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开发一个包含499个食蟹猴新型微卫星标记的综合数据库。

Development of an integrative database with 499 novel microsatellite markers for Macaca fascicularis.

作者信息

Higashino Atsunori, Osada Naoki, Suto Yumiko, Hirata Makoto, Kameoka Yosuke, Takahashi Ichiro, Terao Keiji

机构信息

Tsukuba Primate Research Center, National Institute of Biomedical Innovation, Tsukuba, Ibaraki, Japan.

出版信息

BMC Genet. 2009 Jun 5;10:24. doi: 10.1186/1471-2156-10-24.

Abstract

BACKGROUND

Cynomolgus macaques (Macaca fascicularis) are a valuable resource for linkage studies of genetic disorders, but their microsatellite markers are not sufficient. In genetic studies, a prerequisite for mapping genes is development of a genome-wide set of microsatellite markers in target organisms. A whole genome sequence and its annotation also facilitate identification of markers for causative mutations. The aim of this study is to establish hundreds of microsatellite markers and to develop an integrative cynomolgus macaque genome database with a variety of datasets including marker and gene information that will be useful for further genetic analyses in this species.

RESULTS

We investigated the level of polymorphisms in cynomolgus monkeys for 671 microsatellite markers that are covered by our established Bacterial Artificial Chromosome (BAC) clones. Four hundred and ninety-nine (74.4%) of the markers were found to be polymorphic using standard PCR analysis. The average number of alleles and average expected heterozygosity at these polymorphic loci in ten cynomolgus macaques were 8.20 and 0.75, respectively.

CONCLUSION

BAC clones and novel microsatellite markers were assigned to the rhesus genome sequence and linked with our cynomolgus macaque cDNA database (QFbase). Our novel microsatellite marker set and genomic database will be valuable integrative resources in analyzing genetic disorders in cynomolgus macaques.

摘要

背景

食蟹猴(猕猴属)是遗传疾病连锁研究的宝贵资源,但它们的微卫星标记并不充足。在遗传学研究中,绘制基因图谱的一个先决条件是在目标生物体中开发一套全基因组微卫星标记。全基因组序列及其注释也有助于识别致病突变的标记。本研究的目的是建立数百个微卫星标记,并开发一个整合的食蟹猴基因组数据库,其中包含各种数据集,包括标记和基因信息,这将有助于对该物种进行进一步的遗传分析。

结果

我们研究了食蟹猴中671个微卫星标记的多态性水平,这些标记由我们建立的细菌人工染色体(BAC)克隆覆盖。使用标准PCR分析发现,499个(74.4%)标记具有多态性。在十只食蟹猴中,这些多态位点的平均等位基因数和平均预期杂合度分别为8.20和0.75。

结论

BAC克隆和新型微卫星标记被分配到恒河猴基因组序列,并与我们的食蟹猴cDNA数据库(QFbase)相关联。我们的新型微卫星标记集和基因组数据库将成为分析食蟹猴遗传疾病的宝贵整合资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2eb/2702342/7e51368c99b8/1471-2156-10-24-1.jpg

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