Mapping epistatic quantitative trait loci

被引:20
作者
Laurie, Cecelia [1 ,2 ]
Wang, Shengchu [3 ]
Carlini-Garcia, Luciana Aparecida [4 ,5 ]
Zeng, Zhao-Bang [3 ,6 ]
机构
[1] Univ Alabama, Dept Math, Tuscaloosa, AL 35487 USA
[2] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[3] N Carolina State Univ, Dept Stat, Bioinformat Res Ctr, Raleigh, NC 27695 USA
[4] Inst Agron Campinas, Ctr Graos & Fibras, Campinas, SP, Brazil
[5] APTA Reg, Polo Ctr Sul, Piracicaba, SP, Brazil
[6] N Carolina State Univ, Dept Biol Sci, Raleigh, NC 27695 USA
关键词
Quantitative trait loci; Epistasis; Model selection; Sequential search; MODEL SELECTION APPROACH; EXPERIMENTAL CROSSES; IDENTIFICATION; ALGORITHM; VARIANCE; QTL;
D O I
10.1186/s12863-014-0112-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: How to map quantitative trait loci (QTL) with epistasis efficiently and reliably has been a persistent problem for QTL mapping analysis. There are a number of difficulties for studying epistatic QTL. Linkage can impose a significant challenge for finding epistatic QTL reliably. If multiple QTL are in linkage and have interactions, searching for QTL can become a very delicate issue. A commonly used strategy that performs a two-dimensional genome scan to search for a pair of QTL with epistasis can suffer from low statistical power and also may lead to false identification due to complex linkage disequilibrium and interaction patterns. Results: To tackle the problem of complex interaction of multiple QTL with linkage, we developed a three-stage search strategy. In the first stage, main effect QTL are searched and mapped. In the second stage, epistatic QTL that interact significantly with other identified QTL are searched. In the third stage, new epistatic QTL are searched in pairs. This strategy is based on the consideration that most genetic variance is due to the main effects of QTL. Thus by first mapping those main-effect QTL, the statistical power for the second and third stages of analysis for mapping epistatic QTL can be maximized. The search for main effect QTL is robust and does not bias the search for epistatic QTL due to a genetic property associated with the orthogonal genetic model that the additive and additive by additive variances are independent despite of linkage. The model search criterion is empirically and dynamically evaluated by using a score-statistic based resampling procedure. We demonstrate through simulations that the method has good power and low false positive in the identification of QTL and epistasis. Conclusion: This method provides an effective and powerful solution to map multiple QTL with complex epistatic pattern. The method has been implemented in the user-friendly computer software Windows QTL Cartographer. This will greatly facilitate the application of the method for QTL mapping data analysis.
引用
收藏
页数:13
相关论文
共 21 条
[1]   A model selection approach for the identification of quantitative trait loci in experimental crosses [J].
Broman, KW ;
Speed, TP .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 2002, 64 :641-656
[2]  
Carlborg Ö, 2000, GENETICS, V155, P2003
[3]   Simultaneous mapping of epistatic QTL in DU6i x DBA/2 mice [J].
Carlborg, Ö ;
Brockmann, GA ;
Haley, CS .
MAMMALIAN GENOME, 2005, 16 (07) :481-494
[4]  
CHURCHILL GA, 1994, GENETICS, V138, P963
[5]  
Doerge RW, 1996, GENETICS, V142, P285
[6]   Mapping quantitative trait loci with dominant and missing markers in various crosses from two inbred lines [J].
Jiang, CJ ;
Zeng, ZB .
GENETICA, 1997, 101 (01) :47-58
[7]   General formulas for obtaining the MLEs and the asymptotic variance-covariance matrix in mapping quantitative trait loci when using the EM algorithm [J].
Kao, CH ;
Zeng, ZB .
BIOMETRICS, 1997, 53 (02) :653-665
[8]  
Kao CH, 1999, GENETICS, V152, P1203
[9]   Poor performance of bootstrap confidence intervals for the location of a quantitative trait locus [J].
Manichaikul, Ani ;
Dupuis, Josee ;
Sen, Saunak ;
Broman, Karl W. .
GENETICS, 2006, 174 (01) :481-489
[10]   A Model Selection Approach for the Identification of Quantitative Trait Loci in Experimental Crosses, Allowing Epistasis [J].
Manichaikul, Ani ;
Moon, Jee Young ;
Sen, Saunak ;
Yandell, Brian S. ;
Broman, Karl W. .
GENETICS, 2009, 181 (03) :1077-1086