Cargando…

Contributions of substitutions and indels to the structural variations in ancient protein superfamilies

BACKGROUND: Quantitative evaluation of protein structural evolution is important for our understanding of protein biological functions and their evolutionary adaptation, and is useful in guiding protein engineering. However, compared to the models for sequence evolution, the quantitative models for...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Zheng, Wang, Jinlan, Gong, Ya, Li, Yuezhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201574/
https://www.ncbi.nlm.nih.gov/pubmed/30355304
http://dx.doi.org/10.1186/s12864-018-5178-8
_version_ 1783365533348921344
author Zhang, Zheng
Wang, Jinlan
Gong, Ya
Li, Yuezhong
author_facet Zhang, Zheng
Wang, Jinlan
Gong, Ya
Li, Yuezhong
author_sort Zhang, Zheng
collection PubMed
description BACKGROUND: Quantitative evaluation of protein structural evolution is important for our understanding of protein biological functions and their evolutionary adaptation, and is useful in guiding protein engineering. However, compared to the models for sequence evolution, the quantitative models for protein structural evolution received less attention. Ancient protein superfamilies are often considered versatile, allowing genetic and functional diversifications during long-term evolution. In this study, we investigated the quantitative impacts of sequence variations on the structural evolution of homologues in 68 ancient protein superfamilies that exist widely in sequenced eukaryotic, bacterial and archaeal genomes. RESULTS: We found that the accumulated structural variations within ancient superfamilies could be explained largely by a bilinear model that simultaneously considers amino acid substitution and insertion/deletion (indel). Both substitutions and indels are essential for explaining the structural variations within ancient superfamilies. For those ancient superfamilies with high bilinear multiple correlation coefficients, the influence of each unit of substitution or indel on structural variations is almost constant within each superfamily, but varies greatly among different superfamilies. The influence of each unit indel on structural variations is always larger than that of each unit substitution within each superfamily, but the accumulated contributions of indels to structural variations are lower than those of substitutions in most superfamilies. The total contributions of sequence indels and substitutions (46% and 54%, respectively) to the structural variations that result from sequence variations are slightly different in ancient superfamilies. CONCLUSIONS: Structural variations within ancient protein superfamilies accumulated under the significantly bilinear influence of amino acid substitutions and indels in sequences. Both substitutions and indels are essential for explaining the structural variations within ancient superfamilies. For those structural variations resulting from sequence variations, the total contribution of indels is slightly lower than that of amino acid substitutions. The regular clock exists not only in protein sequences, but also probably in protein structures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5178-8) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6201574
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-62015742018-10-31 Contributions of substitutions and indels to the structural variations in ancient protein superfamilies Zhang, Zheng Wang, Jinlan Gong, Ya Li, Yuezhong BMC Genomics Research Article BACKGROUND: Quantitative evaluation of protein structural evolution is important for our understanding of protein biological functions and their evolutionary adaptation, and is useful in guiding protein engineering. However, compared to the models for sequence evolution, the quantitative models for protein structural evolution received less attention. Ancient protein superfamilies are often considered versatile, allowing genetic and functional diversifications during long-term evolution. In this study, we investigated the quantitative impacts of sequence variations on the structural evolution of homologues in 68 ancient protein superfamilies that exist widely in sequenced eukaryotic, bacterial and archaeal genomes. RESULTS: We found that the accumulated structural variations within ancient superfamilies could be explained largely by a bilinear model that simultaneously considers amino acid substitution and insertion/deletion (indel). Both substitutions and indels are essential for explaining the structural variations within ancient superfamilies. For those ancient superfamilies with high bilinear multiple correlation coefficients, the influence of each unit of substitution or indel on structural variations is almost constant within each superfamily, but varies greatly among different superfamilies. The influence of each unit indel on structural variations is always larger than that of each unit substitution within each superfamily, but the accumulated contributions of indels to structural variations are lower than those of substitutions in most superfamilies. The total contributions of sequence indels and substitutions (46% and 54%, respectively) to the structural variations that result from sequence variations are slightly different in ancient superfamilies. CONCLUSIONS: Structural variations within ancient protein superfamilies accumulated under the significantly bilinear influence of amino acid substitutions and indels in sequences. Both substitutions and indels are essential for explaining the structural variations within ancient superfamilies. For those structural variations resulting from sequence variations, the total contribution of indels is slightly lower than that of amino acid substitutions. The regular clock exists not only in protein sequences, but also probably in protein structures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5178-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-24 /pmc/articles/PMC6201574/ /pubmed/30355304 http://dx.doi.org/10.1186/s12864-018-5178-8 Text en © The Author(s). 2018 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
Zhang, Zheng
Wang, Jinlan
Gong, Ya
Li, Yuezhong
Contributions of substitutions and indels to the structural variations in ancient protein superfamilies
title Contributions of substitutions and indels to the structural variations in ancient protein superfamilies
title_full Contributions of substitutions and indels to the structural variations in ancient protein superfamilies
title_fullStr Contributions of substitutions and indels to the structural variations in ancient protein superfamilies
title_full_unstemmed Contributions of substitutions and indels to the structural variations in ancient protein superfamilies
title_short Contributions of substitutions and indels to the structural variations in ancient protein superfamilies
title_sort contributions of substitutions and indels to the structural variations in ancient protein superfamilies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201574/
https://www.ncbi.nlm.nih.gov/pubmed/30355304
http://dx.doi.org/10.1186/s12864-018-5178-8
work_keys_str_mv AT zhangzheng contributionsofsubstitutionsandindelstothestructuralvariationsinancientproteinsuperfamilies
AT wangjinlan contributionsofsubstitutionsandindelstothestructuralvariationsinancientproteinsuperfamilies
AT gongya contributionsofsubstitutionsandindelstothestructuralvariationsinancientproteinsuperfamilies
AT liyuezhong contributionsofsubstitutionsandindelstothestructuralvariationsinancientproteinsuperfamilies