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首页> 外文期刊>Plant physiology >Semi-rolled leaf1 encodes a putative glycosylphosphatidylinositol-anchored protein and modulates rice leaf rolling by regulating the formation of bulliform cells
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Semi-rolled leaf1 encodes a putative glycosylphosphatidylinositol-anchored protein and modulates rice leaf rolling by regulating the formation of bulliform cells

机译:半轧制的leaf1编码一种假定的糖基磷脂酰肌醇固定蛋白,并通过调节大疱状细胞的形成来调节稻叶的滚动

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摘要

Leaf rolling is an important agronomic trait in rice (Oryza sativa) breeding and moderate leaf rolling maintains the erectness of leaves and minimizes shadowing between leaves, leading to improved photosynthetic efficiency and grain yields. Although a few rolled-leaf mutants have been identified and some genes controlling leaf rolling have been isolated, the molecular mechanisms of leaf rolling still need to be elucidated. Here we report the isolation and characterization of SEMI-ROLLED LEAF1 (SRL1), a gene involved in the regulation of leaf rolling. Mutants srl1-1 (point mutation) and srl1-2 (transferred DNA insertion) exhibit adaxially rolled leaves due to the increased numbers of bulliform cells at the adaxial cell layers, which could be rescued by complementary expression of SRL1. SRL1 is expressed in various tissues and is expressed at low levels in bulliform cells. SRL1 protein is located at the plasma membrane and predicted to be a putative glycosylphosphatidylinositol-anchored protein. Moreover, analysis of the gene expression profile of cells that will become epidermal cells in wild type but probably bulliform cells in srl1-1 by laser-captured microdissection revealed that the expression of genes encoding vacuolar H ~+-ATPase (subunits A, B, C, and D) and H ~+-pyrophosphatase, which are increased during the formation of bulliform cells, were up-regulated in srl1-1. These results provide the transcript profile of rice leaf cells that will become bulliform cells and demonstrate that SRL1 regulates leaf rolling through inhibiting the formation of bulliform cells by negatively regulating the expression of genes encoding vacuolar H ~+-ATPase subunits and H ~+-pyrophosphatase, which will help to understand the mechanism regulating leaf rolling.
机译:卷叶是水稻育种的重要农艺性状,适度的卷叶可以保持叶片的直立性并使叶片之间的阴影最小化,从而提高了光合效率和谷物产量。尽管已经鉴定出一些卷叶突变体,并且已经分离了一些控制卷叶的基因,但是仍然需要阐明卷叶的分子机制。在这里,我们报告SEMI-ROLLED LEAF1(SRL1)的分离和鉴定,SAF1卷叶的调节基因。突变体srl1-1(点突变)和srl1-2(转移的DNA插入)显示出近端卷曲的叶片,这是由于在近端细胞层上的大疱状细胞数量增加,这可以通过SRL1的互补表达来挽救。 SRL1在各种组织中表达,并在牛状细胞中低水平表达。 SRL1蛋白位于质膜上,预计是推定的糖基磷脂酰肌醇固定蛋白。此外,通过激光捕获显微切割对将在野生型中变成表皮细胞但可能在srl1-1中变成大疱状细胞的细胞的基因表达谱的分析显示,编码液泡H〜+ -ATPase(A,B, C,和D)和H〜+-焦磷酸酶,在大疱状细胞形成过程中增加,在srl1-1中上调。这些结果提供了将成为稻状细胞的水稻叶片细胞的转录本概况,并证明SRL1通过负调控编码液泡H〜+ -ATPase亚基和H〜+焦磷酸酶的基因表达,通过抑制牛状细胞的形成来调节叶片滚动。 ,这将有助于了解调节叶片滚动的机制。

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