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利用全基因组重测序技术在与山松甲虫共生的共生真菌长梗长蠕孢菌中发现单核苷酸多态性。

Single-nucleotide polymorphism discovery in Leptographium longiclavatum, a mountain pine beetle-associated symbiotic fungus, using whole-genome resequencing.

机构信息

Department of Forest and Conservation Sciences, University of British Columbia, Vancouver, British Columbia, Canada, V6T 1Z4.

出版信息

Mol Ecol Resour. 2014 Mar;14(2):401-10. doi: 10.1111/1755-0998.12191. Epub 2013 Nov 29.

Abstract

Single-nucleotide polymorphisms (SNPs) are rapidly becoming the standard markers in population genomics studies; however, their use in nonmodel organisms is limited due to the lack of cost-effective approaches to uncover genome-wide variation, and the large number of individuals needed in the screening process to reduce ascertainment bias. To discover SNPs for population genomics studies in the fungal symbionts of the mountain pine beetle (MPB), we developed a road map to discover SNPs and to produce a genotyping platform. We undertook a whole-genome sequencing approach of Leptographium longiclavatum in combination with available genomics resources of another MPB symbiont, Grosmannia clavigera. We sequenced 71 individuals pooled into four groups using the Illumina sequencing technology. We generated between 27 and 30 million reads of 75 bp that resulted in a total of 1, 181 contigs longer than 2 kb and an assembled genome size of 28.9 Mb (N50 = 48 kb, average depth = 125x). A total of 9052 proteins were annotated, and between 9531 and 17,266 SNPs were identified in the four pools. A subset of 206 genes (containing 574 SNPs, 11% false positives) was used to develop a genotyping platform for this species. Using this roadmap, we developed a genotyping assay with a total of 147 SNPs located in 121 genes using the Illumina(®) Sequenom iPLEX Gold. Our preliminary genotyping (success rate = 85%) of 304 individuals from 36 populations supports the utility of this approach for population genomics studies in other MPB fungal symbionts and other fungal nonmodel species.

摘要

单核苷酸多态性(SNPs)正在迅速成为群体基因组学研究的标准标记;然而,由于缺乏经济有效的方法来揭示全基因组变异,以及在筛选过程中需要大量个体来减少确定偏差,因此它们在非模式生物中的应用受到限制。为了在山松甲虫(MPB)的真菌共生体中进行群体基因组学研究发现 SNPs,我们开发了一种发现 SNPs 并制作基因分型平台的路线图。我们采用了 Leptographium longiclavatum 的全基因组测序方法,并结合了另一种 MPB 共生体 Grosmannia clavigera 的现有基因组资源。我们使用 Illumina 测序技术对 71 个个体进行了四组混合测序。我们生成了 27 到 3000 万个 75bp 的读取,总共生成了 1181 个大于 2kb 的 contigs 和一个组装基因组大小为 28.9Mb(N50=48kb,平均深度=125x)。共注释了 9052 个蛋白质,在四个池中共鉴定了 9531 到 17266 个 SNPs。206 个基因(包含 574 个 SNPs,11%的假阳性)的一个子集被用于为该物种开发基因分型平台。使用该路线图,我们使用 Illumina(®)Sequenom iPLEX Gold 开发了总共 147 个 SNP 的基因分型测定,这些 SNP 位于 121 个基因中。我们对来自 36 个种群的 304 个个体的初步基因分型(成功率=85%)支持了该方法在其他 MPB 真菌共生体和其他真菌非模式物种的群体基因组学研究中的应用。

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