Suppr超能文献

如何对基因效应进行有意义的估计。

How to perform meaningful estimates of genetic effects.

作者信息

Alvarez-Castro José M, Le Rouzic Arnaud, Carlborg Orjan

机构信息

Linnaeus Centre for Bioinformatics, Uppsala University, Uppsala, Sweden.

出版信息

PLoS Genet. 2008 May 2;4(5):e1000062. doi: 10.1371/journal.pgen.1000062.

Abstract

Although the genotype-phenotype map plays a central role both in Quantitative and Evolutionary Genetics, the formalization of a completely general and satisfactory model of genetic effects, particularly accounting for epistasis, remains a theoretical challenge. Here, we use a two-locus genetic system in simulated populations with epistasis to show the convenience of using a recently developed model, NOIA, to perform estimates of genetic effects and the decomposition of the genetic variance that are orthogonal even under deviations from the Hardy-Weinberg proportions. We develop the theory for how to use this model in interval mapping of quantitative trait loci using Halley-Knott regressions, and we analyze a real data set to illustrate the advantage of using this approach in practice. In this example, we show that departures from the Hardy-Weinberg proportions that are expected by sampling alone substantially alter the orthogonal estimates of genetic effects when other statistical models, like F2 or G2A, are used instead of NOIA. Finally, for the first time from real data, we provide estimates of functional genetic effects as sets of effects of natural allele substitutions in a particular genotype, which enriches the debate on the interpretation of genetic effects as implemented both in functional and in statistical models. We also discuss further implementations leading to a completely general genotype-phenotype map.

摘要

尽管基因型-表型图谱在数量遗传学和进化遗传学中都起着核心作用,但构建一个完全通用且令人满意的遗传效应模型,尤其是考虑上位性的模型,在理论上仍然是一项挑战。在此,我们在具有上位性的模拟群体中使用双位点遗传系统,以展示使用最近开发的NOIA模型进行遗传效应估计以及遗传方差分解的便利性,即使在偏离哈迪-温伯格比例的情况下,这些估计和分解也是正交的。我们推导了如何使用该模型通过哈利-诺特回归进行数量性状位点区间作图的理论,并分析了一个真实数据集以说明在实际应用中使用这种方法的优势。在这个例子中,我们表明,当使用F2或G2A等其他统计模型而非NOIA时,仅由抽样导致的偏离哈迪-温伯格比例的情况会极大地改变遗传效应的正交估计。最后,我们首次从真实数据中提供了功能遗传效应的估计值,即特定基因型中自然等位基因替换效应的集合,这丰富了在功能模型和统计模型中对遗传效应解释的讨论。我们还讨论了进一步的实现方式,以构建一个完全通用的基因型-表型图谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4b7/2320976/b38bbae9a12f/pgen.1000062.g001.jpg

相似文献

1
How to perform meaningful estimates of genetic effects.
PLoS Genet. 2008 May 2;4(5):e1000062. doi: 10.1371/journal.pgen.1000062.
2
A unified model for functional and statistical epistasis and its application in quantitative trait Loci analysis.
Genetics. 2007 Jun;176(2):1151-67. doi: 10.1534/genetics.106.067348. Epub 2007 Apr 3.
3
Orthogonal Estimates of Variances for Additive, Dominance, and Epistatic Effects in Populations.
Genetics. 2017 Jul;206(3):1297-1307. doi: 10.1534/genetics.116.199406. Epub 2017 May 18.
4
Multiallelic models of genetic effects and variance decomposition in non-equilibrium populations.
Genetica. 2011 Sep;139(9):1119-34. doi: 10.1007/s10709-011-9614-9. Epub 2011 Nov 10.
6
Epistasis of quantitative trait loci under different gene action models.
Genetics. 2004 Jul;167(3):1493-505. doi: 10.1534/genetics.103.020016.
7
Effects of genetic drift on variance components under a general model of epistasis.
Evolution. 2004 Oct;58(10):2111-32. doi: 10.1111/j.0014-3820.2004.tb01591.x.
8
Estimation and interpretation of genetic effects with epistasis using the NOIA model.
Methods Mol Biol. 2012;871:191-204. doi: 10.1007/978-1-61779-785-9_10.
10
Phenotypic evolution from genetic polymorphisms in a radial network architecture.
BMC Biol. 2007 Nov 14;5:50. doi: 10.1186/1741-7007-5-50.

引用本文的文献

2
Analysis of Epistasis in Natural Traits Using Model Organisms.
Trends Genet. 2018 Nov;34(11):883-898. doi: 10.1016/j.tig.2018.08.002. Epub 2018 Aug 27.
3
Two-stage genome-wide search for epistasis with implementation to Recombinant Inbred Lines (RIL) populations.
PLoS One. 2014 Dec 23;9(12):e115680. doi: 10.1371/journal.pone.0115680. eCollection 2014.
4
Detection and replication of epistasis influencing transcription in humans.
Nature. 2014 Apr 10;508(7495):249-53. doi: 10.1038/nature13005. Epub 2014 Feb 26.
5
Natural and orthogonal model for estimating gene-gene interactions applied to cutaneous melanoma.
Hum Genet. 2014 May;133(5):559-74. doi: 10.1007/s00439-013-1392-2. Epub 2013 Nov 17.
6
MAPfastR: quantitative trait loci mapping in outbred line crosses.
G3 (Bethesda). 2013 Dec 9;3(12):2147-9. doi: 10.1534/g3.113.008623.
7
A unified framework integrating parent-of-origin effects for association study.
PLoS One. 2013 Aug 26;8(8):e72208. doi: 10.1371/journal.pone.0072208. eCollection 2013.
8
Current applications of models of genetic effects with interactions across the genome.
Curr Genomics. 2012 Apr;13(2):163-75. doi: 10.2174/138920212799860689.
10
Multiallelic models of genetic effects and variance decomposition in non-equilibrium populations.
Genetica. 2011 Sep;139(9):1119-34. doi: 10.1007/s10709-011-9614-9. Epub 2011 Nov 10.

本文引用的文献

2
A unified model for functional and statistical epistasis and its application in quantitative trait Loci analysis.
Genetics. 2007 Jun;176(2):1151-67. doi: 10.1534/genetics.106.067348. Epub 2007 Apr 3.
5
Detection of SNP epistasis effects of quantitative traits using an extended Kempthorne model.
Physiol Genomics. 2006 Dec 13;28(1):46-52. doi: 10.1152/physiolgenomics.00096.2006. Epub 2006 Aug 29.
6
7
Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations.
Genetics. 2006 Aug;173(4):2269-82. doi: 10.1534/genetics.106.058537. Epub 2006 May 15.
9
Modeling quantitative trait Loci and interpretation of models.
Genetics. 2005 Mar;169(3):1711-25. doi: 10.1534/genetics.104.035857. Epub 2005 Jan 16.
10
Effects of genetic drift on variance components under a general model of epistasis.
Evolution. 2004 Oct;58(10):2111-32. doi: 10.1111/j.0014-3820.2004.tb01591.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验