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利用 EMS 诱导的辣椒(Capsicum annuum L.)突变体对低辣味相关位点进行遗传特征分析。

Genetic characterization of a locus responsible for low pungency using EMS-induced mutants in Capsicum annuum L.

机构信息

Department of Agriculture, Forestry and Bioresources, Research Institute of Agriculture and Life Science, Plant Genomics and Breeding Institute, College of Agriculture and Life Science, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

Theor Appl Genet. 2024 Apr 12;137(5):101. doi: 10.1007/s00122-024-04602-3.

Abstract

The pepper mutants ('221-2-1a' and '1559-1-2h') with very low pungency were genetically characterized. The Pun4 locus, responsible for the reduced pungency of the mutant fruits, was localized to a 208 Mb region on chromosome 6. DEMF06G16460, encoding 3-ketoacyl-CoA synthase, was proposed as a strong candidate gene based on the genetic analyses of bulked segregants, DEG, and expression analyses. Capsaicinoids are unique alkaloids present in pepper (Capsicum spp.), synthesized through the condensation of by-products from the phenylpropanoid and branched-chain fatty acid pathways, and accumulating in the placenta. In this study, we characterized two allelic ethyl methanesulfonate-induced mutant lines with extremely low pungency ('221-2-1a' and '1559-1-2h'). These mutants, derived from the pungent Korean landrace 'Yuwolcho,' exhibited lower capsaicinoid content than Yuwolcho but still contained a small amount of capsaicinoid with functional capsaicinoid biosynthetic genes. Genetic crosses between the mutants and Yuwolcho or pungent lines indicated that a single recessive mutation was responsible for the low-pungency phenotype of mutant 221-2-1a; we named the causal locus Pungency 4 (Pun4). To identify Pun4, we combined genome-wide polymorphism analysis and transcriptome analysis with bulked-segregant analysis. We narrowed down the location of Pun4 to a 208-Mb region on chromosome 6 containing five candidate genes, of which DEMF06G16460, encoding a 3-ketoacyl-CoA synthase associated with branched-chain fatty acid biosynthesis, is the most likely candidate for Pun4. The expression of capsaicinoid biosynthetic genes in placental tissues in Yuwolcho and the mutant was consistent with the branched-chain fatty acid pathway playing a pivotal role in the lower pungency observed in the mutant. We also obtained a list of differentially expressed genes in placental tissues between the mutant and Yuwolcho, from which we selected candidate genes using gene co-expression analysis. In summary, we characterized the capsaicinoid biosynthesis-related locus Pun4 through integrated of genetic, genomic, and transcriptome analyses. These findings will contribute to our understanding of capsaicinoid biosynthesis in pepper.

摘要

两个低辣味辣椒突变体('221-2-1a'和'1559-1-2h')的遗传特征被鉴定。负责突变果实低辣味的 Pun4 基因座被定位到 6 号染色体上的 208Mb 区域。基于对混池分离群体、DEG 和表达分析的遗传分析,编码 3-酮酰基辅酶 A 合酶的 DEMF06G16460 被提议为一个强候选基因。辣椒素是辣椒(Capsicum spp.)中特有的生物碱,通过苯丙烷和支链脂肪酸途径的副产物缩合合成,并积累在胎盘中。在这项研究中,我们对两个低辣味的乙基磺酸甲酯诱导突变体('221-2-1a'和'1559-1-2h')进行了特征描述。这些突变体源自辣味韩国地方品种 'Yuwolcho',其辣椒素含量低于 'Yuwolcho',但仍含有少量具有功能性辣椒素生物合成基因的辣椒素。突变体与 'Yuwolcho'或辣味系之间的遗传杂交表明,单个隐性突变是突变体 221-2-1a 低辣味表型的原因;我们将其命名为辣味 4 基因(Pun4)。为了鉴定 Pun4,我们结合了全基因组多态性分析、转录组分析和混池分离群体分析。我们将 Pun4 定位到 6 号染色体上的一个 208Mb 区域,其中包含五个候选基因,其中 DEMF06G16460 编码与支链脂肪酸生物合成相关的 3-酮酰基辅酶 A 合酶,是 Pun4 的最可能候选基因。Yuwolcho 和突变体胎盘中辣椒素生物合成基因的表达与支链脂肪酸途径在突变体中观察到的低辣味中发挥关键作用一致。我们还从突变体和 'Yuwolcho'的胎盘中获得了组织差异表达基因列表,并通过基因共表达分析从中选择候选基因。总之,我们通过遗传、基因组和转录组分析综合鉴定了与辣椒素生物合成相关的 Pun4 基因座。这些发现将有助于我们理解辣椒素在辣椒中的生物合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57b/11014816/9208a5e1a779/122_2024_4602_Fig1_HTML.jpg

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