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深绿颖 1 抑制金黄质活性,从而减少水稻颖壳中的叶绿素合成。

DEEP GREEN PANICLE1 suppresses GOLDEN2-LIKE activity to reduce chlorophyll synthesis in rice glumes.

机构信息

Key Laboratory of Plant Functional Genomics of the Ministry of Education/Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding/Jiangsu Key Laboratory of Crop Genetics and Physiology, College of Agriculture, Yangzhou University, Yangzhou 225009, China.

Jiangsu Co-Innovation Center for Modern Production Technology of Grain Crops, Yangzhou University, Yangzhou 225009, China.

出版信息

Plant Physiol. 2021 Mar 15;185(2):469-477. doi: 10.1093/plphys/kiaa038.

Abstract

Understanding the regulation mechanisms of photosynthesis is key to improving its efficiency and, ultimately, crop yield. In this study, we report that DEEP GREEN PANICLE1 (DGP1) is involved in photosynthesis regulation in rice (Oryza sativa L.). We identified the dgp1 mutant, which has increased chlorophyll content in glumes. The mutated gene was isolated by map-based cloning. Knockout plants, generated using a gene editing approach, mimic the phenotype of dgp1. Overexpression of DGP1 leads to chlorotic leaves and glumes. DGP1 is a plant-specific protein with a conserved TIGR01589 domain. The expression of DGP1 was detected in green tissues and is induced by light. Moreover, genes involved in key steps of chlorophyll synthesis are upregulated in the glumes of dgp1. Importantly, we found that DGP1 interacts with the rice proteins GOLDEN2-LIKE1 (OsGLK1) and GOLDEN2-LIKE2 (OsGLK2), the two transcription factors involved in the regulation of photosynthesis. Transactivation assays showed that DGP1 represses the activation activity of OsGLK1 on its target genes. Our results demonstrate that DGP1 is a repressor of OsGLK activity and thus photosynthesis in rice. Manipulation of this gene and its homologs in other crops may provide new approaches for high photosynthetic efficiency breeding.

摘要

理解光合作用的调控机制是提高其效率并最终提高作物产量的关键。在这项研究中,我们报告了 DEEP GREEN PANICLE1(DGP1)参与水稻(Oryza sativa L.)光合作用的调控。我们鉴定了 dgp1 突变体,其颖壳中的叶绿素含量增加。通过基于图谱的克隆分离出突变基因。使用基因编辑方法生成的敲除植物模拟了 dgp1 的表型。DGP1 的过表达导致叶片和颖壳呈黄化。DGP1 是一种具有保守 TIGR01589 结构域的植物特异性蛋白。DGP1 的表达在绿色组织中检测到,并受光诱导。此外,在 dgp1 的颖壳中,参与叶绿素合成关键步骤的基因上调。重要的是,我们发现 DGP1 与水稻蛋白 GOLDEN2-LIKE1(OsGLK1)和 GOLDEN2-LIKE2(OsGLK2)相互作用,这两个转录因子参与光合作用的调控。转录激活测定表明 DGP1 抑制 OsGLK1 对其靶基因的激活活性。我们的结果表明,DGP1 是 OsGLK 活性的抑制剂,因此也是水稻光合作用的抑制剂。操纵该基因及其在其他作物中的同源物可能为高光合效率育种提供新方法。

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