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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2011-11, Vol.6 (11), p.e27205-e27205
Hauptverfasser: Garbuz, David G, Astakhova, Lubov N, Zatsepina, Olga G, Arkhipova, Irina R, Nudler, Eugene, Evgen'ev, Michael B
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e27205
container_issue 11
container_start_page e27205
container_title PloS one
container_volume 6
creator Garbuz, David G
Astakhova, Lubov N
Zatsepina, Olga G
Arkhipova, Irina R
Nudler, Eugene
Evgen'ev, Michael B
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.
doi_str_mv 10.1371/journal.pone.0027205
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1312045447</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A476863230</galeid><doaj_id>oai_doaj_org_article_c35d699c832d4828bc94df3ff2692b66</doaj_id><sourcerecordid>A476863230</sourcerecordid><originalsourceid>FETCH-LOGICAL-c592t-225fc714372294f1e4ad36d5b12e44834eac7a177bb2cf3a94f3fce9e093f7393</originalsourceid><addsrcrecordid>eNptUsGOFCEQ7RiNu67-gVESD-phRihoaC4mm4mrm2ziRQ-eCE3DDJNuGKHbRL9e2und7JgNh4Li1at6lVdVLwleEyrIh32cUtD9-hCDXWMMAnD9qDonksKKA6aP793Pqmc57zGuacP50-oMAEteU3Fe_biaghl9LEwopq0O_o-enyg6tMsHgZHppzzahHxARg-2R-82c5gy6lIcbKeTn_J7pEOH4rgrwEEPg-7z8-qJK8G-WOJF9f3q07fNl9XN18_Xm8ublakljCuA2hlBGBUAkjlime4o7-qWgGWsocxqIzQRom3BOKoLhjpjpcWSOkElvaheH3kPfcxq2UpWhBLArGZMFMT1EdFFvVeH5AedfquovfqXKLKVTqM3vVWG1h2X0jQUOtZA0xrJutLQAZfQcl64Pi7dpraINzaMSfcnpKc_we_UNv5SFAiU9ReCtwtBij8nm0c1-Gxs3-tg45SVxDUXgshZ2Jv_kA-LW1BbXeb3wcXS1syc6pIJ3nAKFBfU-gFUOZ0dvCkOcr7kTwrYscCkmHOy7k4iwWr23-0wavafWvxXyl7dX89d0a3h6F_TJtc0</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1312045447</pqid></control><display><type>article</type><title>Functional organization of hsp70 cluster in camel (Camelus dromedarius) and other mammals</title><source>Public Library of Science (PLoS) Journals Open Access</source><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Garbuz, David G ; Astakhova, Lubov N ; Zatsepina, Olga G ; Arkhipova, Irina R ; Nudler, Eugene ; Evgen'ev, Michael B</creator><creatorcontrib>Garbuz, David G ; Astakhova, Lubov N ; Zatsepina, Olga G ; Arkhipova, Irina R ; Nudler, Eugene ; Evgen'ev, Michael B</creatorcontrib><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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0027205</identifier><identifier>PMID: 22096537</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Adaptation ; Analysis ; Animals ; Binding sites ; Biology ; Blood cells ; Blood Cells - metabolism ; Blotting, Southern ; Camelus - genetics ; Camelus - metabolism ; Camelus dromedarius ; Cloning ; Clusters ; Conservation ; Conserved sequence ; DNA, Intergenic - genetics ; Drosophila ; Environmental conditions ; Evolutionary conservation ; Functional morphology ; Genes ; Genetic aspects ; Heat ; Heat shock ; Heat shock proteins ; HSP70 Heat-Shock Proteins - genetics ; HSP70 Heat-Shock Proteins - metabolism ; Hsp70 protein ; Insects ; Laboratories ; Lupus ; Major histocompatibility complex ; Mammals ; Mammals - genetics ; Mammals - metabolism ; Molecular biology ; Multigene Family - genetics ; Muscles - metabolism ; Open Reading Frames - genetics ; Organisms ; Physiological aspects ; Polymerase chain reaction ; Regulation ; Regulatory sequences ; Reverse Transcriptase Polymerase Chain Reaction ; Sp1 protein ; Studies ; Transcription (Genetics)</subject><ispartof>PloS one, 2011-11, Vol.6 (11), p.e27205-e27205</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Garbuz et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Garbuz et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c592t-225fc714372294f1e4ad36d5b12e44834eac7a177bb2cf3a94f3fce9e093f7393</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212538/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212538/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22096537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garbuz, David G</creatorcontrib><creatorcontrib>Astakhova, Lubov N</creatorcontrib><creatorcontrib>Zatsepina, Olga G</creatorcontrib><creatorcontrib>Arkhipova, Irina R</creatorcontrib><creatorcontrib>Nudler, Eugene</creatorcontrib><creatorcontrib>Evgen'ev, Michael B</creatorcontrib><title>Functional organization of hsp70 cluster in camel (Camelus dromedarius) and other mammals</title><title>PloS one</title><addtitle>PLoS One</addtitle><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.</description><subject>Acids</subject><subject>Adaptation</subject><subject>Analysis</subject><subject>Animals</subject><subject>Binding sites</subject><subject>Biology</subject><subject>Blood cells</subject><subject>Blood Cells - metabolism</subject><subject>Blotting, Southern</subject><subject>Camelus - genetics</subject><subject>Camelus - metabolism</subject><subject>Camelus dromedarius</subject><subject>Cloning</subject><subject>Clusters</subject><subject>Conservation</subject><subject>Conserved sequence</subject><subject>DNA, Intergenic - genetics</subject><subject>Drosophila</subject><subject>Environmental conditions</subject><subject>Evolutionary conservation</subject><subject>Functional morphology</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Heat</subject><subject>Heat shock</subject><subject>Heat shock proteins</subject><subject>HSP70 Heat-Shock Proteins - genetics</subject><subject>HSP70 Heat-Shock Proteins - metabolism</subject><subject>Hsp70 protein</subject><subject>Insects</subject><subject>Laboratories</subject><subject>Lupus</subject><subject>Major histocompatibility complex</subject><subject>Mammals</subject><subject>Mammals - genetics</subject><subject>Mammals - metabolism</subject><subject>Molecular biology</subject><subject>Multigene Family - genetics</subject><subject>Muscles - metabolism</subject><subject>Open Reading Frames - genetics</subject><subject>Organisms</subject><subject>Physiological aspects</subject><subject>Polymerase chain reaction</subject><subject>Regulation</subject><subject>Regulatory sequences</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Sp1 protein</subject><subject>Studies</subject><subject>Transcription (Genetics)</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptUsGOFCEQ7RiNu67-gVESD-phRihoaC4mm4mrm2ziRQ-eCE3DDJNuGKHbRL9e2und7JgNh4Li1at6lVdVLwleEyrIh32cUtD9-hCDXWMMAnD9qDonksKKA6aP793Pqmc57zGuacP50-oMAEteU3Fe_biaghl9LEwopq0O_o-enyg6tMsHgZHppzzahHxARg-2R-82c5gy6lIcbKeTn_J7pEOH4rgrwEEPg-7z8-qJK8G-WOJF9f3q07fNl9XN18_Xm8ublakljCuA2hlBGBUAkjlime4o7-qWgGWsocxqIzQRom3BOKoLhjpjpcWSOkElvaheH3kPfcxq2UpWhBLArGZMFMT1EdFFvVeH5AedfquovfqXKLKVTqM3vVWG1h2X0jQUOtZA0xrJutLQAZfQcl64Pi7dpraINzaMSfcnpKc_we_UNv5SFAiU9ReCtwtBij8nm0c1-Gxs3-tg45SVxDUXgshZ2Jv_kA-LW1BbXeb3wcXS1syc6pIJ3nAKFBfU-gFUOZ0dvCkOcr7kTwrYscCkmHOy7k4iwWr23-0wavafWvxXyl7dX89d0a3h6F_TJtc0</recordid><startdate>20111109</startdate><enddate>20111109</enddate><creator>Garbuz, David G</creator><creator>Astakhova, Lubov N</creator><creator>Zatsepina, Olga G</creator><creator>Arkhipova, Irina R</creator><creator>Nudler, Eugene</creator><creator>Evgen'ev, Michael B</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20111109</creationdate><title>Functional organization of hsp70 cluster in camel (Camelus dromedarius) and other mammals</title><author>Garbuz, David G ; Astakhova, Lubov N ; Zatsepina, Olga G ; Arkhipova, Irina R ; Nudler, Eugene ; Evgen'ev, Michael B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c592t-225fc714372294f1e4ad36d5b12e44834eac7a177bb2cf3a94f3fce9e093f7393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acids</topic><topic>Adaptation</topic><topic>Analysis</topic><topic>Animals</topic><topic>Binding sites</topic><topic>Biology</topic><topic>Blood cells</topic><topic>Blood Cells - metabolism</topic><topic>Blotting, Southern</topic><topic>Camelus - genetics</topic><topic>Camelus - metabolism</topic><topic>Camelus dromedarius</topic><topic>Cloning</topic><topic>Clusters</topic><topic>Conservation</topic><topic>Conserved sequence</topic><topic>DNA, Intergenic - genetics</topic><topic>Drosophila</topic><topic>Environmental conditions</topic><topic>Evolutionary conservation</topic><topic>Functional morphology</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Heat</topic><topic>Heat shock</topic><topic>Heat shock proteins</topic><topic>HSP70 Heat-Shock Proteins - genetics</topic><topic>HSP70 Heat-Shock Proteins - metabolism</topic><topic>Hsp70 protein</topic><topic>Insects</topic><topic>Laboratories</topic><topic>Lupus</topic><topic>Major histocompatibility complex</topic><topic>Mammals</topic><topic>Mammals - genetics</topic><topic>Mammals - metabolism</topic><topic>Molecular biology</topic><topic>Multigene Family - genetics</topic><topic>Muscles - metabolism</topic><topic>Open Reading Frames - genetics</topic><topic>Organisms</topic><topic>Physiological aspects</topic><topic>Polymerase chain reaction</topic><topic>Regulation</topic><topic>Regulatory sequences</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Sp1 protein</topic><topic>Studies</topic><topic>Transcription (Genetics)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garbuz, David G</creatorcontrib><creatorcontrib>Astakhova, Lubov N</creatorcontrib><creatorcontrib>Zatsepina, Olga G</creatorcontrib><creatorcontrib>Arkhipova, Irina R</creatorcontrib><creatorcontrib>Nudler, Eugene</creatorcontrib><creatorcontrib>Evgen'ev, Michael B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garbuz, David G</au><au>Astakhova, Lubov N</au><au>Zatsepina, Olga G</au><au>Arkhipova, Irina R</au><au>Nudler, Eugene</au><au>Evgen'ev, Michael B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional organization of hsp70 cluster in camel (Camelus dromedarius) and other mammals</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-11-09</date><risdate>2011</risdate><volume>6</volume><issue>11</issue><spage>e27205</spage><epage>e27205</epage><pages>e27205-e27205</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22096537</pmid><doi>10.1371/journal.pone.0027205</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2011-11, Vol.6 (11), p.e27205-e27205
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1312045447
source Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Acids
Adaptation
Analysis
Animals
Binding sites
Biology
Blood cells
Blood Cells - metabolism
Blotting, Southern
Camelus - genetics
Camelus - metabolism
Camelus dromedarius
Cloning
Clusters
Conservation
Conserved sequence
DNA, Intergenic - genetics
Drosophila
Environmental conditions
Evolutionary conservation
Functional morphology
Genes
Genetic aspects
Heat
Heat shock
Heat shock proteins
HSP70 Heat-Shock Proteins - genetics
HSP70 Heat-Shock Proteins - metabolism
Hsp70 protein
Insects
Laboratories
Lupus
Major histocompatibility complex
Mammals
Mammals - genetics
Mammals - metabolism
Molecular biology
Multigene Family - genetics
Muscles - metabolism
Open Reading Frames - genetics
Organisms
Physiological aspects
Polymerase chain reaction
Regulation
Regulatory sequences
Reverse Transcriptase Polymerase Chain Reaction
Sp1 protein
Studies
Transcription (Genetics)
title Functional organization of hsp70 cluster in camel (Camelus dromedarius) and other mammals
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T17%3A02%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Functional%20organization%20of%20hsp70%20cluster%20in%20camel%20(Camelus%20dromedarius)%20and%20other%20mammals&rft.jtitle=PloS%20one&rft.au=Garbuz,%20David%20G&rft.date=2011-11-09&rft.volume=6&rft.issue=11&rft.spage=e27205&rft.epage=e27205&rft.pages=e27205-e27205&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0027205&rft_dat=%3Cgale_plos_%3EA476863230%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1312045447&rft_id=info:pmid/22096537&rft_galeid=A476863230&rft_doaj_id=oai_doaj_org_article_c35d699c832d4828bc94df3ff2692b66&rfr_iscdi=true