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作 者:杨德卫[1] 卢礼斌[1] 程朝平[1] 曾美娟[1] 郑向华[1] 叶宁[1] 刘成德[1] 叶新福[1]
机构地区:[1]福建省农业科学院水稻研究所.福州350018
出 处:《遗传》2012年第8期1064-1072,共9页Hereditas(Beijing)
基 金:福建省自然科学基金项目(编号:2011J01110);福建省农业科学院青年人才创新基金项目(编号:2010QJ-A4);福建省农业科学院科技创新团队建设重点科研项目(编号:CXTD2011-12)资助
摘 要:水稻产量和品质受花器官发育的直接影响,因此对水稻颖花发育机理的研究将有助于水稻产量提高和品质的改良。文章利用60Coγ射线辐照亲本8PW33(籼稻背景)获得一个性状能稳定遗传的内颖退化突变体(编号:MU102),并对其农艺性状和花器官进行了观察和分析。结果显示,相对于野生型,该突变体的株高、每穗总粒数及剑叶宽均显著增加,而结实率则显著降低,差异均达显著水平。解剖镜下观察表明,该突变体内颖退化,外颖弯曲呈现镰刀状,其余器官与野生型表型基本一致。扫描电镜观察显示,突变体与野生型叶片维管束的结构组成以及外颖表皮细胞组成、排列均正常,没有明显差异;与野生型相比,突变体内颖表皮细胞排列较为紧密,推测可能是内颖收缩退化导致的。遗传分析显示该突变性状是由隐性单基因控制,并命名为pd2。利用实验室现有的SSR分子标记将PD2基因定位于水稻第9号染色体上,通过进一步扩大群体和开发新的Indel标记,将PD2基因定位在2个Indel标记之间,两者间的物理距离大约是82 kb。在该物理区间内有一个已经克隆的内颖发育基因REP1,经过测序和比对分析,推测REP1与PD2为等位基因。The yield and quality of rice are directly impacted by floral organ development in rice.Understanding of the floral development mechanism will be useful in genetic improvement of yield and quality.In this study,a rice mutant palea degradation 2(pd2) in an indica cultivar ‘8PW33’ was obtained after 60Co γ-ray treatment.Analysis of the mutant showed that,compared to the wild type,plant height,total grain number per panicle,and sword leaf width were significantly increased,but the seed setting rate were significantly decreased.The florets of the mutant exhibited degraded palea and sickle-shaped tortuous lemma.Detail examination using scanning electron microscopy revealed that when epidermis of the vane and lemma were normal,epidermis of the palea were arranged tightly,which might result from degraded palea.Genetic analysis supported that this mutation phenotype was controlled by a single recessive gene.Polymorphic analysis of simple sequence repeat markers demonstrated that PD2 gene is located on chromosome 9.With a larger mapping population and more indel markers,we further mapped PD2 gene between 2 indel markers with a physical region of about 82 kb.Within this region,there is a cloned gene REP1 known to control rice palea development.By comparing the DNA sequences of REP1 from pd2 and 8PW33,in combination with the results of phenotypic analysis,we concluded that PD2 is an allele of REP1
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