Dissecting genetic networks underlying complex phenotypes: The theoretical framework

Great progress has been made in genetic dissection of quantitative trait variation during the past two decades, but many studies still reveal only a small fraction of quantitative trait loci (QTLs), and epistasis remains elusive. We integrate contemporary knowledge of signal transduction pathways wi...

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Autores principales: Zhang, Fan, Zhai, Hu-Qu, Paterson, Andrew H., Xu, Jianlong, Gao, Yong-Ming, Zheng, Tianqing, Wu, Rong-Ling, Fu, Binying, Ali, Jauhar, Li, Zhikang
Formato: Journal Article
Lenguaje:Inglés
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://hdl.handle.net/10568/165942
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author Zhang, Fan
Zhai, Hu-Qu
Paterson, Andrew H.
Xu, Jianlong
Gao, Yong-Ming
Zheng, Tianqing
Wu, Rong-Ling
Fu, Binying
Ali, Jauhar
Li, Zhikang
author_browse Ali, Jauhar
Fu, Binying
Gao, Yong-Ming
Li, Zhikang
Paterson, Andrew H.
Wu, Rong-Ling
Xu, Jianlong
Zhai, Hu-Qu
Zhang, Fan
Zheng, Tianqing
author_facet Zhang, Fan
Zhai, Hu-Qu
Paterson, Andrew H.
Xu, Jianlong
Gao, Yong-Ming
Zheng, Tianqing
Wu, Rong-Ling
Fu, Binying
Ali, Jauhar
Li, Zhikang
author_sort Zhang, Fan
collection Repository of Agricultural Research Outputs (CGSpace)
description Great progress has been made in genetic dissection of quantitative trait variation during the past two decades, but many studies still reveal only a small fraction of quantitative trait loci (QTLs), and epistasis remains elusive. We integrate contemporary knowledge of signal transduction pathways with principles of quantitative and population genetics to characterize genetic networks underlying complex traits, using a model founded upon one-way functional dependency of downstream genes on upstream regulators (the principle of hierarchy) and mutual functional dependency among related genes (functional genetic units, FGU). Both simulated and real data suggest that complementary epistasis contributes greatly to quantitative trait variation, and obscures the phenotypic effects of many ‘downstream’ loci in pathways. The mathematical relationships between the main effects and epistatic effects of genes acting at different levels of signaling pathways were established using the quantitative and population genetic parameters. Both loss of function and “co-adapted” gene complexes formed by multiple alleles with differentiated functions (effects) are predicted to be frequent types of allelic diversity at loci that contribute to the genetic variation of complex traits in populations. Downstream FGUs appear to be more vulnerable to loss of function than their upstream regulators, but this vulnerability is apparently compensated by different FGUs of similar functions. Other predictions from the model may account for puzzling results regarding responses to selection, genotype by environment interaction, and the genetic basis of heterosis.
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spelling CGSpace1659422025-05-14T10:24:26Z Dissecting genetic networks underlying complex phenotypes: The theoretical framework Zhang, Fan Zhai, Hu-Qu Paterson, Andrew H. Xu, Jianlong Gao, Yong-Ming Zheng, Tianqing Wu, Rong-Ling Fu, Binying Ali, Jauhar Li, Zhikang alleles gene interaction genetic variation genetics genotypes heterosis phenotypes quantitative trait loci quantitative traits signal transduction Great progress has been made in genetic dissection of quantitative trait variation during the past two decades, but many studies still reveal only a small fraction of quantitative trait loci (QTLs), and epistasis remains elusive. We integrate contemporary knowledge of signal transduction pathways with principles of quantitative and population genetics to characterize genetic networks underlying complex traits, using a model founded upon one-way functional dependency of downstream genes on upstream regulators (the principle of hierarchy) and mutual functional dependency among related genes (functional genetic units, FGU). Both simulated and real data suggest that complementary epistasis contributes greatly to quantitative trait variation, and obscures the phenotypic effects of many ‘downstream’ loci in pathways. The mathematical relationships between the main effects and epistatic effects of genes acting at different levels of signaling pathways were established using the quantitative and population genetic parameters. Both loss of function and “co-adapted” gene complexes formed by multiple alleles with differentiated functions (effects) are predicted to be frequent types of allelic diversity at loci that contribute to the genetic variation of complex traits in populations. Downstream FGUs appear to be more vulnerable to loss of function than their upstream regulators, but this vulnerability is apparently compensated by different FGUs of similar functions. Other predictions from the model may account for puzzling results regarding responses to selection, genotype by environment interaction, and the genetic basis of heterosis. 2011-01-20 2024-12-19T12:55:39Z 2024-12-19T12:55:39Z Journal Article https://hdl.handle.net/10568/165942 en Open Access Public Library of Science Zhang, Fan; Zhai, Hu-Qu; Paterson, Andrew H.; Xu, Jian-Long; Gao, Yong-Ming; Zheng, Tian-Qing; Wu, Rong-Ling; Fu, Bin-Ying; Ali, Jauhar and Li, Zhi-Kang. 2011. Dissecting genetic networks underlying complex phenotypes: The theoretical framework. PLoS ONE, Volume 6 no. 1 p. e14541
spellingShingle alleles
gene interaction
genetic variation
genetics
genotypes
heterosis
phenotypes
quantitative trait loci
quantitative traits
signal transduction
Zhang, Fan
Zhai, Hu-Qu
Paterson, Andrew H.
Xu, Jianlong
Gao, Yong-Ming
Zheng, Tianqing
Wu, Rong-Ling
Fu, Binying
Ali, Jauhar
Li, Zhikang
Dissecting genetic networks underlying complex phenotypes: The theoretical framework
title Dissecting genetic networks underlying complex phenotypes: The theoretical framework
title_full Dissecting genetic networks underlying complex phenotypes: The theoretical framework
title_fullStr Dissecting genetic networks underlying complex phenotypes: The theoretical framework
title_full_unstemmed Dissecting genetic networks underlying complex phenotypes: The theoretical framework
title_short Dissecting genetic networks underlying complex phenotypes: The theoretical framework
title_sort dissecting genetic networks underlying complex phenotypes the theoretical framework
topic alleles
gene interaction
genetic variation
genetics
genotypes
heterosis
phenotypes
quantitative trait loci
quantitative traits
signal transduction
url https://hdl.handle.net/10568/165942
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