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建立用于分析路易波士()基因组的MinION测序和基因组组装程序。

Establishing MinION Sequencing and Genome Assembly Procedures for the Analysis of the Rooibos () Genome.

作者信息

Mgwatyu Yamkela, Cornelissen Stephanie, van Heusden Peter, Stander Allison, Ranketse Mary, Hesse Uljana

机构信息

Department of Biotechnology, University of the Western Cape, Robert Sobukwe Road, Bellville 7535, South Africa.

Agricultural Research Council, Biotechnology Platform, 100 Old Soutpans Road, Onderstepoort 0110, South Africa.

出版信息

Plants (Basel). 2022 Aug 19;11(16):2156. doi: 10.3390/plants11162156.

Abstract

While plant genome analysis is gaining speed worldwide, few plant genomes have been sequenced and analyzed on the African continent. Yet, this information holds the potential to transform diverse industries as it unlocks medicinally and industrially relevant biosynthesis pathways for bioprospecting. Considering that South Africa is home to the highly diverse Cape Floristic Region, local establishment of methods for plant genome analysis is essential. Long-read sequencing is becoming standard procedure for plant genome research, as these reads can span repetitive regions of the DNA, substantially facilitating reassembly of a contiguous genome. With the MinION, Oxford Nanopore offers a cost-efficient sequencing method to generate long reads; however, DNA purification protocols must be adapted for each plant species to generate ultra-pure DNA, essential for these analyses. Here, we describe a cost-effective procedure for the extraction and purification of plant DNA and evaluate diverse genome assembly approaches for the reconstruction of the genome of rooibos (), an endemic South African medicinal plant widely used for tea production. We discuss the pros and cons of nine tested assembly programs, specifically Redbean and NextDenovo, which generated the most contiguous assemblies, and Flye, which produced an assembly closest to the predicted genome size.

摘要

虽然植物基因组分析在全球范围内的进展日益加快,但在非洲大陆,对植物基因组进行测序和分析的却寥寥无几。然而,这些信息有可能改变多个行业,因为它为生物勘探解锁了与医药和工业相关的生物合成途径。鉴于南非是高度多样化的开普植物区系的所在地,在当地建立植物基因组分析方法至关重要。长读长测序正成为植物基因组研究的标准程序,因为这些读长可以跨越DNA的重复区域,极大地促进连续基因组的重新组装。通过MinION,牛津纳米孔公司提供了一种经济高效的测序方法来生成长读长;然而,必须针对每种植物物种调整DNA纯化方案,以生成超纯DNA,这对这些分析至关重要。在这里,我们描述了一种经济高效的植物DNA提取和纯化方法,并评估了多种基因组组装方法,用于重建南非本土药用植物、广泛用于茶叶生产的路易波士茶()的基因组。我们讨论了九个经过测试的组装程序的优缺点,特别是生成了最连续组装的Redbean和NextDenovo,以及生成了最接近预测基因组大小的组装的Flye。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917e/9416007/06cdec9520e1/plants-11-02156-g001.jpg

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