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用于……的EST-SSR标记的开发与特性分析 (原文不完整,此为根据现有内容尽量完整的翻译)

Development and characterization of EST-SSR markers for .

作者信息

Tong Yan, Gao Li-Zhi

机构信息

Yunnan Key Laboratory for Wild Plant Resources Kunming Institute of Botany Chinese Academy of Sciences 132 Lanhei Road Kunming 650201 Yunnan China.

Germplasm Bank of Wild Species Kunming Institute of Botany Chinese Academy of Sciences 132 Lanhei Road Kunming 650201 Yunnan China.

出版信息

Appl Plant Sci. 2020 May 22;8(5):e11348. doi: 10.1002/aps3.11348. eCollection 2020 May.

Abstract

PREMISE

, which is native to southwestern China, is an economically important plant belonging to the family Theaceae. We developed expressed sequence tag-simple sequence repeat (EST-SSR) markers for , which can be used to investigate its genetic diversity, population structure, and evolutionary history.

METHODS AND RESULTS

We detected 4780 SSRs in from RNA-Seq data deposited in the National Center for Biotechnology Information's expressed sequence tags database (dbEST). Primer pairs for 70 SSR loci were designed and used for PCR amplification using 90 individuals from four populations of . Of these loci, 50 microsatellite markers were successfully identified, including 11 polymorphic markers. The allele number per locus ranged from two to seven (mean = 4.182), and the levels of observed and expected heterozygosity ranged from 0.044 to 0.567 and from 0.166 to 0.642, respectively. Eleven primer pairs amplified PCR products in three other species of (, , and ).

CONCLUSIONS

The set of microsatellite markers developed here can be used to study the genetic variation and population structure of and related species and thereby help to develop conservation strategies for this species.

摘要

前提

原产于中国西南部的[植物名称]是山茶科一种具有重要经济价值的植物。我们开发了[植物名称]的表达序列标签 - 简单序列重复(EST - SSR)标记,可用于研究其遗传多样性、种群结构和进化历史。

方法与结果

我们从美国国立生物技术信息中心的表达序列标签数据库(dbEST)中存储的[植物名称]RNA - Seq数据中检测到4780个SSR。设计了70个SSR位点的引物对,并用于对来自[植物名称]四个种群的90个个体进行PCR扩增。在这些位点中,成功鉴定出50个微卫星标记,包括11个多态性标记。每个位点的等位基因数范围为2至7(平均值 = 4.182),观察到的杂合度和预期杂合度水平分别为0.044至0.567和0.166至0.642。11对引物在[植物名称]的其他三个物种([物种1名称]、[物种2名称]和[物种3名称])中扩增出了PCR产物。

结论

这里开发的微卫星标记集可用于研究[植物名称]及其相关物种的遗传变异和种群结构,从而有助于制定该物种的保护策略。

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本文引用的文献

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CAP3: A DNA sequence assembly program.CAP3:一个DNA序列组装程序。
Genome Res. 1999 Sep;9(9):868-77. doi: 10.1101/gr.9.9.868.

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