA的含量均高于对照,其中GA3的含量显著高于对照。杂交F1表现为:GA3含量显著高于两亲...以高秆突变体高秆1号为试验材料,常规品种N099为对照,利用酶联免疫法测定突变体种子浸泡24 h后种胚中激素含量。结果表明,高秆1号的3种激素GA3、ZR、IAA的含量均高于对照,其中GA3的含量显著高于对照。杂交F1表现为:GA3含量显著高于两亲本,但ZR、IAA含量比正常株高亲本还要低。这暗示高秆1号是一种GA3富集型突变体;而与ZR、IAA关联不大。采用陆陆杂交群体对高秆基因进行染色体定位,有4个SSR分子标记与Tp基因连锁,分别是NAU2083、NAU4045、NAU2419和NAU4044,位于Tp基因两侧的分子标记为NAU4045和NAU2419,其遗传距离分别为7.4 c M和41.2 c M。由此,将陆地棉的一个高秆突变体基因Tp定位在棉花Chr.1上。展开更多
Plant height and tillering are crucial factors determining rice plant architecture and influencing rice grain production. In this study, rnulti-tillering dwarf1 （mtdl）, a stable multi-tiller and dwarf mutant, was sc...Plant height and tillering are crucial factors determining rice plant architecture and influencing rice grain production. In this study, rnulti-tillering dwarf1 （mtdl）, a stable multi-tiller and dwarf mutant, was screened from the ethylmethane sulfonate-treated japonica rice variety Wuyunging7. Compared with the wild type, mtdl mutant exhibited pleiotropic phenotypes, including dwarf- ism, more tillers, brittle culms and delayed heading date. By employing map-based cloning strategy, the gene MTD1 was finally mapped to an approximately 66-kb region on the short arm of chromosome 9. Sequencing results showed that the gene LOCOsO9g02650 （BC12） in mtdl mutant had a single nucleotide substitution （G to A）, which gen- erated a premature translation stop. Over-expressing MTD1/BC12 coding sequ（nce rescued all the phenotypes of mtdl mutants including plant height and tillers, which confirms that BC12 is the mutated gene in mtdl mutant. Quantitative reverse tran,-eription-PCR analysis showed that MTDI/BCI2 could negatively regulate the expression of MONOCULM 1, IDEAL PLANT ARCHITECTURE1 and Tillering and Dwarf 1, and control rice tillering. Remark- ably, a-amylase activity analysis and gibberellic acid （GA） treatment showed that the dwarf phenotype of mtdl mutant was dependent on GA biosynthesis pathway. These results facilitated to further uncover the molecular mechanism of the growth and development in rice.展开更多
文摘以高秆突变体高秆1号为试验材料,常规品种N099为对照,利用酶联免疫法测定突变体种子浸泡24 h后种胚中激素含量。结果表明,高秆1号的3种激素GA3、ZR、IAA的含量均高于对照,其中GA3的含量显著高于对照。杂交F1表现为:GA3含量显著高于两亲本,但ZR、IAA含量比正常株高亲本还要低。这暗示高秆1号是一种GA3富集型突变体;而与ZR、IAA关联不大。采用陆陆杂交群体对高秆基因进行染色体定位,有4个SSR分子标记与Tp基因连锁,分别是NAU2083、NAU4045、NAU2419和NAU4044,位于Tp基因两侧的分子标记为NAU4045和NAU2419,其遗传距离分别为7.4 c M和41.2 c M。由此,将陆地棉的一个高秆突变体基因Tp定位在棉花Chr.1上。
基金supported by the National Natural Science Foundation of China (31401464, 31201183)Zhejiang Provincial Natural Science Foundation of China (Y3110194, LY16C130001)+1 种基金China Postdoctoral Science Foundation (2014M561108)the Open Foundation from Zhejiang Provincial Top Key Discipline of Biology (KFJJ2014006)
文摘Plant height and tillering are crucial factors determining rice plant architecture and influencing rice grain production. In this study, rnulti-tillering dwarf1 （mtdl）, a stable multi-tiller and dwarf mutant, was screened from the ethylmethane sulfonate-treated japonica rice variety Wuyunging7. Compared with the wild type, mtdl mutant exhibited pleiotropic phenotypes, including dwarf- ism, more tillers, brittle culms and delayed heading date. By employing map-based cloning strategy, the gene MTD1 was finally mapped to an approximately 66-kb region on the short arm of chromosome 9. Sequencing results showed that the gene LOCOsO9g02650 （BC12） in mtdl mutant had a single nucleotide substitution （G to A）, which gen- erated a premature translation stop. Over-expressing MTD1/BC12 coding sequ（nce rescued all the phenotypes of mtdl mutants including plant height and tillers, which confirms that BC12 is the mutated gene in mtdl mutant. Quantitative reverse tran,-eription-PCR analysis showed that MTDI/BCI2 could negatively regulate the expression of MONOCULM 1, IDEAL PLANT ARCHITECTURE1 and Tillering and Dwarf 1, and control rice tillering. Remark- ably, a-amylase activity analysis and gibberellic acid （GA） treatment showed that the dwarf phenotype of mtdl mutant was dependent on GA biosynthesis pathway. These results facilitated to further uncover the molecular mechanism of the growth and development in rice.
