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Yeast-Based Genetic Interaction Analysis of Human Kinome
Kinases are critical intracellular signaling proteins. To better understand kinase-mediated signal transduction, a large-scale human–yeast genetic interaction screen was performed. Among 597 human kinase genes tested, 28 displayed strong toxicity in yeast when overexpressed. En masse transformation...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291280/ https://www.ncbi.nlm.nih.gov/pubmed/32392905 http://dx.doi.org/10.3390/cells9051156 |
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author | Kim, Jae-Hong Seo, Yeojin Jo, Myungjin Jeon, Hyejin Lee, Won-Ha Yachie, Nozomu Zhong, Quan Vidal, Marc Roth, Frederick P. Suk, Kyoungho |
author_facet | Kim, Jae-Hong Seo, Yeojin Jo, Myungjin Jeon, Hyejin Lee, Won-Ha Yachie, Nozomu Zhong, Quan Vidal, Marc Roth, Frederick P. Suk, Kyoungho |
author_sort | Kim, Jae-Hong |
collection | PubMed |
description | Kinases are critical intracellular signaling proteins. To better understand kinase-mediated signal transduction, a large-scale human–yeast genetic interaction screen was performed. Among 597 human kinase genes tested, 28 displayed strong toxicity in yeast when overexpressed. En masse transformation of these toxic kinase genes into 4653 homozygous diploid yeast deletion mutants followed by barcode sequencing identified yeast toxicity modifiers and thus their human orthologs. Subsequent network analyses and functional grouping revealed that the 28 kinases and their 676 interaction partners (corresponding to a total of 969 genetic interactions) are enriched in cell death and survival (34%), small-molecule biochemistry (18%) and molecular transport (11%), among others. In the subnetwork analyses, a few kinases were commonly associated with glioma, cell migration and cell death/survival. Our analysis enabled the creation of a first draft of the kinase genetic interactome network and identified multiple drug targets for inflammatory diseases and cancer, in which deregulated kinase signaling plays a pathogenic role. |
format | Online Article Text |
id | pubmed-7291280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72912802020-06-17 Yeast-Based Genetic Interaction Analysis of Human Kinome Kim, Jae-Hong Seo, Yeojin Jo, Myungjin Jeon, Hyejin Lee, Won-Ha Yachie, Nozomu Zhong, Quan Vidal, Marc Roth, Frederick P. Suk, Kyoungho Cells Article Kinases are critical intracellular signaling proteins. To better understand kinase-mediated signal transduction, a large-scale human–yeast genetic interaction screen was performed. Among 597 human kinase genes tested, 28 displayed strong toxicity in yeast when overexpressed. En masse transformation of these toxic kinase genes into 4653 homozygous diploid yeast deletion mutants followed by barcode sequencing identified yeast toxicity modifiers and thus their human orthologs. Subsequent network analyses and functional grouping revealed that the 28 kinases and their 676 interaction partners (corresponding to a total of 969 genetic interactions) are enriched in cell death and survival (34%), small-molecule biochemistry (18%) and molecular transport (11%), among others. In the subnetwork analyses, a few kinases were commonly associated with glioma, cell migration and cell death/survival. Our analysis enabled the creation of a first draft of the kinase genetic interactome network and identified multiple drug targets for inflammatory diseases and cancer, in which deregulated kinase signaling plays a pathogenic role. MDPI 2020-05-07 /pmc/articles/PMC7291280/ /pubmed/32392905 http://dx.doi.org/10.3390/cells9051156 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Jae-Hong Seo, Yeojin Jo, Myungjin Jeon, Hyejin Lee, Won-Ha Yachie, Nozomu Zhong, Quan Vidal, Marc Roth, Frederick P. Suk, Kyoungho Yeast-Based Genetic Interaction Analysis of Human Kinome |
title | Yeast-Based Genetic Interaction Analysis of Human Kinome |
title_full | Yeast-Based Genetic Interaction Analysis of Human Kinome |
title_fullStr | Yeast-Based Genetic Interaction Analysis of Human Kinome |
title_full_unstemmed | Yeast-Based Genetic Interaction Analysis of Human Kinome |
title_short | Yeast-Based Genetic Interaction Analysis of Human Kinome |
title_sort | yeast-based genetic interaction analysis of human kinome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291280/ https://www.ncbi.nlm.nih.gov/pubmed/32392905 http://dx.doi.org/10.3390/cells9051156 |
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