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Characterization and Fine Mapping of a Novel Rice Narrow Leaf Mutant nal9

机译:新型水稻窄叶突变株nal9的鉴定和精细定位

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摘要

A narrow leaf mutant was isolated from transgenic rice (Oryza sativa L.) lines carrying a T-DNA insertion. The mutant is characterized by narrow leaves during its whole growth period, and was named nal9 (narrow leaf 9). The mutant also has other phenotypes, such as light green leaves at the seedling stage, reduced plant height, a small panicle and increased tillering. Genetic analysis revealed that the mutation is controlled by a single recessive gene. A hygromycin resistance assay showed that the mutation was not caused by T-DNA insertion, so a map-based cloning strategy was employed to isolate the nal9 gene. The mutant individuals from the F2 generations of a cross between the nal9 mutant and Longtepu were used for mapping. With 24 F2 mutants, the nal9 gene was preliminarily mapped near the marker RM156 on the chromosome 3. New INDEL markers were then designed based on the sequence differences between japonica and indica at the region near RM156. The nal9 gene was finally located in a 69.3 kb region between the markers V239B and V239G within BAC OJ1212_C05 by chromosome walking. Sequence and expression analysis showed that an ATP-dependent Clp protease proteolytic subunit gene (ClpP) was most likely to be the nal9 gene. Furthermore, the nal9 mutation was rescued by transformation of the ClpP cDNA driven by the 35S promoter. Accordingly, the ClpP gene was identified as the NAL9 gene. Our results provide a basis for functional studies of NAL9 in future work.
机译:从携带T-DNA插入的转基因水稻(Oryza sativa L.)品系中分离出窄叶突变体。该突变体的特征是在其整个生长期中叶片较窄,并命名为nal9(窄叶9)。该突变体还具有其他表型,例如幼苗期的浅绿色叶片,降低的株高,较小的穗数和增加的分till。遗传分析表明,该突变受单个隐性基因控制。潮霉素抗性测定表明该突变不是由T-DNA插入引起的,因此采用了基于图的克隆策略来分离nal9基因。来自nal9突变体和Longtepu之间杂交的F2代的突变体个体用于作图。利用24个F2突变体,将nal9基因初步定位在3号染色体上的标记RM156附近。然后根据粳稻和in稻在RM156附近区域的序列差异设计新的INDEL标记。 nal9基因最终通过染色体行走位于BAC OJ1212_C05中的标记V239B和V239G之间的69.3 kb区域中。序列和表达分析表明,ATP依赖性Clp蛋白酶蛋白水解亚基基因(ClpP)最有可能是nal9基因。此外,通过转化由35S启动子驱动的ClpP cDNA拯救了nal9突变。因此,将ClpP基因鉴定为NAL9基因。我们的结果为将来的NAL9功能研究提供了基础。

著录项

  • 来源
    《植物学报(英文版)》 |2013年第11期|1016-1025|共10页
  • 作者单位

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

    College of Life Sciences, Shanxi Agricultural University, Taigu 030801, China;

    State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou 310006, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2024-01-27 05:47:42
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