Suppr超能文献

一种用于棉花种子(棉属)无损检测和评估的 DNA 提取方法。

A DNA Extraction Method for Nondestructive Testing and Evaluation of Cotton Seeds (Gossypium L.).

机构信息

Field Crops Department, Faculty of Agriculture, Akdeniz University, 07070, Antalya, Turkey.

Vocational School of Technical Sciences, Akdeniz University, 07070, Antalya, Turkey.

出版信息

Biochem Genet. 2024 Apr;62(2):1347-1364. doi: 10.1007/s10528-023-10496-5. Epub 2023 Aug 21.

Abstract

Kernels of cotton provide lint and linter for textiles, oil and protein for food and feed. Cotton seed is formed following fertilization between an ovule and a pollen grain. The seed coat is maternal in origin, whereas the embryo and attached cotyledonary leaves are hybrids of parental lines. The extraction of genomic DNA from an ungerminated whole, a portion or mixed seeds are prerequisite in genetic and genomic studies of cotton. As far as our knowledge, there is only one method of nondescriptive DNA extraction from ungerminated cotton seeds without affecting the seed germination capability, but it has technical difficulties and requires special equipment. Furthermore, the amount of DNA extracted using the published method is low and, therefore, it is only suitable for routine marker assisted selection studies. In this study, a DNA extraction protocol referred to as the CTAB-LiCl was developed for single whole cotton seed, a portion of cotton seed and bulked cotton seeds. This protocol uses a combination of CTAB and LiCl to lyse cells and deplete RNAs simultaneously. The CTAB-LiCl DNA extraction method was evaluated in ninety-six individuals of six different cotton cultivars along with two genetic standards of cotton, TM-1 (G. hirsutum L.), Pima 3-79 (G. barbadense L.), and several other plant species of different plant genera. Results revealed that this method produced high quality and amounts of DNA as confirmed by spectrophotometry, agarose gel, restriction enzyme digestion, polymerase chain reaction, and library production for next generation sequencing studies of whole genome bisulfite sequencing. It does not require the use of liquid nitrogen, RNase, proteinase K, or beta-mercaptoethanol and can be completed in approximately 2 h. Small tissues of the chalaza ends of ungerminated cotton seeds could be used to obtain high quality and quantity of DNA ranging from 14 to 28 µg without affecting the seeds' germination ability, allowing marker-assisted selection before planting and flowering.

摘要

棉籽的内核为纺织品提供棉绒和麻屑,为食品和饲料提供油和蛋白质。棉花种子是在胚珠和花粉粒受精后形成的。种皮是母体来源的,而胚和附着的子叶是双亲系的杂种。从未发芽的整个种子、部分种子或混合种子中提取基因组 DNA 是棉花遗传和基因组研究的前提。据我们所知,只有一种方法可以在不影响种子发芽能力的情况下从未发芽的棉花种子中提取非描述性 DNA,但该方法存在技术困难,需要特殊设备。此外,使用已发表的方法提取的 DNA 量很低,因此仅适用于常规的标记辅助选择研究。在这项研究中,开发了一种称为 CTAB-LiCl 的 DNA 提取方案,用于单个完整棉花种子、部分棉花种子和混合棉花种子。该方案使用 CTAB 和 LiCl 的组合同时裂解细胞并耗尽 RNA。CTAB-LiCl DNA 提取方法在六个不同棉花品种的九十六个个体以及两个棉花遗传标准品 TM-1(G. hirsutum L.)、Pima 3-79(G. barbadense L.)以及其他几个不同属的植物物种中进行了评估。结果表明,该方法产生了高质量和大量的 DNA,这一点通过分光光度法、琼脂糖凝胶、限制性内切酶消化、聚合酶链反应以及全基因组亚硫酸氢盐测序的下一代测序文库制备得到了证实。它不需要使用液氮、RNase、蛋白酶 K 或β-巯基乙醇,并且可以在大约 2 小时内完成。未发芽的棉籽珠心末端的小组织可以用来获得高质量和数量的 DNA,范围从 14 到 28 µg,而不会影响种子的发芽能力,允许在种植和开花前进行标记辅助选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验