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一种适用于作物种子的高质量/高产量长读长测序的DNA提取方法的开发。

Development of a High-Quality/Yield Long-Read Sequencing-Adaptable DNA Extraction Method for Crop Seeds.

作者信息

Shioya Naohiro, Ogiso-Tanaka Eri, Watanabe Masanori, Anai Toyoaki, Hoshino Tomoki

机构信息

Laboratory of Crop Breeding, Graduate School of Agricultural Sciences, Yamagata University, 1-23 Wakaba-Machi, Tsuruoka 997-8555, Yamagata, Japan.

Center for Molecular Biodiversity Research, National Museum of Nature and Science, 4-1-1 Amakubo, Tsukuba 305-0005, Ibaraki, Japan.

出版信息

Plants (Basel). 2023 Aug 17;12(16):2971. doi: 10.3390/plants12162971.

Abstract

Genome sequencing is important for discovering critical genes in crops and improving crop breeding efficiency. Generally, fresh, young leaves are used for DNA extraction from plants. However, seeds, the storage form, are more efficient because they do not require cultivation and can be ground at room temperature. Yet, only a few DNA extraction kits or methods suitable for seeds have been developed to date. In this study, we introduced an improved (IMP) Boom method that is relatively low-cost, simple to operate, and yields high-quality DNA that can withstand long-read sequencing. The method successfully extracted approximately 8 µg of DNA per gram of seed weight from soybean seeds at an average concentration of 48.3 ng/µL, approximately 40-fold higher than that extracted from seeds using a common extraction method kit. The A and A values of the DNA were 1.90 and 2.43, respectively, which exceeded the respective quality thresholds of 1.8 and 2.0. The DNA also had a DNA integrity number value (indicating the degree of DNA degradation) of 8.1, higher than that obtained using the kit and cetyltrimethylammonium bromide methods. Furthermore, the DNA showed a read length N of 20.96 kbp and a maximum read length of 127.8 kbp upon long-read sequencing using the Oxford Nanopore sequencer, with both values being higher than those obtained using the other methods. DNA extracted from seeds using the IMP Boom method showed an increase in the percentage of the nuclear genome with a decrease in the relative ratio of chloroplast DNA. These results suggested that the proposed IMP Boom method can extract high-quality and high-concentration DNA that can be used for long-read sequencing, which cannot be achieved from plant seeds using other conventional DNA extraction methods. The IMP Boom method could also be adapted to crop seeds other than soybeans, such as pea, okra, maize, and sunflower. This improved method is expected to improve the efficiency of various crop-breeding operations, including seed variety determination, testing of genetically modified seeds, and marker-assisted selection.

摘要

基因组测序对于发现作物中的关键基因和提高作物育种效率至关重要。一般来说,新鲜的幼叶用于从植物中提取DNA。然而,种子作为储存形式更高效,因为它们无需种植且可在室温下研磨。然而,迄今为止仅开发了少数适用于种子的DNA提取试剂盒或方法。在本研究中,我们介绍了一种改进的(IMP)Boom方法,该方法成本相对较低、操作简单,并且能产生可耐受长读长测序的高质量DNA。该方法成功从大豆种子中每克种子重量提取了约8μg DNA,平均浓度为48.3ng/μL,比使用普通提取方法试剂盒从种子中提取的量高出约40倍。DNA的A260/A280和A260/A230值分别为1.90和2.43,超过了各自1.8和2.0的质量阈值。该DNA的DNA完整性数值(表明DNA降解程度)为8.1,高于使用试剂盒和十六烷基三甲基溴化铵方法获得的值。此外,使用牛津纳米孔测序仪进行长读长测序时,该DNA的读长N为20.96kbp,最大读长为127.8kbp,这两个值均高于使用其他方法获得的值。使用IMP Boom方法从种子中提取的DNA显示核基因组百分比增加,叶绿体DNA相对比例降低。这些结果表明,所提出的IMP Boom方法可以提取可用于长读长测序的高质量和高浓度DNA,这是其他传统DNA提取方法无法从植物种子中实现的。IMP Boom方法也可适用于除大豆之外的作物种子,如豌豆、秋葵、玉米和向日葵。这种改进的方法有望提高各种作物育种操作的效率,包括种子品种鉴定、转基因种子检测和标记辅助选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e30/10457885/b92cb414b810/plants-12-02971-g001.jpg

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