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葡萄体细胞无性系(Vitis vinifera L.)DNA甲基化模式的变异

Variation in DNA methylation patterns of grapevine somaclones (Vitis vinifera L.).

作者信息

Schellenbaum Paul, Mohler Volker, Wenzel Gerhard, Walter Bernard

机构信息

Université de Haute Alsace, Laboratoire Vigne Biotechnologies & Environnement, 33 rue de Herrlisheim, BP 50568, F-68008 Colmar, France.

出版信息

BMC Plant Biol. 2008 Jul 15;8:78. doi: 10.1186/1471-2229-8-78.

Abstract

BACKGROUND

In traditional vine areas, the production should present a typicity that partly depends on the grapevine variety. Therefore, vine improvement is considered difficult because of the limited choice in the natural variability of the cultivars within the limits of their characteristics. A possibility to circumvent this problem is the use of somatic variability. In vitro somatic embryogenesis and organogenesis can lead to genotypic and phenotypic variations, described as somaclonal variation, that could be useful for the selection of improved grapevine genotypes.

RESULTS

In order to study tissue culture-induced variation of grapevine, we have analysed 78 somaclones obtained from somatic embryos of two distinct cultivars using molecular marker techniques. SSRs were only useful to verify the conservation of the microsatellite genotype between the somaclones and the respective mother clones. AFLP polymorphism between mother clones and somaclones was 1.3-2.8 times higher to that found between clones. However, a majority of the somaclones (45/78) exhibited only few changes. Seven and five somaclones of 'Chardonnay 96' and 'Syrah 174', respectively, which covered at least all polymorphic loci found in AFLP analysis were used for MSAP study. All of the 120 polymorphic fragments were found only in the somaclones. The percentage of full methylation at CCGG recognition sites was slightly higher in somaclones due to more polymorphic bands generated after cleavage by EcoRI/HpaII. Different digestion patterns revealed different methylation status, especially different levels of de-methylation, that are the consequence of the in vitro culture.

CONCLUSION

MSAP highlights DNA methylation variation in somaclones compared to mother clones and, therefore, is a powerful tool for genotypic characterisation of somatic embryo-derived grapevines. The detection of the same polymorphic bands in numerous somaclones of different cultivars suggests the possibility of hot spots of DNA methylation variation. SSR profiles of the 'Chardonnay' and 'Syrah' somaclones were the same as of the respective mother clones. The somaclones exhibited a higher AFLP variation than clones obtained via traditional clonal selection in the field. Therefore, somatic embryogenesis through in vitro culture technique could be useful for the selection of improved cultivars with subtle changes but conserving their main characteristics.

摘要

背景

在传统葡萄园产区,葡萄酒的生产应展现出一定的典型性,这部分取决于葡萄品种。因此,由于在品种特征范围内自然变异的选择有限,葡萄改良被认为具有难度。解决这一问题的一种可能方法是利用体细胞变异。体外体细胞胚胎发生和器官发生可导致基因型和表型变异,即体细胞克隆变异,这可能有助于筛选改良的葡萄基因型。

结果

为了研究组织培养诱导的葡萄变异,我们使用分子标记技术分析了从两个不同品种的体细胞胚获得的78个体细胞克隆。简单序列重复(SSRs)仅有助于验证体细胞克隆与其各自母本克隆之间微卫星基因型的保守性。母本克隆与体细胞克隆之间的扩增片段长度多态性(AFLP)多态性比克隆之间高1.3 - 2.8倍。然而,大多数体细胞克隆(45/78)仅表现出很少的变化。分别选取了‘霞多丽96’的7个和‘西拉174’的5个体细胞克隆用于甲基化敏感扩增多态性(MSAP)研究,这些克隆至少覆盖了AFLP分析中发现的所有多态位点。所有120个多态性片段仅在体细胞克隆中发现。由于经EcoRI/HpaII酶切后产生更多多态性条带,体细胞克隆中CCGG识别位点的完全甲基化百分比略高。不同的酶切模式揭示了不同的甲基化状态,尤其是不同程度的去甲基化,这是体外培养的结果。

结论

与母本克隆相比,MSAP突出了体细胞克隆中的DNA甲基化变异,因此是用于体细胞胚来源葡萄基因型鉴定的有力工具。在不同品种的众多体细胞克隆中检测到相同的多态性条带,表明存在DNA甲基化变异热点的可能性。‘霞多丽’和‘西拉’体细胞克隆的SSRs图谱与各自母本克隆相同。体细胞克隆表现出比通过田间传统克隆选择获得的克隆更高的AFLP变异。因此,通过体外培养技术进行体细胞胚胎发生可能有助于筛选具有细微变化但保留其主要特征的改良品种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b7b/2491626/95f37e2ee77f/1471-2229-8-78-1.jpg

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