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两个同源基因 YL1 和 YL2 的双突变导致大豆[ Glycine max (L.) Merr]叶片黄化表型。

Double mutation of two homologous genes YL1 and YL2 results in a leaf yellowing phenotype in soybean [Glycine max (L.) Merr].

机构信息

National Center for Soybean Improvement, Key Laboratory of Biology and Genetics and Breeding for Soybean, Ministry of Agriculture, State Key Laboratory for Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing, China.

Shandong Provincial Key Laboratory of Energy Genetics, Key Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, Shandong, China.

出版信息

Plant Mol Biol. 2020 Jul;103(4-5):527-543. doi: 10.1007/s11103-020-01008-9. Epub 2020 Apr 23.

Abstract

Two homologous, chloroplast located CAAX proteases were identified to be functional redundancy in determining soybean leaf color, and they probably play essential roles in regulating light harvesting and absorption during photosynthesis process. Leaf color mutants are ideal materials for studying photosynthesis and chlorophyll metabolism. The soybean [Glycine max (L.) Merr.] yellowing leaf (yl) variation is a recombinant mutant characterized by yellow foliage, which derived from the specific cross between green seed-coated and yellow seed-coated soybean varieties. Molecular cloning and subsequent gene silencing revealed that the yellow leaf trait of yl was controlled by two recessive nuclear genes, glyma11g04660 and glyma01g40650, named as YL1 and YL2 respectively, and the latter was confirmed to be same as the earlier reported green seed-coat gene G. Both YL1 and YL2 belonged to chloroplast-located proteases possessing Abi domain, and these genes were expressed in various tissues, especially in young leaves. In yl, the expression of YL1 and YL2 were suppressed in most tissues, and the young leaf of yl presented an increased maximal photochemical efficiency (Fv/Fm) as well as enhanced net photosynthesis activity (Pn), indicating that YL1 and YL2 are involved in light absorption regulation during photosynthesis process. Collectively, the identification and description of YL1 and YL2 in our study provides insights for the regulatory mechanism of photosynthesis process, and these findings will further assist to clarify the close relationship between photosynthesis and chlorophyll metabolism.

摘要

两种同源的叶绿体定位的 CAAX 蛋白酶被鉴定为在决定大豆叶片颜色方面具有功能冗余性,它们可能在调节光合作用过程中的光吸收和吸收中发挥重要作用。叶片颜色突变体是研究光合作用和叶绿素代谢的理想材料。大豆黄化叶(yl)变异是一种重组突变体,其特征是叶片发黄,它源于绿色种皮和黄色种皮大豆品种之间的特定杂交。分子克隆和随后的基因沉默揭示了 yl 的黄化叶性状由两个隐性核基因 glyma11g04660 和 glyma01g40650 控制,分别命名为 YL1 和 YL2,后者被证实与先前报道的绿色种皮基因 G 相同。YL1 和 YL2 均属于叶绿体定位的蛋白酶,具有 Abi 结构域,这些基因在各种组织中表达,特别是在嫩叶中。在 yl 中,YL1 和 YL2 的表达在大多数组织中受到抑制,yl 的嫩叶表现出增加的最大光化学效率(Fv/Fm)和增强的净光合作用活性(Pn),表明 YL1 和 YL2 参与光合作用过程中的光吸收调节。总之,我们研究中对 YL1 和 YL2 的鉴定和描述为光合作用过程的调节机制提供了新的见解,并进一步阐明了光合作用和叶绿素代谢之间的密切关系。

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