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首页> 外文期刊>Plant Physiology >A Chlorophyll-Deficient Rice Mutant with Impaired Chlorophyllide Esterification in Chlorophyll Biosynthesis
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A Chlorophyll-Deficient Rice Mutant with Impaired Chlorophyllide Esterification in Chlorophyll Biosynthesis

机译:叶绿素生物合成受损的叶绿素缺乏水稻突变体。

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摘要

Chlorophyll (Chl) synthase catalyzes esterification of chlorophyllide to complete the last step of Chl biosynthesis. Although the Chl synthases and the corresponding genes from various organisms have been well characterized, Chl synthase mutants have not yet been reported in higher plants. In this study, a rice (Oryza Sativa) Chl-deficient mutant, yellow-green leaf1 (ygl1), was isolated, which showed yellow-green leaves in young plants with decreased Chl synthesis, increased level of tetrapyrrole intermediates, and delayed chloroplast development. Genetic analysis demonstrated that the phenotype of ygl1 was caused by a recessive mutation in a nuclear gene. The ygl1 locus was mapped to chromosome 5 and isolated by map-based cloning. Sequence analysis revealed that it encodes the Chl synthase and its identity was verified by transgenic complementation. A missense mutation was found in a highly conserved residue of YGL1 in the ygl1 mutant, resulting in reduction of the enzymatic activity. YGL1 is constitutively expressed in all tissues, and its expression is not significantly affected in the ygl1 mutant. Interestingly, the mRNA expression of the cab1R gene encoding the Chl a/b-binding protein was severely suppressed in the ygl1 mutant. Moreover, the expression of some nuclear genes associated with Chl biosynthesis or chloroplast development was also affected in ygl1 seedlings. These results indicate that the expression of nuclear genes encoding various chloroplast proteins might be feedback regulated by the level of Chl or Chl precursors.
机译:叶绿素(Chl)合酶催化叶绿素的酯化反应,以完成Chl生物合成的最后一步。尽管已经很好地表征了Chl合酶和来自各种生物的相应基因,但是尚未在高等植物中报道Chl合酶突变体。在这项研究中,分离出水稻(Oryza Sativa)Chl缺乏突变体黄绿色leaf1(ygl1),该突变株显示年轻植物中的黄绿色叶子具有减少的Chl合成,增加的四吡咯中间体水平和延迟的叶绿体发育。遗传分析表明,ygl1的表型是由核基因的隐性突变引起的。 ygl1基因座被定位到5号染色体,并通过基于图的克隆进行分离。序列分析显示其编码Chl合酶,并且其身份通过转基因互补得到证实。在ygl1突变体中高度保守的YGL1残基中发现了一个错义突变,导致酶活性降低。 YGL1在所有组织中组成性表达,并且在ygl1突变体中其表达未受到明显影响。有趣的是,在ygl1突变体中,编码Chla / b结合蛋白的cab1R基因的mRNA表达被严重抑制。此外,ygl1幼苗中也影响了一些与Chl生物合成或叶绿体发育相关的核基因的表达。这些结果表明,编码各种叶绿体蛋白的核基因的表达可能受Chl或Chl前体水平的反馈调节。

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