• 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

支持维持健康传统暹罗猫种群的统计分析。

Statistical analysis in support of maintaining a healthy traditional Siamese cat population.

作者信息

Pistorius Arthur M A, Blokker Ineke

机构信息

260 Centre for Molecular and Biomolecular Informatics, Radboud University Medical Centre, PO Box 9101, NL-6500 HB, Nijmegen, The Netherlands.

Workgroup Traditional Siamese Cat Breeders in The Netherlands (WTSN), NL-1815 HC, Alkmaar, The Netherlands.

出版信息

Genet Sel Evol. 2021 Jan 6;53(1):6. doi: 10.1186/s12711-020-00596-w.

DOI:10.1186/s12711-020-00596-w
PMID:33407084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7789816/
Abstract

BACKGROUND

For many years, breeders of companion animals have applied inbreeding or line breeding to transfer desirable genetic traits from parents to their offspring. Simultaneously, this resulted in a considerable spread of hereditary diseases and phenomena associated with inbreeding depression.

RESULTS

Our cluster analysis of kinship and inbreeding coefficients suggests that the Thai or traditional Siamese cat could be considered as a subpopulation of the Siamese cat, which shares common ancestors, although they are considered as separate breeds. In addition, model-based cluster analysis could detect regional differences between Thai subpopulations. We show that by applying optimal contribution selection and simultaneously limiting the contributions by other breeds, the genetic diversity within subpopulations can be improved.

CONCLUSION

In principle, the European mainland Thai cat population can achieve a genetic diversity of about 26 founder genome equivalents, a value that could potentially sustain a genetically diverse population. However, reaching such a target will be difficult in the absence of a supervised breeding program. Suboptimal solutions can be obtained by minimisation of kinships within regional subpopulations. Exchanging animals between different regions on a small scale might be already quite useful to reduce the kinship, by achieving a potential diversity of 23 founder genome equivalents. However, contributions by other breeds should be minimised to preserve the original Siamese gene pool.

摘要

背景

多年来,伴侣动物饲养者一直采用近亲繁殖或品系繁育,将理想的遗传性状从亲代传递给子代。与此同时,这导致了遗传疾病以及与近亲繁殖衰退相关现象的大量传播。

结果

我们对亲缘系数和近亲繁殖系数的聚类分析表明,泰国猫或传统暹罗猫可被视为暹罗猫的一个亚群体,它们拥有共同的祖先,尽管它们被视为不同的品种。此外,基于模型的聚类分析能够检测泰国亚群体之间的区域差异。我们表明,通过应用最优贡献选择并同时限制其他品种的贡献,可以提高亚群体内部的遗传多样性。

结论

原则上,欧洲大陆的泰国猫种群能够实现约26个奠基者基因组当量的遗传多样性,这一数值有可能维持一个基因多样化的种群。然而,在缺乏监督繁育计划的情况下,实现这一目标将很困难。通过最小化区域亚群体内部的亲缘关系可以获得次优解决方案。在不同区域之间小规模交换动物可能已经十分有助于降低亲缘关系,从而实现23个奠基者基因组当量的潜在多样性。然而,应尽量减少其他品种的贡献,以保护原始的暹罗猫基因库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/8df655a76fad/12711_2020_596_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/df978a1e23db/12711_2020_596_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/6d0e15e91b0b/12711_2020_596_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/95d5c03640fe/12711_2020_596_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/8333afa86b08/12711_2020_596_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/43df65625399/12711_2020_596_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/873beb2c3a2f/12711_2020_596_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/673126e19fde/12711_2020_596_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/8df655a76fad/12711_2020_596_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/df978a1e23db/12711_2020_596_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/6d0e15e91b0b/12711_2020_596_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/95d5c03640fe/12711_2020_596_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/8333afa86b08/12711_2020_596_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/43df65625399/12711_2020_596_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/873beb2c3a2f/12711_2020_596_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/673126e19fde/12711_2020_596_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7789816/8df655a76fad/12711_2020_596_Fig8_HTML.jpg

相似文献

1
Statistical analysis in support of maintaining a healthy traditional Siamese cat population.支持维持健康传统暹罗猫种群的统计分析。
Genet Sel Evol. 2021 Jan 6;53(1):6. doi: 10.1186/s12711-020-00596-w.
2
Novel optimum contribution selection methods accounting for conflicting objectives in breeding programs for livestock breeds with historical migration.考虑历史迁移的家畜品种育种计划中冲突目标的新型最优贡献选择方法。
Genet Sel Evol. 2017 May 12;49(1):45. doi: 10.1186/s12711-017-0320-7.
3
Mucopolysaccharidosis VI in cats - clarification regarding genetic testing.猫的黏多糖贮积症VI型——关于基因检测的说明
BMC Vet Res. 2016 Jul 2;12(1):136. doi: 10.1186/s12917-016-0764-y.
4
Genetic relationships and inbreeding levels among geographically distant populations of Felis catus from Japan and the United States.日本和美国地理上相距甚远的家猫种群的遗传关系和近亲繁殖水平。
Genomics. 2021 Jan;113(1 Pt 1):104-110. doi: 10.1016/j.ygeno.2020.11.018. Epub 2020 Nov 25.
5
Shared alleles and genetic structures in different Thai domestic cat breeds: the possible influence of common racial origins.不同泰国家猫品种的共享等位基因和遗传结构:共同种族起源的可能影响。
Genomics Inform. 2024 Jul 31;22(1):12. doi: 10.1186/s44342-024-00013-4.
6
Advanced optimum contribution selection as a tool to improve regional cattle breeds: a feasibility study for Vorderwald cattle.高级最优贡献选择作为提高地区牛种的工具:Vorderwald 牛的可行性研究。
Animal. 2020 Jan;14(1):1-12. doi: 10.1017/S1751731119001484. Epub 2019 Jul 12.
7
Pedigree analysis of Abyssinian cats with familial amyloidosis.患有家族性淀粉样变性的阿比西尼亚猫的系谱分析。
Am J Vet Res. 1986 Dec;47(12):2666-8.
8
Trends in genome-wide and region-specific genetic diversity in the Dutch-Flemish Holstein-Friesian breeding program from 1986 to 2015.1986 年至 2015 年荷兰-佛兰芒荷斯坦-弗里森牛种畜群的全基因组和特定区域遗传多样性趋势。
Genet Sel Evol. 2018 Apr 11;50(1):15. doi: 10.1186/s12711-018-0385-y.
9
Estimates of genetic diversity in the brown cattle population of Switzerland obtained from pedigree information.根据系谱信息得出的瑞士褐牛种群遗传多样性估计值。
J Anim Breed Genet. 2005 Dec;122(6):405-13. doi: 10.1111/j.1439-0388.2005.00552.x.
10
Inbreeding rate and genetic structure of cat populations in Poland.波兰猫种群的近交率和遗传结构。
J Appl Genet. 2011 Feb;52(1):101-10. doi: 10.1007/s13353-010-0018-9. Epub 2010 Dec 3.

引用本文的文献

1
Shared alleles and genetic structures in different Thai domestic cat breeds: the possible influence of common racial origins.不同泰国家猫品种的共享等位基因和遗传结构:共同种族起源的可能影响。
Genomics Inform. 2024 Jul 31;22(1):12. doi: 10.1186/s44342-024-00013-4.
2
Tracking footprints of artificial and natural selection signatures in breeding and non-breeding cats.追踪人工选择和自然选择特征在繁殖期和非繁殖期猫科动物中的印记。
Sci Rep. 2022 Oct 27;12(1):18061. doi: 10.1038/s41598-022-22155-7.
3
Feline Fertility: Consequences of inbreeding and implications for reproductive fitness.

本文引用的文献

1
Optimum contribution selection for animal breeding and conservation: the R package optiSel.动物选育和保护的最优贡献选择:optisel R 包。
BMC Bioinformatics. 2019 Jan 14;20(1):25. doi: 10.1186/s12859-018-2450-5.
2
An insight into population structure and gene flow within pure-bred cats.对纯种猫种群结构和基因流动的洞察。
J Anim Breed Genet. 2014 Feb;131(1):53-60. doi: 10.1111/jbg.12043. Epub 2013 Jun 6.
3
Optimum contribution selection for conserved populations with historic migration.具有历史迁移的保守群体的最优贡献选择。
猫科动物的繁殖力:近亲繁殖的后果及其对生殖适应性的影响。
J Feline Med Surg. 2022 Sep;24(9):847-852. doi: 10.1177/1098612X221118755.
4
Reproductive Management in Catteries: Optimising health and wellbeing through veterinarian-breeder collaboration.猫舍的繁殖管理:通过兽医-繁育者合作优化健康和福利。
J Feline Med Surg. 2022 Sep;24(9):881-904. doi: 10.1177/1098612X221118760.
Genet Sel Evol. 2012 Nov 15;44(1):34. doi: 10.1186/1297-9686-44-34.
4
A population genetic database of cat breeds developed in coordination with a domestic cat STR multiplex.一个与家猫STR复合扩增体系协作开发的猫品种群体遗传数据库。
J Forensic Sci. 2012 May;57(3):596-601. doi: 10.1111/j.1556-4029.2011.02040.x. Epub 2012 Jan 23.
5
Inbreeding rate and genetic structure of cat populations in Poland.波兰猫种群的近交率和遗传结构。
J Appl Genet. 2011 Feb;52(1):101-10. doi: 10.1007/s13353-010-0018-9. Epub 2010 Dec 3.
6
Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds.在大量受欢迎的猫品种中发现了广泛的视网膜退行性疾病突变(rdAc)。
Vet J. 2010 Oct;186(1):32-8. doi: 10.1016/j.tvjl.2009.08.010. Epub 2009 Sep 10.
7
History and structure of the closed pedigreed population of Icelandic Sheepdogs.冰岛牧羊犬封闭谱系群体的历史与结构。
Genet Sel Evol. 2009 Aug 6;41(1):39. doi: 10.1186/1297-9686-41-39.
8
The ascent of cat breeds: genetic evaluations of breeds and worldwide random-bred populations.猫品种的崛起:品种及全球随机繁殖群体的遗传评估
Genomics. 2008 Jan;91(1):12-21. doi: 10.1016/j.ygeno.2007.10.009. Epub 2007 Dec 3.
9
Assessing the contribution of breeds to genetic diversity in conservation schemes.评估品种对保护计划中遗传多样性的贡献。
Genet Sel Evol. 2002 Sep-Oct;34(5):613-33. doi: 10.1186/1297-9686-34-5-613.
10
Cluster analysis of the genetic heterogeneity and disease distributions in purebred dog populations.
Vet Rec. 1998 Feb 28;142(9):209-13. doi: 10.1136/vr.142.9.209.