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用于复杂宏基因组长读测序的高分子量 DNA 提取策略。

High molecular weight DNA extraction strategies for long-read sequencing of complex metagenomes.

机构信息

Department of Medicine, The University of Chicago, Chicago, Illinois, USA.

Committee on Microbiology, University of Chicago, Chicago, Illinois, USA.

出版信息

Mol Ecol Resour. 2022 Jul;22(5):1786-1802. doi: 10.1111/1755-0998.13588. Epub 2022 Feb 7.

DOI:10.1111/1755-0998.13588
PMID:35068060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9177515/
Abstract

By offering extremely long contiguous characterization of individual DNA molecules, rapidly emerging long-read sequencing strategies offer comprehensive insights into the organization of genetic information in genomes and metagenomes. However, successful long-read sequencing experiments demand high concentrations of highly purified DNA of high molecular weight (HMW), which limits the utility of established DNA extraction kits designed for short-read sequencing. The challenges associated with input DNA quality intensify further when working with complex environmental samples of low microbial biomass, which requires new protocols that are tailored to study metagenomes with long-read sequencing. Here, we use human tongue scrapings to benchmark six HMW DNA extraction strategies that are based on commercially available kits, phenol-chloroform (PC) extraction and agarose encasement followed by agarase digestion. A typical end goal of HMW DNA extractions is to obtain the longest possible reads during sequencing, which is often achieved by PC extractions, as demonstrated in sequencing of cultured cells. Yet our analyses that consider overall read-size distribution, assembly performance and the number of circularized elements found in sequencing results suggest that column-based kits with enzyme supplementation, rather than PC methods, may be more appropriate for long-read sequencing of metagenomes.

摘要

通过对单个 DNA 分子进行极其长的连续特征描述,新兴的长读测序策略为深入了解基因组和宏基因组中遗传信息的组织提供了全面的见解。然而,成功的长读测序实验需要高浓度的高纯度高分子量(HMW)DNA,这限制了专为短读测序设计的现有 DNA 提取试剂盒的应用。当处理微生物生物量低的复杂环境样本时,输入 DNA 质量的挑战会进一步加剧,这需要新的协议来专门研究使用长读测序的宏基因组。在这里,我们使用人类舌刮取物来对基于商业试剂盒、酚氯仿(PC)提取和琼脂糖包裹后琼脂酶消化的六种 HMW DNA 提取策略进行基准测试。HMW DNA 提取的典型最终目标是在测序过程中获得尽可能长的读长,这通常通过 PC 提取来实现,正如对培养细胞测序所证明的那样。然而,我们的分析考虑了整体读长分布、组装性能以及测序结果中发现的环状元件数量,表明对于宏基因组的长读测序,带有酶补充的柱基试剂盒可能比 PC 方法更合适。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/cf10fef4d304/MEN-22-1786-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/f3974204c43c/MEN-22-1786-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/19d656b5ad23/MEN-22-1786-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/cf10fef4d304/MEN-22-1786-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/f3974204c43c/MEN-22-1786-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/19d656b5ad23/MEN-22-1786-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/642c/9544753/cf10fef4d304/MEN-22-1786-g003.jpg

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