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首页> 外文期刊>Molecular Breeding >Candidate gene prediction for a petal degeneration mutant, pdm, of the Chinese cabbage (Brassica campestris ssp pekinensis) by using fine mapping and transcriptome analysis
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Candidate gene prediction for a petal degeneration mutant, pdm, of the Chinese cabbage (Brassica campestris ssp pekinensis) by using fine mapping and transcriptome analysis

机译:候选基因预测瓣膜变性突变体,PDM,大白菜(Brassica Campestris SSP Pekinensis)使用细映射和转录组分析

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摘要

A stably inherited petal degeneration mutant pdm of the Chinese cabbage was obtained from its wild-type 'FT' by radiation treatment (Co-60 gamma-rays) and isolated microspore culture. Petals of the pdm mutant were observed to be shriveled, degenerated, not fully expanded, and darker at the flowering stage than those of 'FT.' The pdm mutant phenotype was found to be controlled by a single recessive nuclear gene. For linkage analysis and gene mapping, 1419 recessive homozygous individuals with the pdm phenotype of the F-2 generation were investigated as the mapping population. Results showed that the pdm was located between markers Indelhsn26 and SSRhsn123 at a genetic distance of 0.04 and 0.04 cM, respectively, on linkage group A01. Physical distance between Indelhsn26 and SSRhsn123, the two most closely linked markers, was estimated to be approximately 285.2 kb. Twenty-eight genes were predicted in the target region. Using RNA-seq, Bra040093 was predicted to be the most likely candidate gene for pdm. Based on gene annotation, Bra040093 encodes a peroxisomal acyl-coenzyme A oxidase 1 (ACX1). Comparison of the sequences in pdm and 'FT' revealed two single-nucleotide polymorphisms in pdm. Expression patterns of Bra040093 between pdm and 'FT' were analyzed using quantitative real-time PCR, and the expression level was dramatically higher in 'FT' than in pdm. These findings provide a solid foundation and valuable resources for map-based cloning, identification, and functional analysis of pdm and facilitate the understanding of floral development processes in the Chinese cabbage.
机译:通过辐射处理(CO-60γ射线)和分离的微孔培养,从其野生型'ft'获得了稳定遗传的花瓣退化突变体PDM。观察到PDM突变体的花瓣萎缩,退化,没有完全扩张,并且在开花阶段比'ft'更暗。发现PDM突变表型被单一隐性核基因控制。对于连杆分析和基因测绘,研究了具有F-2代的PDM表型的1419个隐性纯合体作为绘图群体。结果表明,PDM分别位于标记IndelHSN26和SSRHSN123之间,分别在连杆组AO1上的遗传距离为0.04和0.04厘米。 IndelHSN26和SSRHSN123之间的物理距离,两个最紧密的链接标记,估计约为285.2 KB。目标区域预测了二十八个基因。使用RNA-SEQ,预计BRA040093是最可能的PDM候选基因。基于基因注释,BRA040093编码过氧异相亚酰基辅酶A氧化酶1(ACX1)。 PDM和'FT'中序列的比较显示了PDM中的两种单核苷酸多态性。使用定量实时PCR分析PDM和'FT'之间的Bra040093的表达模式,表达水平在“FT”中显着高于PDM。这些调查结果为PDM的地图克隆,鉴定和功能分析提供了坚实的基础和有价值的资源,并促进了大白菜中的花卉开发过程的理解。

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  • 来源
    《Molecular Breeding》 |2016年第3期|共10页
  • 作者单位

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

    Shenyang Agr Univ Dept Hort 120 Dongling Rd Shenyang 110866 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物学;
  • 关键词

    Chinese cabbage; Petal degeneration mutant; Genetic characterization; SSR and Indel markers; Fine mapping;

    机译:大白菜;瓣变性突变体;遗传表征;SSR和indel标记;精细映射;

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