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A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation

How one trait developmentally varies as a function of others shapes a spectrum of biological phenomena. Despite its importance to trait dissection, the understanding of whether and how genes mediate such developmental covariation is poorly understood. We integrate developmental allometry equations i...

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Autores principales: Jiang, Libo, Shi, Hexin, Sang, Mengmeng, Zheng, Chenfei, Cao, Yige, Zhu, Xuli, Zhuo, Xiaokang, Cheng, Tangren, Zhang, Qixiang, Wu, Rongling, Sun, Lidan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930182/
https://www.ncbi.nlm.nih.gov/pubmed/31921232
http://dx.doi.org/10.3389/fpls.2019.01557
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author Jiang, Libo
Shi, Hexin
Sang, Mengmeng
Zheng, Chenfei
Cao, Yige
Zhu, Xuli
Zhuo, Xiaokang
Cheng, Tangren
Zhang, Qixiang
Wu, Rongling
Sun, Lidan
author_facet Jiang, Libo
Shi, Hexin
Sang, Mengmeng
Zheng, Chenfei
Cao, Yige
Zhu, Xuli
Zhuo, Xiaokang
Cheng, Tangren
Zhang, Qixiang
Wu, Rongling
Sun, Lidan
author_sort Jiang, Libo
collection PubMed
description How one trait developmentally varies as a function of others shapes a spectrum of biological phenomena. Despite its importance to trait dissection, the understanding of whether and how genes mediate such developmental covariation is poorly understood. We integrate developmental allometry equations into the functional mapping framework to map specific QTLs that govern the correlated development of different traits. Based on evolutionary game theory, we assemble and contextualize these QTLs into an intricate but organized network coded by bidirectional, signed, and weighted QTL-QTL interactions. We use this approach to map shoot height-diameter allometry QTLs in an ornamental woody species, mei (Prunus mume). We detect “pioneering” QTLs (piQTLs) and “maintaining” QTLs (miQTLs) that determine how shoot height varies with diameter and how shoot diameter varies with height, respectively. The QTL networks inferred can visualize how each piQTL regulates others to promote height growth at a cost of diameter growth, how miQTL regulates others to benefit radial growth at a cost of height growth, and how piQTLs and miQTLs regulate each other to form a pleiotropic web of primary and secondary growth in trees. Our approach provides a unique gateway to explore the genetic architecture of developmental covariation, a widespread phenomenon in nature.
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spelling pubmed-69301822020-01-09 A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation Jiang, Libo Shi, Hexin Sang, Mengmeng Zheng, Chenfei Cao, Yige Zhu, Xuli Zhuo, Xiaokang Cheng, Tangren Zhang, Qixiang Wu, Rongling Sun, Lidan Front Plant Sci Plant Science How one trait developmentally varies as a function of others shapes a spectrum of biological phenomena. Despite its importance to trait dissection, the understanding of whether and how genes mediate such developmental covariation is poorly understood. We integrate developmental allometry equations into the functional mapping framework to map specific QTLs that govern the correlated development of different traits. Based on evolutionary game theory, we assemble and contextualize these QTLs into an intricate but organized network coded by bidirectional, signed, and weighted QTL-QTL interactions. We use this approach to map shoot height-diameter allometry QTLs in an ornamental woody species, mei (Prunus mume). We detect “pioneering” QTLs (piQTLs) and “maintaining” QTLs (miQTLs) that determine how shoot height varies with diameter and how shoot diameter varies with height, respectively. The QTL networks inferred can visualize how each piQTL regulates others to promote height growth at a cost of diameter growth, how miQTL regulates others to benefit radial growth at a cost of height growth, and how piQTLs and miQTLs regulate each other to form a pleiotropic web of primary and secondary growth in trees. Our approach provides a unique gateway to explore the genetic architecture of developmental covariation, a widespread phenomenon in nature. Frontiers Media S.A. 2019-12-18 /pmc/articles/PMC6930182/ /pubmed/31921232 http://dx.doi.org/10.3389/fpls.2019.01557 Text en Copyright © 2019 Jiang, Shi, Sang, Zheng, Cao, Zhu, Zhuo, Cheng, Zhang, Wu and Sun http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Jiang, Libo
Shi, Hexin
Sang, Mengmeng
Zheng, Chenfei
Cao, Yige
Zhu, Xuli
Zhuo, Xiaokang
Cheng, Tangren
Zhang, Qixiang
Wu, Rongling
Sun, Lidan
A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation
title A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation
title_full A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation
title_fullStr A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation
title_full_unstemmed A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation
title_short A Computational Model for Inferring QTL Control Networks Underlying Developmental Covariation
title_sort computational model for inferring qtl control networks underlying developmental covariation
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930182/
https://www.ncbi.nlm.nih.gov/pubmed/31921232
http://dx.doi.org/10.3389/fpls.2019.01557
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