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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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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. |
format | Online Article Text |
id | pubmed-6930182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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