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在黄瓜(Cucumis sativus L.)中,CsDET2 基因突变导致系统性的油菜素内酯缺乏和超紧凑表型。

A mutant in the CsDET2 gene leads to a systemic brassinosteriod deficiency and super compact phenotype in cucumber (Cucumis sativus L.).

机构信息

College of Horticulture, Northwest A&F University, Yangling, 712100, Shaanxi, China.

Horticulture Department, University of Wisconsin, Madison, WI, 53706, USA.

出版信息

Theor Appl Genet. 2017 Aug;130(8):1693-1703. doi: 10.1007/s00122-017-2919-z. Epub 2017 May 17.

DOI:10.1007/s00122-017-2919-z
PMID:28516384
Abstract

A novel dwarf cucumber mutant, scp-2, displays a typical BR biosynthesis-deficient phenotype, which is due to a mutation in CsDET2 for a steroid 5-alpha-reductase. Brassinosteroids (BRs) are a group of plant hormones that play important roles in the development of plant architecture, and extreme dwarfism is a typical outcome of BR-deficiency. Most cucumber (Cucumis sativus L.) varieties have an indeterminate growth habit, and dwarfism may have its value in manipulation of plant architecture and improve production in certain production systems. In this study, we identified a spontaneous dwarf mutant, super compact-2 (scp-2), that also has dark green, wrinkle leaves. Genetic analyses indicated that scp-2 was different from two previously reported dwarf mutants: compact (cp) and super compact-1 (scp-1). Map-based cloning revealed that the mutant phenotype was due to two single nucleotide polymorphism and a single-base insertion in the CsDET2 gene that resulted in a missense mutation in a conserved amino acid and thus a truncated protein lacking the conserved catalytic domains in the predicted steroid 5α-reductase protein. Measurement of endogenous hormone levels indicated a reduced level of brassinolide (BL, a bioactive BR) in scp-2, and the mutant phenotype could be partially rescued by the application of epibrassinolide (EBR). In addition, scp-2 mutant seedlings exhibited dark-grown de-etiolation, and defects in cell elongation and vascular development. These data support that scp-2 is a BR biosynthesis-deficient mutant, and that the CsDET2 gene plays a key role in BR biosynthesis in cucumber. We also described the systemic BR responses and discussed the specific BR-related phenotypes in cucumber plants.

摘要

一个新的矮生黄瓜突变体,scp-2,表现出典型的 BR 生物合成缺陷表型,这是由于甾体 5α-还原酶的 CsDET2 突变引起的。油菜素内酯(BRs)是一组植物激素,在植物结构发育中起着重要作用,而极端矮化是 BR 缺乏的典型结果。大多数黄瓜(Cucumis sativus L.)品种具有不定型生长习性,矮化在植物结构操纵和提高某些生产系统产量方面可能具有价值。在这项研究中,我们鉴定了一个自发的矮生突变体,超紧凑-2(scp-2),它也具有深绿色、皱纹叶。遗传分析表明,scp-2 与先前报道的两个矮生突变体:紧凑(cp)和超紧凑-1(scp-1)不同。基于图谱的克隆表明,突变表型是由于 CsDET2 基因中的两个单核苷酸多态性和一个单碱基插入导致保守氨基酸的错义突变,从而导致预测的甾体 5α-还原酶蛋白中缺失保守催化结构域的截短蛋白。内源性激素水平的测量表明,scp-2 中的油菜素内酯(BL,一种生物活性 BR)水平降低,施用表油菜素内酯(EBR)可部分挽救突变表型。此外,scp-2 突变体幼苗表现出暗生长去黄化,以及细胞伸长和血管发育缺陷。这些数据支持 scp-2 是一个 BR 生物合成缺陷突变体,CsDET2 基因在黄瓜中 BR 生物合成中起关键作用。我们还描述了系统 BR 反应,并讨论了黄瓜植物中特定的 BR 相关表型。

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Front Plant Sci. 2017 Mar 2;8:266. doi: 10.3389/fpls.2017.00266. eCollection 2017.
2
A Truncated F-Box Protein Confers the Dwarfism in Cucumber.一个截短的F-Box蛋白导致黄瓜矮化。
J Genet Genomics. 2016 Apr 20;43(4):223-6. doi: 10.1016/j.jgg.2016.01.007. Epub 2016 Feb 9.
3
Root proteomics reveals cucumber 24-epibrassinolide responses under Ca(NO3)2 stress.
Theor Appl Genet. 2025 May 19;138(6):120. doi: 10.1007/s00122-025-04909-9.
4
The mutation of ent-kaurenoic acid oxidase, a key enzyme involved in gibberellin biosynthesis, confers a dwarf phenotype to cucumber.内根-贝壳杉烯酸氧化酶是参与赤霉素生物合成的关键酶,该酶的突变赋予黄瓜矮化表型。
Theor Appl Genet. 2024 Dec 24;138(1):12. doi: 10.1007/s00122-024-04785-9.
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Identification and characterization of CsERECTA, a major gene controlling stem elongation through regulating GA biosynthesis in cucumber.鉴定和表征 CsERECTA,一个通过调节黄瓜中 GA 生物合成控制茎伸长的主要基因。
Theor Appl Genet. 2024 Jun 7;137(7):151. doi: 10.1007/s00122-024-04660-7.
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Hortic Res. 2024 Feb 23;11(4):uhae050. doi: 10.1093/hr/uhae050. eCollection 2024 Apr.
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Brassinosteroids-Induced Systemic Stress Tolerance was Associated with Increased Transcripts of Several Defence-Related Genes in the Phloem in Cucumis sativus.油菜素类固醇诱导的系统胁迫耐受性与黄瓜韧皮部中几个防御相关基因的转录本增加有关。
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