Cargando…

A subcellular map of the human kinome

The human kinome comprises 538 kinases playing essential functions by catalyzing protein phosphorylation. Annotation of subcellular distribution of the kinome greatly facilitates investigation of normal and disease mechanisms. Here, we present Kinome Atlas (KA), an image-based map of the kinome anno...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Haitao, Cao, Xiaolei, Tang, Mei, Zhong, Guoxuan, Si, Yuan, Li, Haidong, Zhu, Feifeng, Liao, Qinghua, Li, Liuju, Zhao, Jianhui, Feng, Jia, Li, Shuaifeng, Wang, Chenliang, Kaulich, Manuel, Wang, Fangwei, Chen, Liangyi, Li, Li, Xia, Zongping, Liang, Tingbo, Lu, Huasong, Feng, Xin-Hua, Zhao, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175086/
https://www.ncbi.nlm.nih.gov/pubmed/33988507
http://dx.doi.org/10.7554/eLife.64943
_version_ 1783702985950363648
author Zhang, Haitao
Cao, Xiaolei
Tang, Mei
Zhong, Guoxuan
Si, Yuan
Li, Haidong
Zhu, Feifeng
Liao, Qinghua
Li, Liuju
Zhao, Jianhui
Feng, Jia
Li, Shuaifeng
Wang, Chenliang
Kaulich, Manuel
Wang, Fangwei
Chen, Liangyi
Li, Li
Xia, Zongping
Liang, Tingbo
Lu, Huasong
Feng, Xin-Hua
Zhao, Bin
author_facet Zhang, Haitao
Cao, Xiaolei
Tang, Mei
Zhong, Guoxuan
Si, Yuan
Li, Haidong
Zhu, Feifeng
Liao, Qinghua
Li, Liuju
Zhao, Jianhui
Feng, Jia
Li, Shuaifeng
Wang, Chenliang
Kaulich, Manuel
Wang, Fangwei
Chen, Liangyi
Li, Li
Xia, Zongping
Liang, Tingbo
Lu, Huasong
Feng, Xin-Hua
Zhao, Bin
author_sort Zhang, Haitao
collection PubMed
description The human kinome comprises 538 kinases playing essential functions by catalyzing protein phosphorylation. Annotation of subcellular distribution of the kinome greatly facilitates investigation of normal and disease mechanisms. Here, we present Kinome Atlas (KA), an image-based map of the kinome annotated to 10 cellular compartments. 456 epitope-tagged kinases, representing 85% of the human kinome, were expressed in HeLa cells and imaged by immunofluorescent microscopy under a similar condition. KA revealed kinase family-enriched subcellular localizations and discovered a collection of new kinase localizations at mitochondria, plasma membrane, extracellular space, and other structures. Furthermore, KA demonstrated the role of liquid-liquid phase separation in formation of kinase condensates. Identification of MOK as a mitochondrial kinase revealed its function in cristae dynamics, respiration, and oxidative stress response. Although limited by possible mislocalization due to overexpression or epitope tagging, this subcellular map of the kinome can be used to refine regulatory mechanisms involving protein phosphorylation.
format Online
Article
Text
id pubmed-8175086
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-81750862021-06-04 A subcellular map of the human kinome Zhang, Haitao Cao, Xiaolei Tang, Mei Zhong, Guoxuan Si, Yuan Li, Haidong Zhu, Feifeng Liao, Qinghua Li, Liuju Zhao, Jianhui Feng, Jia Li, Shuaifeng Wang, Chenliang Kaulich, Manuel Wang, Fangwei Chen, Liangyi Li, Li Xia, Zongping Liang, Tingbo Lu, Huasong Feng, Xin-Hua Zhao, Bin eLife Biochemistry and Chemical Biology The human kinome comprises 538 kinases playing essential functions by catalyzing protein phosphorylation. Annotation of subcellular distribution of the kinome greatly facilitates investigation of normal and disease mechanisms. Here, we present Kinome Atlas (KA), an image-based map of the kinome annotated to 10 cellular compartments. 456 epitope-tagged kinases, representing 85% of the human kinome, were expressed in HeLa cells and imaged by immunofluorescent microscopy under a similar condition. KA revealed kinase family-enriched subcellular localizations and discovered a collection of new kinase localizations at mitochondria, plasma membrane, extracellular space, and other structures. Furthermore, KA demonstrated the role of liquid-liquid phase separation in formation of kinase condensates. Identification of MOK as a mitochondrial kinase revealed its function in cristae dynamics, respiration, and oxidative stress response. Although limited by possible mislocalization due to overexpression or epitope tagging, this subcellular map of the kinome can be used to refine regulatory mechanisms involving protein phosphorylation. eLife Sciences Publications, Ltd 2021-05-14 /pmc/articles/PMC8175086/ /pubmed/33988507 http://dx.doi.org/10.7554/eLife.64943 Text en © 2021, Zhang et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
Zhang, Haitao
Cao, Xiaolei
Tang, Mei
Zhong, Guoxuan
Si, Yuan
Li, Haidong
Zhu, Feifeng
Liao, Qinghua
Li, Liuju
Zhao, Jianhui
Feng, Jia
Li, Shuaifeng
Wang, Chenliang
Kaulich, Manuel
Wang, Fangwei
Chen, Liangyi
Li, Li
Xia, Zongping
Liang, Tingbo
Lu, Huasong
Feng, Xin-Hua
Zhao, Bin
A subcellular map of the human kinome
title A subcellular map of the human kinome
title_full A subcellular map of the human kinome
title_fullStr A subcellular map of the human kinome
title_full_unstemmed A subcellular map of the human kinome
title_short A subcellular map of the human kinome
title_sort subcellular map of the human kinome
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175086/
https://www.ncbi.nlm.nih.gov/pubmed/33988507
http://dx.doi.org/10.7554/eLife.64943
work_keys_str_mv AT zhanghaitao asubcellularmapofthehumankinome
AT caoxiaolei asubcellularmapofthehumankinome
AT tangmei asubcellularmapofthehumankinome
AT zhongguoxuan asubcellularmapofthehumankinome
AT siyuan asubcellularmapofthehumankinome
AT lihaidong asubcellularmapofthehumankinome
AT zhufeifeng asubcellularmapofthehumankinome
AT liaoqinghua asubcellularmapofthehumankinome
AT liliuju asubcellularmapofthehumankinome
AT zhaojianhui asubcellularmapofthehumankinome
AT fengjia asubcellularmapofthehumankinome
AT lishuaifeng asubcellularmapofthehumankinome
AT wangchenliang asubcellularmapofthehumankinome
AT kaulichmanuel asubcellularmapofthehumankinome
AT wangfangwei asubcellularmapofthehumankinome
AT chenliangyi asubcellularmapofthehumankinome
AT lili asubcellularmapofthehumankinome
AT xiazongping asubcellularmapofthehumankinome
AT liangtingbo asubcellularmapofthehumankinome
AT luhuasong asubcellularmapofthehumankinome
AT fengxinhua asubcellularmapofthehumankinome
AT zhaobin asubcellularmapofthehumankinome
AT zhanghaitao subcellularmapofthehumankinome
AT caoxiaolei subcellularmapofthehumankinome
AT tangmei subcellularmapofthehumankinome
AT zhongguoxuan subcellularmapofthehumankinome
AT siyuan subcellularmapofthehumankinome
AT lihaidong subcellularmapofthehumankinome
AT zhufeifeng subcellularmapofthehumankinome
AT liaoqinghua subcellularmapofthehumankinome
AT liliuju subcellularmapofthehumankinome
AT zhaojianhui subcellularmapofthehumankinome
AT fengjia subcellularmapofthehumankinome
AT lishuaifeng subcellularmapofthehumankinome
AT wangchenliang subcellularmapofthehumankinome
AT kaulichmanuel subcellularmapofthehumankinome
AT wangfangwei subcellularmapofthehumankinome
AT chenliangyi subcellularmapofthehumankinome
AT lili subcellularmapofthehumankinome
AT xiazongping subcellularmapofthehumankinome
AT liangtingbo subcellularmapofthehumankinome
AT luhuasong subcellularmapofthehumankinome
AT fengxinhua subcellularmapofthehumankinome
AT zhaobin subcellularmapofthehumankinome