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通过测序互补克隆大麦坏死3型疾病模拟突变体。

Cloning the barley nec3 disease lesion mimic mutant using complementation by sequencing.

作者信息

Rosignoli Serena, Cosenza Francesco, Moscou Matthew J, Civolani Laura, Musiani Francesco, Forestan Cristian, Milner Sara Giulia, Savojardo Castrense, Tuberosa Roberto, Salvi Silvio

机构信息

Dep. of Agricultural and Food Sciences, Univ. of Bologna, Viale G. Fanin 44, Bologna, Italy, 40127.

The Sainsbury Laboratory, Univ. of East Anglia, Norwich Research Park, Norwich, NR4 7UK, UK.

出版信息

Plant Genome. 2022 Jun;15(2):e20187. doi: 10.1002/tpg2.20187. Epub 2022 Mar 18.

Abstract

Disease lesion mimic (DLM) or necrotic mutants display necrotic lesions in the absence of pathogen infections. They can show improved resistance to some pathogens and their molecular dissection can contribute to revealing components of plant defense pathways. Although forward-genetics strategies to find genes causal to mutant phenotypes are available in crops, these strategies require the production of experimental cross populations, mutagenesis, or gene editing and are time- and resource-consuming or may have to deal with regulated plant materials. In this study, we described a collection of 34 DLM mutants in barley (Hordeum vulgare L.) and applied a novel method called complementation by sequencing (CBS), which enables the identification of the gene responsible for a mutant phenotype given the availability of two or more chemically mutagenized individuals showing the same phenotype. Complementation by sequencing relies on the feasibility to obtain all induced mutations present in chemical mutants and on the low probability that different individuals share the same mutated genes. By CBS, we identified a cytochrome P450 CYP71P1 gene as responsible for orange blotch DLM mutants, including the historical barley nec3 locus. By comparative phylogenetic analysis we showed that CYP71P1 gene family emerged early in angiosperm evolution but has been recurrently lost in some lineages including Arabidopsis thaliana (L.) Heynh. Complementation by sequencing is a straightforward cost-effective approach to clone genes controlling phenotypes in a chemically mutagenized collection. The TILLMore (TM) collection will be instrumental for understanding the molecular basis of DLM phenotypes and to contribute knowledge about mechanisms of host-pathogen interaction.

摘要

疾病病变模拟(DLM)或坏死突变体在没有病原体感染的情况下表现出坏死病变。它们对某些病原体的抗性可能增强,对其进行分子剖析有助于揭示植物防御途径的组成部分。虽然在作物中可以采用正向遗传学策略来寻找导致突变体表型的基因,但这些策略需要构建实验杂交群体、进行诱变或基因编辑,既耗时又耗资源,或者可能需要处理受管制的植物材料。在本研究中,我们描述了一组34个大麦(Hordeum vulgare L.)DLM突变体,并应用了一种名为测序互补(CBS)的新方法,该方法能够在有两个或更多表现相同表型的化学诱变个体的情况下,鉴定出导致突变体表型的基因。测序互补依赖于获取化学突变体中所有诱导突变的可行性,以及不同个体共享相同突变基因的可能性较低。通过CBS,我们鉴定出细胞色素P450 CYP71P1基因是橙色斑点DLM突变体的致病基因,包括历史上的大麦nec3位点。通过比较系统发育分析,我们表明CYP71P1基因家族在被子植物进化早期出现,但在包括拟南芥(Arabidopsis thaliana (L.) Heynh.)在内的一些谱系中反复丢失。测序互补是一种直接且经济高效的方法,用于在化学诱变群体中克隆控制表型的基因。TILLMore(TM)群体将有助于理解DLM表型的分子基础,并为宿主 - 病原体相互作用机制提供知识。

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