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Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes

BACKGROUND: Reversible protein acetylation occurring on Lys-N(e) has emerged as a key regulatory post-translational modification in eukaryotes. It is mediated by two groups of enzymes: lysine acetyltransferases (KATs) and lysine deacetylases (KDACs) that catalyze the addition and removal of acetyl g...

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Autores principales: Uhrig, R. Glen, Schläpfer, Pascal, Mehta, Devang, Hirsch-Hoffmann, Matthias, Gruissem, Wilhelm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499015/
https://www.ncbi.nlm.nih.gov/pubmed/28679357
http://dx.doi.org/10.1186/s12864-017-3894-0
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author Uhrig, R. Glen
Schläpfer, Pascal
Mehta, Devang
Hirsch-Hoffmann, Matthias
Gruissem, Wilhelm
author_facet Uhrig, R. Glen
Schläpfer, Pascal
Mehta, Devang
Hirsch-Hoffmann, Matthias
Gruissem, Wilhelm
author_sort Uhrig, R. Glen
collection PubMed
description BACKGROUND: Reversible protein acetylation occurring on Lys-N(e) has emerged as a key regulatory post-translational modification in eukaryotes. It is mediated by two groups of enzymes: lysine acetyltransferases (KATs) and lysine deacetylases (KDACs) that catalyze the addition and removal of acetyl groups from target proteins. Estimates indicate that protein acetylation is second to protein phosphorylation in abundance, with thousands of acetylated sites now identified in different subcellular compartments. Considering the important regulatory role of protein phosphorylation, elucidating the diversity of KATs and KDACs across photosynthetic eukaryotes is essential in furthering our understanding of the impact of reversible protein acetylation on plant cell processes. RESULTS: We report a genome-scale analysis of lysine acetyltransferase (KAT)- and lysine deacetylase (KDAC)-families from 53 photosynthetic eukaryotes. KAT and KDAC orthologs were identified in sequenced genomes ranging from glaucophytes and algae to land plants and then analyzed for evolutionary relationships. Based on consensus molecular phylogenetic and subcellular localization data we found new sub-classes of enzymes in established KAT- and KDAC-families. Specifically, we identified a non-photosynthetic origin of the HD-tuin family KDACs, a new monocot-specific Class I HDA-family sub-class, and a phylogenetically distinct Class II algal/heterokont sub-class which maintains an ankyrin domain not conserved in land plant Class II KDACs. Protein structure analysis showed that HDA- and SRT-KDACs exist as bare catalytic subunits with highly conserved median protein length, while all KATs maintained auxiliary domains, with CBP- and TAF(II)250-KATs displaying protein domain gain and loss over the course of photosynthetic eukaryote evolution in addition to variable protein length. Lastly, promoter element enrichment analyses across species revealed conserved cis-regulatory sequences that support KAT and KDAC involvement in the regulation of plant development, cold/drought stress response, as well as cellular processes such as the circadian clock. CONCLUSIONS: Our results reveal new evolutionary, structural, and biological insights into the KAT- and KDAC-families of photosynthetic eukaryotes, including evolutionary parallels to protein kinases and protein phosphatases. Further, we provide a comprehensive annotation framework through our extensive phylogenetic analysis, from which future research investigating aspects of protein acetylation in plants can use to position new findings in a broader context. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3894-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-54990152017-07-10 Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes Uhrig, R. Glen Schläpfer, Pascal Mehta, Devang Hirsch-Hoffmann, Matthias Gruissem, Wilhelm BMC Genomics Research Article BACKGROUND: Reversible protein acetylation occurring on Lys-N(e) has emerged as a key regulatory post-translational modification in eukaryotes. It is mediated by two groups of enzymes: lysine acetyltransferases (KATs) and lysine deacetylases (KDACs) that catalyze the addition and removal of acetyl groups from target proteins. Estimates indicate that protein acetylation is second to protein phosphorylation in abundance, with thousands of acetylated sites now identified in different subcellular compartments. Considering the important regulatory role of protein phosphorylation, elucidating the diversity of KATs and KDACs across photosynthetic eukaryotes is essential in furthering our understanding of the impact of reversible protein acetylation on plant cell processes. RESULTS: We report a genome-scale analysis of lysine acetyltransferase (KAT)- and lysine deacetylase (KDAC)-families from 53 photosynthetic eukaryotes. KAT and KDAC orthologs were identified in sequenced genomes ranging from glaucophytes and algae to land plants and then analyzed for evolutionary relationships. Based on consensus molecular phylogenetic and subcellular localization data we found new sub-classes of enzymes in established KAT- and KDAC-families. Specifically, we identified a non-photosynthetic origin of the HD-tuin family KDACs, a new monocot-specific Class I HDA-family sub-class, and a phylogenetically distinct Class II algal/heterokont sub-class which maintains an ankyrin domain not conserved in land plant Class II KDACs. Protein structure analysis showed that HDA- and SRT-KDACs exist as bare catalytic subunits with highly conserved median protein length, while all KATs maintained auxiliary domains, with CBP- and TAF(II)250-KATs displaying protein domain gain and loss over the course of photosynthetic eukaryote evolution in addition to variable protein length. Lastly, promoter element enrichment analyses across species revealed conserved cis-regulatory sequences that support KAT and KDAC involvement in the regulation of plant development, cold/drought stress response, as well as cellular processes such as the circadian clock. CONCLUSIONS: Our results reveal new evolutionary, structural, and biological insights into the KAT- and KDAC-families of photosynthetic eukaryotes, including evolutionary parallels to protein kinases and protein phosphatases. Further, we provide a comprehensive annotation framework through our extensive phylogenetic analysis, from which future research investigating aspects of protein acetylation in plants can use to position new findings in a broader context. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3894-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-05 /pmc/articles/PMC5499015/ /pubmed/28679357 http://dx.doi.org/10.1186/s12864-017-3894-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Uhrig, R. Glen
Schläpfer, Pascal
Mehta, Devang
Hirsch-Hoffmann, Matthias
Gruissem, Wilhelm
Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
title Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
title_full Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
title_fullStr Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
title_full_unstemmed Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
title_short Genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
title_sort genome-scale analysis of regulatory protein acetylation enzymes from photosynthetic eukaryotes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499015/
https://www.ncbi.nlm.nih.gov/pubmed/28679357
http://dx.doi.org/10.1186/s12864-017-3894-0
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