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改良低盐 CTAB 法从富含杂质的组织中提取高质量 DNA。

Modified low-salt CTAB extraction of high-quality DNA from contaminant-rich tissues.

机构信息

Department of Fisheries and Oceans Canada, Gulf Fisheries Center, 343 Universite Avenue, Moncton, NB, E1C 9B6, Canada.

出版信息

Mol Ecol Resour. 2017 Jul;17(4):686-693. doi: 10.1111/1755-0998.12616. Epub 2016 Nov 18.

Abstract

The increasing use of high-throughput sequencing platforms has made the isolation of pure, high molecular weight DNA a primary concern for studies of a diverse range of organisms. Purification of DNA remains a significant challenge in many tissue and sample types due to various organic and inorganic molecules that coprecipitate with nucleic acids. Molluscs, for example, contain high concentrations of polysaccharides which often coprecipitate with DNA and can inhibit downstream enzymatic reactions. We modified a low-salt CTAB (MoLSC) extraction protocol to accommodate contaminant-rich animal tissues and compared this method to a standard CTAB extraction protocol and two commercially available animal tissue DNA extraction kits using oyster adductor muscle. Comparisons of purity and molecular integrity showed that our in-house protocol yielded genomic DNA generally free of contaminants and shearing, whereas the traditional CTAB method and some of the commercial kits yielded DNA unsuitable for some applications of massively parallel sequencing. Our open-source MoLSC protocol provides a cost-effective, scalable, alternative DNA extraction method that can be easily optimized and adapted for sequencing applications in other contaminant-rich samples.

摘要

高通量测序平台的广泛应用使得从各种生物体中分离出纯的高分子量 DNA 成为首要关注的问题。由于与核酸共沉淀的各种有机和无机分子,许多组织和样本类型的 DNA 纯化仍然是一个重大挑战。例如,软体动物中含有高浓度的多糖,这些多糖通常与 DNA 共沉淀,并可能抑制下游的酶反应。我们对低盐 CTAB(MoLSC)提取方案进行了修改,以适应富含污染物的动物组织,并使用牡蛎闭壳肌比较了这种方法与标准 CTAB 提取方案和两种市售的动物组织 DNA 提取试剂盒。对纯度和分子完整性的比较表明,我们的内部方案通常可以得到不含污染物和剪切的基因组 DNA,而传统的 CTAB 方法和一些商业试剂盒得到的 DNA 不适用于大规模平行测序的某些应用。我们的开源 MoLSC 方案提供了一种经济高效、可扩展的替代 DNA 提取方法,可以轻松地针对其他富含污染物的样品的测序应用进行优化和调整。

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