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Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)

Molecular chaperones, particularly the 70-kDa heat shock proteins (Hsp70s), are key orchestrators of the cellular stress response. To perform their critical functions, Hsp70s require the presence of specific co-chaperones, which include nucleotide exchange factors containing the BCL2-associated atha...

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Autores principales: Nguyen, Peter, Hess, Kyle, Smulders, Larissa, Le, Dat, Briseno, Carolina, Chavez, Christina M., Nikolaidis, Nikolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766421/
https://www.ncbi.nlm.nih.gov/pubmed/33353252
http://dx.doi.org/10.3390/ijms21249701
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author Nguyen, Peter
Hess, Kyle
Smulders, Larissa
Le, Dat
Briseno, Carolina
Chavez, Christina M.
Nikolaidis, Nikolas
author_facet Nguyen, Peter
Hess, Kyle
Smulders, Larissa
Le, Dat
Briseno, Carolina
Chavez, Christina M.
Nikolaidis, Nikolas
author_sort Nguyen, Peter
collection PubMed
description Molecular chaperones, particularly the 70-kDa heat shock proteins (Hsp70s), are key orchestrators of the cellular stress response. To perform their critical functions, Hsp70s require the presence of specific co-chaperones, which include nucleotide exchange factors containing the BCL2-associated athanogene (BAG) domain. BAG-1 is one of these proteins that function in a wide range of cellular processes, including apoptosis, protein refolding, and degradation, as well as tumorigenesis. However, the origin of BAG-1 proteins and their evolution between and within species are mostly uncharacterized. This report investigated the macro- and micro-evolution of BAG-1 using orthologous sequences and single nucleotide polymorphisms (SNPs) to elucidate the evolution and understand how natural variation affects the cellular stress response. We first collected and analyzed several BAG-1 sequences across animals, plants, and fungi; mapped intron positions and phases; reconstructed phylogeny; and analyzed protein characteristics. These data indicated that BAG-1 originated before the animals, plants, and fungi split, yet most extant fungal species have lost BAG-1. Furthermore, although BAG-1’s structure has remained relatively conserved, kingdom-specific conserved differences exist at sites of known function, suggesting functional specialization within each kingdom. We then analyzed SNPs from the 1000 genomes database to determine the evolutionary patterns within humans. These analyses revealed that the SNP density is unequally distributed within the BAG1 gene, and the ratio of non-synonymous/synonymous SNPs is significantly higher than 1 in the BAG domain region, which is an indication of positive selection. To further explore this notion, we performed several biochemical assays and found that only one out of five mutations tested altered the major co-chaperone properties of BAG-1. These data collectively suggest that although the co-chaperone functions of BAG-1 are highly conserved and can probably tolerate several radical mutations, BAG-1 might have acquired specialized and potentially unexplored functions during the evolutionary process.
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spelling pubmed-77664212020-12-28 Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1) Nguyen, Peter Hess, Kyle Smulders, Larissa Le, Dat Briseno, Carolina Chavez, Christina M. Nikolaidis, Nikolas Int J Mol Sci Article Molecular chaperones, particularly the 70-kDa heat shock proteins (Hsp70s), are key orchestrators of the cellular stress response. To perform their critical functions, Hsp70s require the presence of specific co-chaperones, which include nucleotide exchange factors containing the BCL2-associated athanogene (BAG) domain. BAG-1 is one of these proteins that function in a wide range of cellular processes, including apoptosis, protein refolding, and degradation, as well as tumorigenesis. However, the origin of BAG-1 proteins and their evolution between and within species are mostly uncharacterized. This report investigated the macro- and micro-evolution of BAG-1 using orthologous sequences and single nucleotide polymorphisms (SNPs) to elucidate the evolution and understand how natural variation affects the cellular stress response. We first collected and analyzed several BAG-1 sequences across animals, plants, and fungi; mapped intron positions and phases; reconstructed phylogeny; and analyzed protein characteristics. These data indicated that BAG-1 originated before the animals, plants, and fungi split, yet most extant fungal species have lost BAG-1. Furthermore, although BAG-1’s structure has remained relatively conserved, kingdom-specific conserved differences exist at sites of known function, suggesting functional specialization within each kingdom. We then analyzed SNPs from the 1000 genomes database to determine the evolutionary patterns within humans. These analyses revealed that the SNP density is unequally distributed within the BAG1 gene, and the ratio of non-synonymous/synonymous SNPs is significantly higher than 1 in the BAG domain region, which is an indication of positive selection. To further explore this notion, we performed several biochemical assays and found that only one out of five mutations tested altered the major co-chaperone properties of BAG-1. These data collectively suggest that although the co-chaperone functions of BAG-1 are highly conserved and can probably tolerate several radical mutations, BAG-1 might have acquired specialized and potentially unexplored functions during the evolutionary process. MDPI 2020-12-18 /pmc/articles/PMC7766421/ /pubmed/33353252 http://dx.doi.org/10.3390/ijms21249701 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
Nguyen, Peter
Hess, Kyle
Smulders, Larissa
Le, Dat
Briseno, Carolina
Chavez, Christina M.
Nikolaidis, Nikolas
Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)
title Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)
title_full Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)
title_fullStr Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)
title_full_unstemmed Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)
title_short Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1)
title_sort origin and evolution of the human bcl2-associated athanogene-1 (bag-1)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766421/
https://www.ncbi.nlm.nih.gov/pubmed/33353252
http://dx.doi.org/10.3390/ijms21249701
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