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大豆光合作用关键基因的克隆与功能研究

Cloning and functional study of , which is the critical gene of photosynthesis in soybean.

作者信息

Sun Yu Wei, Wang Xin Yu, Liu Lu, Zhang Qi, Xi Yong Jing, Wang Pi Wu

机构信息

JiLin Agricultural University, The Center of Plant Biotechnology, Chang Chun 130118, China.

出版信息

Breed Sci. 2023 Jun;73(3):290-299. doi: 10.1270/jsbbs.23002. Epub 2023 Jun 27.

Abstract

Light provides energy for photosynthesis and is also an important environmental signal that regulates plant growth and development. Ribose-5-phosphate isomerase plays a crucial role in photosynthesis. However, ribose-5-phosphate isomerase has yet to be studied in soybean photosynthesis. To understand the biological function of , in this study, was cloned, plant overexpression vectors and gene editing vectors were successfully constructed, and transformed into recipient soybean JN74 using the Agrobacterium-mediated method. Using qRT-PCR, we analyzed that gene expression was highest in leaves, second highest in roots, and lowest in stems. Promoter analysis revealed the presence of multiple cis-acting elements related to light response in the promoter region of . Compared with the control soybean plants, the net photosynthetic rate and transpiration rate of the overexpression lines were higher than those of the control and gene editing lines, while the intercellular CO concentration was significantly lower than that of the control and gene editing lines; the total chlorophyll, chlorophyll a, chlorophyll b contents and soluble sugar contents of the overexpression plants were significantly higher than those of the recipient and editing plants, indicating that the gene can increase The gene can increase the photosynthetic capacity of soybean plants, providing a theoretical basis and genetic resources for improving soybean yield by regulating photosynthetic efficiency.

摘要

光为光合作用提供能量,也是调节植物生长发育的重要环境信号。5-磷酸核糖异构酶在光合作用中起关键作用。然而,5-磷酸核糖异构酶在大豆光合作用中的研究尚未开展。为了解[具体基因名称未给出]的生物学功能,本研究克隆了[具体基因名称未给出],成功构建了植物过表达载体和基因编辑载体,并通过农杆菌介导法将其转化到受体大豆JN74中。利用qRT-PCR分析发现,[具体基因名称未给出]基因在叶片中表达量最高,在根中次之,在茎中最低。启动子分析表明,[具体基因名称未给出]启动子区域存在多个与光响应相关的顺式作用元件。与对照大豆植株相比,过表达株系的净光合速率和蒸腾速率高于对照和基因编辑株系,而细胞间CO浓度显著低于对照和基因编辑株系;过表达植株的总叶绿素、叶绿素a、叶绿素b含量和可溶性糖含量均显著高于受体和编辑植株,表明[具体基因名称未给出]基因可提高大豆植株的光合能力,为通过调节光合效率提高大豆产量提供了理论依据和遗传资源。

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