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Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals

Heat shock protein 70 (Hsp70) is a molecular chaperone providing tolerance to heat and other challenges at the cellular and organismal levels. We sequenced a genomic cluster containing three hsp70 family genes linked with major histocompatibility complex (MHC) class III region from an extremely heat...

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Autores principales: Garbuz, David G., Astakhova, Lubov N., Zatsepina, Olga G., Arkhipova, Irina R., Nudler, Eugene, Evgen'ev, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212538/
https://www.ncbi.nlm.nih.gov/pubmed/22096537
http://dx.doi.org/10.1371/journal.pone.0027205
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author Garbuz, David G.
Astakhova, Lubov N.
Zatsepina, Olga G.
Arkhipova, Irina R.
Nudler, Eugene
Evgen'ev, Michael B.
author_facet Garbuz, David G.
Astakhova, Lubov N.
Zatsepina, Olga G.
Arkhipova, Irina R.
Nudler, Eugene
Evgen'ev, Michael B.
author_sort Garbuz, David G.
collection PubMed
description Heat shock protein 70 (Hsp70) is a molecular chaperone providing tolerance to heat and other challenges at the cellular and organismal levels. We sequenced a genomic cluster containing three hsp70 family genes linked with major histocompatibility complex (MHC) class III region from an extremely heat tolerant animal, camel (Camelus dromedarius). Two hsp70 family genes comprising the cluster contain heat shock elements (HSEs), while the third gene lacks HSEs and should not be induced by heat shock. Comparison of the camel hsp70 cluster with the corresponding regions from several mammalian species revealed similar organization of genes forming the cluster. Specifically, the two heat inducible hsp70 genes are arranged in tandem, while the third constitutively expressed hsp70 family member is present in inverted orientation. Comparison of regulatory regions of hsp70 genes from camel and other mammals demonstrates that transcription factor matches with highest significance are located in the highly conserved 250-bp upstream region and correspond to HSEs followed by NF-Y and Sp1 binding sites. The high degree of sequence conservation leaves little room for putative camel-specific regulatory elements. Surprisingly, RT-PCR and 5′/3′-RACE analysis demonstrated that all three hsp70 genes are expressed in camel's muscle and blood cells not only after heat shock, but under normal physiological conditions as well, and may account for tolerance of camel cells to extreme environmental conditions. A high degree of evolutionary conservation observed for the hsp70 cluster always linked with MHC locus in mammals suggests an important role of such organization for coordinated functioning of these vital genes.
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spelling pubmed-32125382011-11-17 Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals Garbuz, David G. Astakhova, Lubov N. Zatsepina, Olga G. Arkhipova, Irina R. Nudler, Eugene Evgen'ev, Michael B. PLoS One Research Article Heat shock protein 70 (Hsp70) is a molecular chaperone providing tolerance to heat and other challenges at the cellular and organismal levels. We sequenced a genomic cluster containing three hsp70 family genes linked with major histocompatibility complex (MHC) class III region from an extremely heat tolerant animal, camel (Camelus dromedarius). Two hsp70 family genes comprising the cluster contain heat shock elements (HSEs), while the third gene lacks HSEs and should not be induced by heat shock. Comparison of the camel hsp70 cluster with the corresponding regions from several mammalian species revealed similar organization of genes forming the cluster. Specifically, the two heat inducible hsp70 genes are arranged in tandem, while the third constitutively expressed hsp70 family member is present in inverted orientation. Comparison of regulatory regions of hsp70 genes from camel and other mammals demonstrates that transcription factor matches with highest significance are located in the highly conserved 250-bp upstream region and correspond to HSEs followed by NF-Y and Sp1 binding sites. The high degree of sequence conservation leaves little room for putative camel-specific regulatory elements. Surprisingly, RT-PCR and 5′/3′-RACE analysis demonstrated that all three hsp70 genes are expressed in camel's muscle and blood cells not only after heat shock, but under normal physiological conditions as well, and may account for tolerance of camel cells to extreme environmental conditions. A high degree of evolutionary conservation observed for the hsp70 cluster always linked with MHC locus in mammals suggests an important role of such organization for coordinated functioning of these vital genes. Public Library of Science 2011-11-09 /pmc/articles/PMC3212538/ /pubmed/22096537 http://dx.doi.org/10.1371/journal.pone.0027205 Text en Garbuz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Garbuz, David G.
Astakhova, Lubov N.
Zatsepina, Olga G.
Arkhipova, Irina R.
Nudler, Eugene
Evgen'ev, Michael B.
Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals
title Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals
title_full Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals
title_fullStr Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals
title_full_unstemmed Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals
title_short Functional Organization of hsp70 Cluster in Camel (Camelus dromedarius) and Other Mammals
title_sort functional organization of hsp70 cluster in camel (camelus dromedarius) and other mammals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212538/
https://www.ncbi.nlm.nih.gov/pubmed/22096537
http://dx.doi.org/10.1371/journal.pone.0027205
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