• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于 RAD-seq 技术的中国大型溞种群 SSR 标记开发及遗传多样性分析。

Development of SSR markers and genetic diversity analysis based on RAD-seq technology among Chinese populations of Daphnia magna.

机构信息

School of Environment and Chemical Engineering, Shanghai University, Shanghai, 200444, China.

College of Marine Ecology and Environment, Shanghai Ocean University, Shanghai, 201306, China.

出版信息

Mol Biol Rep. 2022 Jun;49(6):4389-4397. doi: 10.1007/s11033-022-07274-8. Epub 2022 May 12.

DOI:10.1007/s11033-022-07274-8
PMID:35552958
Abstract

BACKGROUND

Daphnia magna belongs to the Cladocera order and plays an important role in the aquatic ecosystem. With the intensification of water pollution, the wild population of D. magna has declined rapidly in recent years, and insufficient molecular markers have limited effective research and conservation of this species.

METHODS AND RESULTS

26 novel microsatellite (SSR) markers were developed in an artificially domesticated D. magna and 12 wild D. magna populations using restriction site-associated DNA sequencing (RAD-seq). The results showed that the observed heterozygosity (Ho) and expected heterozygosity (He) ranged from 0.083 to 0.999 and 0.085 to 0.862, respectively. The PIC ranged from 0.368 to 0.805. These results indicate that the developed SSR marker is highly polymorphic. Nei's genetic identity (H) ranged from 0.0926 to 0.3462. Shannon's Information index (I) ranged from 0.1333 to 0.4799. Genetic distance and Nei's genetic identity analysis, NJ tree diagram analysis, and PCoA analysis were conducted on populations of D. magna from different regions. The results show that the D. magna genetic relationship between Liaoning and Shanxi, Hunan and Anhui, and Beijing and Hainan are relatively close, while the genetic structure of D. magna in Guangdong, Jiangsu, and Sichuan is quite different from other sampling sites. An analysis of population genetic structure divided the D. magna samples into two major groups.

CONCLUSIONS

These results indicate that the genetic structure of D. magna differs considerably in different regions. Our research results and the newly developed polymorphic SSR markers for D. magna are of great significance in terms of the genetic breeding of D. magna, identification of wild and artificially domesticated populations and conservation genetics research.

摘要

背景

大型溞(Daphnia magna)属于枝角目,在水生态系统中发挥着重要作用。近年来,随着水污染的加剧,大型溞的野生种群数量迅速减少,而分子标记的不足限制了对该物种的有效研究和保护。

方法和结果

采用 RAD-seq 技术,从人工养殖的大型溞和 12 个野生大型溞群体中开发了 26 个新的微卫星(SSR)标记。结果表明,观测杂合度(Ho)和期望杂合度(He)范围分别为 0.083-0.999 和 0.085-0.862,多态信息含量(PIC)范围为 0.368-0.805。这些结果表明,开发的 SSR 标记高度多态。Nei 的遗传身份(H)范围为 0.0926-0.3462。Shannon 的信息指数(I)范围为 0.1333-0.4799。对来自不同地区的大型溞种群进行遗传距离和 Nei 的遗传身份分析、NJ 树图分析和 PCoA 分析。结果表明,辽宁与山西、湖南与安徽、北京与海南的大型溞遗传关系较为密切,而广东、江苏、四川的大型溞遗传结构与其他采样点有较大差异。种群遗传结构分析将大型溞样本分为两大组。

结论

这些结果表明,不同地区的大型溞遗传结构存在较大差异。本研究结果和新开发的大型溞多态性 SSR 标记,对于大型溞的遗传育种、野生和人工养殖群体的鉴定以及保护遗传学研究具有重要意义。

相似文献

1
Development of SSR markers and genetic diversity analysis based on RAD-seq technology among Chinese populations of Daphnia magna.基于 RAD-seq 技术的中国大型溞种群 SSR 标记开发及遗传多样性分析。
Mol Biol Rep. 2022 Jun;49(6):4389-4397. doi: 10.1007/s11033-022-07274-8. Epub 2022 May 12.
2
Genetic Diversity and Population Structure Analysis of Germplasm and Development of a Core Collection Using Microsatellite Markers.利用微卫星标记进行种质遗传多样性和群体结构分析及核心种质库的构建。
Genes (Basel). 2019 Apr 6;10(4):281. doi: 10.3390/genes10040281.
3
[Exploration of transcriptome SSR markers and its application in genetic diversity assessment of Asarum sieboldii].[细辛转录组SSR标记开发及其在遗传多样性评价中的应用]
Zhongguo Zhong Yao Za Zhi. 2023 Oct;48(20):5519-5530. doi: 10.19540/j.cnki.cjcmm.20230623.101.
4
[Evaluation of genetic diversity and population structure of genus Tripterygium based on SSR markers].基于SSR标记的雷公藤属植物遗传多样性与群体结构评价
Yao Xue Xue Bao. 2017 Jan;52(1):153-61.
5
Identification and characterization of functionally relevant SSR markers in natural Dalbergia odorifera populations.天然降香黄檀种群中功能相关SSR标记的鉴定与特征分析
BMC Plant Biol. 2024 Apr 23;24(1):315. doi: 10.1186/s12870-024-05019-2.
6
Genetic structure of Malus sieversii population from Xinjiang, China, revealed by SSR markers.SSR标记揭示的中国新疆塞威氏苹果种群的遗传结构
J Genet Genomics. 2007 Oct;34(10):947-55. doi: 10.1016/S1673-8527(07)60106-4.
7
Genetic diversity of wild soybean populations in Dongying, China, by simple sequence repeat analysis.利用简单序列重复分析对中国东营野生大豆种群的遗传多样性研究
Genet Mol Res. 2015 Sep 28;14(3):11613-23. doi: 10.4238/2015.September.28.13.
8
Genetic diversity and population structure of Polygonatum cyrtonema Hua in China using SSR markers.利用 SSR 标记研究中国玉竹(Polygonatum cyrtonema Hua)的遗传多样性和种群结构。
PLoS One. 2023 Aug 31;18(8):e0290605. doi: 10.1371/journal.pone.0290605. eCollection 2023.
9
Genetic diversity and population structure of the major peanut (Arachis hypogaea L.) cultivars grown in China by SSR markers.利用SSR标记分析中国主要花生(Arachis hypogaea L.)品种的遗传多样性和群体结构
PLoS One. 2014 Feb 10;9(2):e88091. doi: 10.1371/journal.pone.0088091. eCollection 2014.
10
Development of EST-SSR markers and their application in an analysis of the genetic diversity of the endangered species Magnolia sinostellata.EST-SSR 标记的开发及其在濒危物种宝华玉兰遗传多样性分析中的应用。
Mol Genet Genomics. 2019 Feb;294(1):135-147. doi: 10.1007/s00438-018-1493-7. Epub 2018 Sep 25.

引用本文的文献

1
Population Genetic Analysis of from Taro in Japan Using SSR Markers.利用SSR标记对日本芋头进行的群体遗传分析。
J Fungi (Basel). 2023 Mar 23;9(4):391. doi: 10.3390/jof9040391.