scholarly journals Genetic architecture of growth traits in Populus revealed by integrated quantitative trait locus ( QTL ) analysis and association studies

2015 ◽  
Vol 209 (3) ◽  
pp. 1067-1082 ◽  
Author(s):  
Qingzhang Du ◽  
Chenrui Gong ◽  
Qingshi Wang ◽  
Daling Zhou ◽  
Haijiao Yang ◽  
...  
2018 ◽  
Vol 294 (1) ◽  
pp. 243-252 ◽  
Author(s):  
Tatsuhiko Goto ◽  
Akira Ishikawa ◽  
Masahide Nishibori ◽  
Masaoki Tsudzuki

2009 ◽  
Vol 6 (2) ◽  
pp. 305-317 ◽  
Author(s):  
Bala R. Thumma ◽  
Simon G. Southerton ◽  
John C. Bell ◽  
John V. Owen ◽  
Martin L. Henery ◽  
...  

2012 ◽  
Vol 12 (1) ◽  
pp. 30 ◽  
Author(s):  
Yung-Fen Huang ◽  
Agnès Doligez ◽  
Alexandre Fournier-Level ◽  
Loïc Le Cunff ◽  
Yves Bertrand ◽  
...  

2010 ◽  
Vol 6 (6) ◽  
pp. 877-889 ◽  
Author(s):  
Bala R. Thumma ◽  
Brian S. Baltunis ◽  
John C. Bell ◽  
Livinus C. Emebiri ◽  
Gavin F. Moran ◽  
...  

2021 ◽  
Author(s):  
Alex N. Nguyen Ba ◽  
Katherine R. Lawrence ◽  
Artur Rego-Costa ◽  
Shreyas Gopalakrishnan ◽  
Daniel Temko ◽  
...  

Mapping the genetic basis of complex traits is critical to uncovering the biological mechanisms that underlie disease and other phenotypes. Genome-wide association studies (GWAS) in humans and quantitative trait locus (QTL) mapping in model organisms can now explain much of the observed heritability in many traits, allowing us to predict phenotype from genotype. However, constraints on power due to statistical confounders in large GWAS and smaller sample sizes in QTL studies still limit our ability to resolve numerous small-effect variants, map them to causal genes, identify pleiotropic effects across multiple traits, and infer non-additive interactions between loci (epistasis). Here, we introduce barcoded bulk quantitative trait locus (BB-QTL) mapping, which allows us to construct, genotype, and phenotype 100,000 offspring of a budding yeast cross, two orders of magnitude larger than the previous state of the art. We use this panel to map the genetic basis of eighteen complex traits, finding that the genetic architecture of these traits involves hundreds of small-effect loci densely spaced throughout the genome, many with widespread pleiotropic effects across multiple traits. Epistasis plays a central role, with thousands of interactions that provide insight into genetic networks. By dramatically increasing sample size, BB-QTL mapping demonstrates the potential of natural variants in high-powered QTL studies to reveal the highly polygenic, pleiotropic, and epistatic architecture of complex traits.Significance statementUnderstanding the genetic basis of important phenotypes is a central goal of genetics. However, the highly polygenic architectures of complex traits inferred by large-scale genome-wide association studies (GWAS) in humans stand in contrast to the results of quantitative trait locus (QTL) mapping studies in model organisms. Here, we use a barcoding approach to conduct QTL mapping in budding yeast at a scale two orders of magnitude larger than the previous state of the art. The resulting increase in power reveals the polygenic nature of complex traits in yeast, and offers insight into widespread patterns of pleiotropy and epistasis. Our data and analysis methods offer opportunities for future work in systems biology, and have implications for large-scale GWAS in human populations.


Author(s):  
Hannah E. Bainbridge ◽  
Melanie N. Brien ◽  
Carlos Morochz ◽  
Patricio A. Salazar ◽  
Pasi Rastas ◽  
...  

AbstractMimetic systems allow us to address the question of whether the same genes control similar phenotypes in different species. Although widespread parallels have been found for major effect loci, much less is known about genes that control quantitative trait variation. In this study, we identify and compare the loci that control subtle changes in the size and shape of forewing pattern elements in two Heliconius butterfly co-mimics. We use quantitative trait locus (QTL) analysis with a multivariate phenotyping approach to map the variation in red pattern elements across the whole forewing surface of Heliconius erato and Heliconius melpomene. These results are compared to a QTL analysis of univariate trait changes, and show that our resolution for identifying small effect loci is improved with the multivariate approach. QTL likely corresponding to the known patterning gene optix were found in both species but otherwise, a remarkably low level of genetic parallelism was found. This lack of similarity indicates that the genetic basis of convergent traits may not be as predictable as assumed from studies that focus solely on Mendelian traits.


2019 ◽  
Vol 144 (5) ◽  
pp. 352-362
Author(s):  
Vanessa E.T.M. Ashworth ◽  
Haofeng Chen ◽  
Carlos L. Calderón-Vázquez ◽  
Mary Lu Arpaia ◽  
David N. Kuhn ◽  
...  

The glossy, green-fleshed fruit of the avocado (Persea americana) has been the object of human selection for thousands of years. Recent interest in healthy nutrition has singled out the avocado as an excellent source of several phytonutrients. Yet as a sizeable, slow-maturing tree crop, it has been largely neglected by genetic studies, owing to a long breeding cycle and costly field trials. We use a small, replicated experimental population of 50 progeny, grown at two locations in two successive years, to explore the feasibility of developing a dense genetic linkage map and to implement quantitative trait locus (QTL) analysis for seven phenotypic traits. Additionally, we test the utility of candidate-gene single-nucleotide polymorphisms developed to genes from biosynthetic pathways of phytonutrients beneficial to human health. The resulting linkage map consisted of 1346 markers (1044.7 cM) distributed across 12 linkage groups. Numerous markers on Linkage Group 10 were associated with a QTL for flowering type. One marker on Linkage Group 1 tracked a QTL for β-sitosterol content of the fruit. A region on Linkage Group 3 tracked vitamin E (α-tocopherol) content of the fruit, and several markers were stable across both locations and study years. We argue that the pursuit of linkage mapping and QTL analysis is worthwhile, even when population size is small.


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