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Mapping and candidate gene analysis for a new top spikelet abortion mutant in rice

机译:水稻新的顶级小穗流产突变体的定位和候选基因分析

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Grain numbers is one of the determinations for rice yield and directly associated with spikelet numbers per panicle and its normal development. Lots of genes responsible for spikelet numbers and spikelet early development have been identified, but the molecular information about the spikelet development at later development is still limited. Here, we isolated a rice spikelet abnormal development mutant, which shows degenerated spikelet at the top panicle and named aborted top spikelet mutant 1(Ats1). The spikelets derived from the middle and bottom branches per panicle of Ats1 show normal development with those of wild type. However, a large number of branches and spikelets with arrested development were often observed only on apex panicle. The abnormality did not appear until the stage In8 when rachises elongate rapidly and reproductive organs get mature, based on observations through SEM analysis. The aborted spikelet could develop the complete floral organs with a pair of rudimentary glume, a pair of empty glume, two lodicule, six stamens and one carpel. But all these floral organs did not develop maturity. Genetic analysis on two F-2 populations indicated that the Ats1 was controlled by a single dominant gene. By using bulked segregant analysis of F-2 population developed from Ats1 crossing with Songjing6, ATS1 was mapped on chromosome 8 between RM3819 and RM5556. Then, the fine mapping was performed with 1078 F-2 population developed from Ats1 and IR36. The ATS1 locus was finely mapped in an 85.7kb region between RM22448 and STS8-2 with 8 genes according to the rice annotation project database. Sequence analysis of the candidate genes within the delimited region of the Ats1 and Akihikari showed two-nucleotide changes, including single-nucleotide substitutions corresponding to an amino acid substitution from asparagine to lysine acid in exons 3 and a 1-bp deletion resulting in a premature stop codon in exon 22 at the candidate gene, LOC_Os08g06480. A cleaved amplified polymorphic sequence (CAPS) marker, CAPS-ats1, was developed from the 1-bp deletion site. The complete cosegregation of the CAPS genotypes with the matching phenotypes were observed in the F-2 populations. This suggested that Os08g06480 is most likely the ATS1 gene. These results will provide more information for better understanding of the molecular mechanism governing top spikelet abortion within a short developmental period.
机译:粒数是水稻产量的决定因素之一,与每穗的小穗数及其正常发育直接相关。已经鉴定出许多导致小穗数量和小穗早期发育的基因,但是关于小穗发育在后期发育的分子信息仍然有限。在这里,我们分离出一个水稻小穗异常发育突变体,该突变体在顶部穗上显示出退化的小穗,并命名为已终止的顶部小穗突变体1(Ats1)。来自Ats1圆锥花序中部和底部分支的小穗显示出与野生型的正常发育。但是,通常仅在先端圆锥花序上观察到大量具有停滞发育的分支和小穗。根据通过SEM分析的观察,直到In8分期时,神经轴突才迅速伸长并且生殖器官成熟,该异常才出现。流产的小穗可以发育完整的花器官,具有一对基本颖片,一对空颖片,两个lo片,六个雄蕊和一个心皮。但是所有这些花器官都没有发育成熟。对两个F-2种群的遗传分析表明,Ats1由单个显性基因控制。通过对来自Ats1与Songjing6杂交的F-2群体进行大量分离分析,将ATS1定位在RM3819和RM5556之间的8号染色体上。然后,用从Ats1和IR36产生的1078个F-2种群进行精细定位。根据水稻注释项目数据库,将ATS1基因座精细定位在RM22448和STS8-2之间的85.7kb区域中,具有8个基因。对Ats1和Akihikari的定界区域内候选基因的序列分析显示出两个核苷酸的变化,包括与外显子3中天冬酰胺到赖氨酸的氨基酸替换相对应的单核苷酸取代和导致早产的1 bp缺失。在第22外显子的候选基因LOC_Os08g06480处终止密码子。从1 bp缺失位点开发了裂解的扩增多态序列(CAPS)标记CAPS-ats1。在F-2人群中观察到CAPS基因型与匹配表型的完全共分离。这表明Os08g06480最有可能是ATS1基因。这些结果将提供更多的信息,以便更好地了解在短的发育期内控制顶部小穗流产的分子机制。

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