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黄斑龙虾(Panulirus guttatus)八个多态微卫星的分离与特征分析。

Isolation and characterization of eight polymorphic microsatellites for the spotted spiny lobster, Panulirus guttatus.

作者信息

Truelove Nathan, Behringer Donald C, Butler Iv Mark J, Preziosi Richard F

机构信息

Faculty of Life Sciences, University of Manchester, Manchester, England; Current affiliation: Smithsonian Museum of Natural History, Smithsonian Marine Station, Fort Pierce, FL, United States.

School of Forest Resources and Conservation & Emerging Pathogens Institute, University of Florida , Gainesville, FL , United States.

出版信息

PeerJ. 2016 Jan 25;4:e1467. doi: 10.7717/peerj.1467. eCollection 2016.

Abstract

Microsatellite sequences were isolated from enriched genomic libraries of the spotted spiny lobster, Panulirus guttatus using 454 pyrosequencing. Twenty-nine previously developed polymerase chain reaction primer pairs of Panulirus argus microsatellite loci were also tested for cross-species amplification in Panulirus guttatus. In total, eight consistently amplifying, and polymorphic loci were characterized for 57 individuals collected in the Florida Keys and Bermuda. The number of alleles per locus ranged from 8 to 20 and observed heterozygosities ranged from 0.409 to 0.958. Significant deviations from Hardy-Weinberg equilibrium were found in one locus from Florida and three loci from Bermuda. Quality control testing indicated that all loci were easy to score, highly polymorphic and showed no evidence of linkage disequilibrium. Null alleles were detected in three loci with moderate frequencies ranging from (20% to 22%). These eight microsatellites provide novel molecular markers for future conservation genetics research of P. guttatus.

摘要

利用454焦磷酸测序技术,从多斑刺龙虾(Panulirus guttatus)的富集基因组文库中分离出微卫星序列。还测试了29对先前开发的锦绣龙虾(Panulirus argus)微卫星位点的聚合酶链反应引物对,以用于多斑刺龙虾的跨物种扩增。总共对在佛罗里达群岛和百慕大收集的57个个体的8个一致性扩增且具有多态性的位点进行了表征。每个位点的等位基因数从8到20不等,观察到的杂合度从0.409到0.958不等。在来自佛罗里达的一个位点和来自百慕大的三个位点中发现了显著偏离哈迪-温伯格平衡的情况。质量控制测试表明,所有位点易于评分,高度多态,且未显示连锁不平衡的证据。在三个位点中检测到无效等位基因,其频率适中,范围为(20%至22%)。这八个微卫星为未来多斑刺龙虾的保护遗传学研究提供了新的分子标记。

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