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开发商业黑头鲷()微卫星基因组数据库。

Microsatellite Genome-Wide Database Development for the Commercial Blackhead Seabream ().

机构信息

Institute of Animal Biotechnology, Jilin Academy of Agricultural Sciences, Changchun 130033, China.

Key Laboratory for Sustainable Development of Marine Fisheries, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China.

出版信息

Genes (Basel). 2023 Mar 1;14(3):620. doi: 10.3390/genes14030620.

Abstract

Simple sequence repeats (SSRs), the markers with the highest polymorphism and co-dominance degrees, offer a crucial genetic research resource. Limited SSR markers in blackhead seabream have been reported. The availability of the blackhead seabream genome assembly provided the opportunity to carry out genome-wide identification for all microsatellite markers, and bioinformatic analyses open the way for developing a microsatellite genome-wide database in blackhead seabream. In this study, a total of 412,381 SSRs were identified in the 688.08 Mb genome by Krait software. Whole-genome sequences (10×) of 42 samples were aligned against the reference genome and genotyped using the HipSTR tools by comparing and counting repeat number variation across the SSR loci. A total of 156,086 SSRs with a 2-4 bp repeat were genotyped by HipSTR tools, which accounted for 55.78% of the 2-4 bp SSRs in the reference genome. High accuracy of genotyping was observed by comparing HipSTR tools and PCR amplification. A set of 109,131 loci with a number of alleles ≥ 3 and with a number of genotyped individuals ≥ 6 were reserved to constitute the polymorphic SSR database. Fifty-one polymorphic SSR loci were identified through PCR amplification. This strategy to develop polymorphic SSR markers not only obtained a large set of polymorphic SSRs but also eliminated the need for laborious experimental screening. SSR markers developed in this study may facilitate blackhead seabream research, which lays a certain foundation for further gene tagging and genetic linkage analysis, such as marker-assisted selection, genetic mapping, as well as comparative genomic analysis.

摘要

简单序列重复(SSR)标记具有最高的多态性和共显性程度,是重要的遗传研究资源。黑鲷的 SSR 标记数量有限。黑鲷基因组组装的出现为开展全基因组微卫星标记鉴定提供了机会,生物信息学分析为黑鲷微卫星基因组数据库的开发开辟了道路。本研究利用 Krait 软件在 688.08Mb 基因组中共鉴定到 412381 个 SSR。通过比较和计数 SSR 位点重复数的变化,将 42 个样本的全基因组序列(10×)与参考基因组进行比对,并使用 HipSTR 工具进行基因分型。利用 HipSTR 工具共对 156086 个 2-4 个碱基重复的 SSR 进行了基因分型,占参考基因组中 2-4 个碱基 SSR 的 55.78%。通过比较 HipSTR 工具和 PCR 扩增,观察到基因分型的准确性很高。保留了 109131 个具有 3 个以上等位基因和 6 个以上基因型个体的 SSR 位点,构成多态性 SSR 数据库。通过 PCR 扩增鉴定出 51 个多态性 SSR 位点。这种开发多态性 SSR 标记的策略不仅获得了大量多态性 SSR,而且还省去了费力的实验筛选。本研究开发的 SSR 标记可能有助于黑鲷的研究,为进一步的基因标记和遗传连锁分析(如标记辅助选择、遗传图谱构建以及比较基因组分析)奠定了一定的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41db/10048070/b6685f95dfeb/genes-14-00620-g001.jpg

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