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iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover

Integrating omics data with quantification of biological traits provides unparalleled opportunities for discovery of genetic regulators by in silico inference. However, current approaches to analyze genetic-perturbation screens are limited by their reliance on annotation libraries for prioritization...

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Autores principales: Huang, Jia-Hsin, Liao, You-Rou, Lin, Tzu-Chieh, Tsai, Cheng-Hung, Lai, Wei-Yun, Chou, Yang-Kai, Leu, Jun-Yi, Tsai, Huai-Kuang, Kao, Cheng-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287957/
https://www.ncbi.nlm.nih.gov/pubmed/34197604
http://dx.doi.org/10.1093/nar/gkab555
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author Huang, Jia-Hsin
Liao, You-Rou
Lin, Tzu-Chieh
Tsai, Cheng-Hung
Lai, Wei-Yun
Chou, Yang-Kai
Leu, Jun-Yi
Tsai, Huai-Kuang
Kao, Cheng-Fu
author_facet Huang, Jia-Hsin
Liao, You-Rou
Lin, Tzu-Chieh
Tsai, Cheng-Hung
Lai, Wei-Yun
Chou, Yang-Kai
Leu, Jun-Yi
Tsai, Huai-Kuang
Kao, Cheng-Fu
author_sort Huang, Jia-Hsin
collection PubMed
description Integrating omics data with quantification of biological traits provides unparalleled opportunities for discovery of genetic regulators by in silico inference. However, current approaches to analyze genetic-perturbation screens are limited by their reliance on annotation libraries for prioritization of hits and subsequent targeted experimentation. Here, we present iTARGEX (identification of Trait-Associated Regulatory Genes via mixture regression using EXpectation maximization), an association framework with no requirement of a priori knowledge of gene function. After creating this tool, we used it to test associations between gene expression profiles and two biological traits in single-gene deletion budding yeast mutants, including transcription homeostasis during S phase and global protein turnover. For each trait, we discovered novel regulators without prior functional annotations. The functional effects of the novel candidates were then validated experimentally, providing solid evidence for their roles in the respective traits. Hence, we conclude that iTARGEX can reliably identify novel factors involved in given biological traits. As such, it is capable of converting genome-wide observations into causal gene function predictions. Further application of iTARGEX in other contexts is expected to facilitate the discovery of new regulators and provide observations for novel mechanistic hypotheses regarding different biological traits and phenotypes.
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spelling pubmed-82879572021-07-19 iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover Huang, Jia-Hsin Liao, You-Rou Lin, Tzu-Chieh Tsai, Cheng-Hung Lai, Wei-Yun Chou, Yang-Kai Leu, Jun-Yi Tsai, Huai-Kuang Kao, Cheng-Fu Nucleic Acids Res Computational Biology Integrating omics data with quantification of biological traits provides unparalleled opportunities for discovery of genetic regulators by in silico inference. However, current approaches to analyze genetic-perturbation screens are limited by their reliance on annotation libraries for prioritization of hits and subsequent targeted experimentation. Here, we present iTARGEX (identification of Trait-Associated Regulatory Genes via mixture regression using EXpectation maximization), an association framework with no requirement of a priori knowledge of gene function. After creating this tool, we used it to test associations between gene expression profiles and two biological traits in single-gene deletion budding yeast mutants, including transcription homeostasis during S phase and global protein turnover. For each trait, we discovered novel regulators without prior functional annotations. The functional effects of the novel candidates were then validated experimentally, providing solid evidence for their roles in the respective traits. Hence, we conclude that iTARGEX can reliably identify novel factors involved in given biological traits. As such, it is capable of converting genome-wide observations into causal gene function predictions. Further application of iTARGEX in other contexts is expected to facilitate the discovery of new regulators and provide observations for novel mechanistic hypotheses regarding different biological traits and phenotypes. Oxford University Press 2021-07-01 /pmc/articles/PMC8287957/ /pubmed/34197604 http://dx.doi.org/10.1093/nar/gkab555 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Computational Biology
Huang, Jia-Hsin
Liao, You-Rou
Lin, Tzu-Chieh
Tsai, Cheng-Hung
Lai, Wei-Yun
Chou, Yang-Kai
Leu, Jun-Yi
Tsai, Huai-Kuang
Kao, Cheng-Fu
iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover
title iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover
title_full iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover
title_fullStr iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover
title_full_unstemmed iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover
title_short iTARGEX analysis of yeast deletome reveals novel regulators of transcriptional buffering in S phase and protein turnover
title_sort itargex analysis of yeast deletome reveals novel regulators of transcriptional buffering in s phase and protein turnover
topic Computational Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287957/
https://www.ncbi.nlm.nih.gov/pubmed/34197604
http://dx.doi.org/10.1093/nar/gkab555
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