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拟南芥 BnaFtsH1 基因在 PSII 修复循环和 FtsH5 缺失中的进化作用

Brassica evolution of essential BnaFtsH1 genes involved in the PSII repair cycle and loss of FtsH5.

机构信息

National Key Laboratory of Crop Genetic Improvement, Hongshan Laboratory, Huazhong Agricultural University, Wuhan, 430070, China.

出版信息

Plant Sci. 2022 Feb;315:111128. doi: 10.1016/j.plantsci.2021.111128. Epub 2021 Nov 23.

Abstract

The PSII repair cycle is an important part of photosynthesis and is essential for high photosynthetic efficiency. The study of essential genes in Brassica napus provides significant potential for the improvement of gene editing technology and molecular breeding design. Previously, we identified a B. napus lethal mutant (7-521Y), which was controlled by two recessive genes (cyd1 and cyd2). BnaC06.FtsH1 was identified as a CYD1 target gene through functional verification. In the present study, we employed fine-mapping, genetic complementation, and CRISPR/Cas9 experiments to identify BnaA07.FtsH1 as the target gene of CYD2, functioning similarly to BnaC06.FtsH1. By analyzing CRISPR/Cas9 T generation plants of the Westar variety, we found that the copy number of FtsH1 was positively correlated with its biomass accumulation. Transcriptome analysis of cotyledons revealed differences in the expression of photosynthesis antenna and structural proteins between the mutant and complementary seedlings. Phylogenetic and chromosome linear analyses, based on 15 sequenced cruciferous species, revealed that Brassica alone had lost FtsH5 during evolution. This may be related to the fact that FtsH5 was located at the end of chromosome ABK8 in the ancestor species. Cloning and identification of BnaFtsH1s provide a deeper understanding of PSII repair cycle mechanisms and offer new insights for the improvement of photosynthetic efficiency and molecular breeding design in B. napus.

摘要

PSII 修复循环是光合作用的重要组成部分,对高光效至关重要。研究甘蓝型油菜必需基因,为基因编辑技术和分子育种设计的改良提供了巨大的潜力。之前,我们鉴定了一个甘蓝型油菜致死突变体(7-521Y),它由两个隐性基因(cyd1 和 cyd2)控制。通过功能验证,鉴定 BnaC06.FtsH1 为 CYD1 的靶基因。本研究采用精细定位、遗传互补和 CRISPR/Cas9 实验,鉴定 BnaA07.FtsH1 为 CYD2 的靶基因,与 BnaC06.FtsH1 功能相似。通过分析 Westar 品种的 CRISPR/Cas9 T 代植株,发现 FtsH1 的拷贝数与其生物量积累呈正相关。对子叶的转录组分析表明,突变体和互补幼苗之间光合作用天线和结构蛋白的表达存在差异。基于 15 个已测序的芸薹属物种的系统发育和染色体线性分析表明,在进化过程中,独甘蓝属失去了 FtsH5。这可能与 FtsH5 位于祖先物种 ABK8 染色体末端有关。BnaFtsH1s 的克隆和鉴定,为 PSII 修复循环机制提供了更深入的了解,并为提高油菜光合作用效率和分子育种设计提供了新的思路。

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