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PE-1,编码血红素加氧酶 1,影响水稻(Oryza sativa L.)的抽穗期和叶绿体发育。

PE-1, Encoding Heme Oxygenase 1, Impacts Heading Date and Chloroplast Development in Rice ( Oryza sativa L.).

机构信息

College of Chemistry and Life Sciences , Zhejiang Normal University , Jinhua , Zhejiang 321004 , People's Republic of China.

State Key Laboratory of Rice Biology , China National Rice Research Institute , Hangzhou , Zhejiang 310006 , People's Republic of China.

出版信息

J Agric Food Chem. 2019 Jul 3;67(26):7249-7257. doi: 10.1021/acs.jafc.9b01676. Epub 2019 Jun 21.

DOI:10.1021/acs.jafc.9b01676
PMID:31244201
Abstract

The duration of the rice growth phase has always been an important target trait. The identification of mutations in rice that alter these processes and result in a shorter growth phase could have potential benefits for crop production. In this study, we isolated an early aging rice mutant, pe-1, with light green leaves, using γ-mutated indica rice cultivar and subsequent screening methods, which is known as the phytochrome synthesis factor Se5 that controls rice flowering. The pe-1 plant is accompanied by a decreased chlorophyll content, an enhanced photosynthesis, and a decreased pollen fertility. PE-1, a close homologue of HY1, is localized in the chloroplast. Expression pattern analysis indicated that PE-1 was mainly expressed in roots, stems, leaves, leaf sheaths, and young panicles. The knockout of PE-1 using the CRISPR/Cas9 system decreased the chlorophyll content and downregulated the expression of PE-1-related genes. Furthermore, the chloroplasts of pe-1 were filled with many large-sized starch grains, and the number of osmiophilic granules (a chloroplast lipid reservoir) was significantly decreased. Altogether, our findings suggest that PE-1 functions as a master regulator to mediate in chlorophyll biosynthesis and photosynthetic pathways.

摘要

水稻生长阶段的持续时间一直是一个重要的目标特征。鉴定改变这些过程并导致生长阶段缩短的水稻突变,可能对作物生产有潜在的好处。在这项研究中,我们使用γ诱变籼稻品种和后续的筛选方法,分离出一个早期衰老的水稻突变体 pe-1,其叶片呈淡绿色,该突变体被称为控制水稻开花的光合成色素合成因子 Se5。pe-1 植株伴随着叶绿素含量降低、光合作用增强和花粉育性降低。PE-1 是 HY1 的紧密同源物,定位于叶绿体中。表达模式分析表明,PE-1 主要在根、茎、叶、叶鞘和幼穗中表达。使用 CRISPR/Cas9 系统敲除 PE-1 降低了叶绿素含量,并下调了与 PE-1 相关基因的表达。此外,pe-1 的叶绿体中充满了许多大尺寸的淀粉粒,并且嗜锇颗粒(叶绿体脂质库)的数量显著减少。总之,我们的研究结果表明,PE-1 作为一个主调控因子,调节叶绿素生物合成和光合作用途径。

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