Trypanosoma brucei: Frequent loss of a telomeric variant surface glycoprotein gene

We have observed the loss of an inactive telomeric variant surface glycoprotein (VSG) gene that is located on a minichromosome in Trypanosoma brucei. If this is due to gene conversion, it is the third “silent” gene conversion (i.e., one that does not produce an antigenic switch) detected in 19 antig...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Experimental parasitology 1989, Vol.68 (1), p.8-16
Hauptverfasser: Aline, Robert F., Myler, Peter J., Stuart, Kenneth D.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 16
container_issue 1
container_start_page 8
container_title Experimental parasitology
container_volume 68
creator Aline, Robert F.
Myler, Peter J.
Stuart, Kenneth D.
description We have observed the loss of an inactive telomeric variant surface glycoprotein (VSG) gene that is located on a minichromosome in Trypanosoma brucei. If this is due to gene conversion, it is the third “silent” gene conversion (i.e., one that does not produce an antigenic switch) detected in 19 antigenic switches of the IsTaR 1 serodeme. This is suprisingly frequent since the immune response cannot select against the inactive gene. We estimate that 10 −1 to 10 −3 telomeric VSG gene conversions occur per generation, which is at least 100 times more frequent than antigenic switching. Since all three “silent” gene conversions involved an IsTat 5 VSG gene, the frequency may vary among telomeric VSG genes. However, the high gene conversion frequency for the 5 VSG gene does not ensure a higher antigenic switch frequency than other telomeric VSG genes for which we have probes. These results suggest that gene conversion rapidly alters the repertoire of telomeric VSG genes, possibly including those on minichromosomes, producing a continual variation in the VSG genes that are more likely to be expressed.
doi_str_mv 10.1016/0014-4894(89)90003-9
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78870978</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0014489489900039</els_id><sourcerecordid>15199839</sourcerecordid><originalsourceid>FETCH-LOGICAL-c417t-5a48cb2f0262aa55731c00a408ea559a6c88b5ebd895e1e09cf34e8a1e824d8f3</originalsourceid><addsrcrecordid>eNqFkE1r3DAQhkVJSLZp_0ELOoTSHtxqZHkt5VAIIR-FQKGkZzGWx0HFtjaSHdh_Hzm77DE9CfE-M3r1MPYJxHcQsP4hBKhCaaO-avPNCCHKwrxjKxBGFFIpc8RWB-SUvU_pX2Y0SHXCTqSBel3Civ15iNsNjiGFAXkTZ0f-gt9EepppnHgfUuKh48gn6sNA0Tv-jNFjztIcO3TEH_utC5sYJvIjf6SRPrDjDvtEH_fnGft7c_1wdVfc_779dXV5XzgF9VRUqLRrZCfkWiJWVV2CEwKV0JRvBtdO66aiptWmIiBhXFcq0gikpWp1V56xL7u9-fFcN0128MlR3-NIYU621roWptb_BaECY3RpMqh2oIv545E6u4l-wLi1IOzi3C5C7SLUamNfndtl7PN-_9wM1B6G9pJzfr7PMTnsu4ij8-mA1bKUAEvNnzuMsrRnT9Em52l01PpIbrJt8G_3eAEn_J1k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15199839</pqid></control><display><type>article</type><title>Trypanosoma brucei: Frequent loss of a telomeric variant surface glycoprotein gene</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Aline, Robert F. ; Myler, Peter J. ; Stuart, Kenneth D.</creator><creatorcontrib>Aline, Robert F. ; Myler, Peter J. ; Stuart, Kenneth D.</creatorcontrib><description>We have observed the loss of an inactive telomeric variant surface glycoprotein (VSG) gene that is located on a minichromosome in Trypanosoma brucei. If this is due to gene conversion, it is the third “silent” gene conversion (i.e., one that does not produce an antigenic switch) detected in 19 antigenic switches of the IsTaR 1 serodeme. This is suprisingly frequent since the immune response cannot select against the inactive gene. We estimate that 10 −1 to 10 −3 telomeric VSG gene conversions occur per generation, which is at least 100 times more frequent than antigenic switching. Since all three “silent” gene conversions involved an IsTat 5 VSG gene, the frequency may vary among telomeric VSG genes. However, the high gene conversion frequency for the 5 VSG gene does not ensure a higher antigenic switch frequency than other telomeric VSG genes for which we have probes. These results suggest that gene conversion rapidly alters the repertoire of telomeric VSG genes, possibly including those on minichromosomes, producing a continual variation in the VSG genes that are more likely to be expressed.</description><identifier>ISSN: 0014-4894</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1016/0014-4894(89)90003-9</identifier><identifier>PMID: 2917631</identifier><identifier>CODEN: EXPAAA</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Animals ; Antigenic Variation ; Antigens, Protozoan - genetics ; Antigens, Protozoan - immunology ; Biological and medical sciences ; Chromosomes ; Clone Cells ; Gene Conversion ; Genes ; Human protozoal diseases ; Infectious diseases ; Medical sciences ; Mice ; Parasitic diseases ; Protozoal diseases ; Restriction Mapping ; Tropical medicine ; Trypanosoma brucei ; Trypanosoma brucei brucei - genetics ; Trypanosoma brucei brucei - immunology ; Trypanosomiasis ; Variant Surface Glycoproteins, Trypanosoma - genetics ; Variant Surface Glycoproteins, Trypanosoma - immunology</subject><ispartof>Experimental parasitology, 1989, Vol.68 (1), p.8-16</ispartof><rights>1989</rights><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-5a48cb2f0262aa55731c00a408ea559a6c88b5ebd895e1e09cf34e8a1e824d8f3</citedby><cites>FETCH-LOGICAL-c417t-5a48cb2f0262aa55731c00a408ea559a6c88b5ebd895e1e09cf34e8a1e824d8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0014-4894(89)90003-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=7232118$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2917631$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aline, Robert F.</creatorcontrib><creatorcontrib>Myler, Peter J.</creatorcontrib><creatorcontrib>Stuart, Kenneth D.</creatorcontrib><title>Trypanosoma brucei: Frequent loss of a telomeric variant surface glycoprotein gene</title><title>Experimental parasitology</title><addtitle>Exp Parasitol</addtitle><description>We have observed the loss of an inactive telomeric variant surface glycoprotein (VSG) gene that is located on a minichromosome in Trypanosoma brucei. If this is due to gene conversion, it is the third “silent” gene conversion (i.e., one that does not produce an antigenic switch) detected in 19 antigenic switches of the IsTaR 1 serodeme. This is suprisingly frequent since the immune response cannot select against the inactive gene. We estimate that 10 −1 to 10 −3 telomeric VSG gene conversions occur per generation, which is at least 100 times more frequent than antigenic switching. Since all three “silent” gene conversions involved an IsTat 5 VSG gene, the frequency may vary among telomeric VSG genes. However, the high gene conversion frequency for the 5 VSG gene does not ensure a higher antigenic switch frequency than other telomeric VSG genes for which we have probes. These results suggest that gene conversion rapidly alters the repertoire of telomeric VSG genes, possibly including those on minichromosomes, producing a continual variation in the VSG genes that are more likely to be expressed.</description><subject>Animals</subject><subject>Antigenic Variation</subject><subject>Antigens, Protozoan - genetics</subject><subject>Antigens, Protozoan - immunology</subject><subject>Biological and medical sciences</subject><subject>Chromosomes</subject><subject>Clone Cells</subject><subject>Gene Conversion</subject><subject>Genes</subject><subject>Human protozoal diseases</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Parasitic diseases</subject><subject>Protozoal diseases</subject><subject>Restriction Mapping</subject><subject>Tropical medicine</subject><subject>Trypanosoma brucei</subject><subject>Trypanosoma brucei brucei - genetics</subject><subject>Trypanosoma brucei brucei - immunology</subject><subject>Trypanosomiasis</subject><subject>Variant Surface Glycoproteins, Trypanosoma - genetics</subject><subject>Variant Surface Glycoproteins, Trypanosoma - immunology</subject><issn>0014-4894</issn><issn>1090-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1r3DAQhkVJSLZp_0ELOoTSHtxqZHkt5VAIIR-FQKGkZzGWx0HFtjaSHdh_Hzm77DE9CfE-M3r1MPYJxHcQsP4hBKhCaaO-avPNCCHKwrxjKxBGFFIpc8RWB-SUvU_pX2Y0SHXCTqSBel3Civ15iNsNjiGFAXkTZ0f-gt9EepppnHgfUuKh48gn6sNA0Tv-jNFjztIcO3TEH_utC5sYJvIjf6SRPrDjDvtEH_fnGft7c_1wdVfc_779dXV5XzgF9VRUqLRrZCfkWiJWVV2CEwKV0JRvBtdO66aiptWmIiBhXFcq0gikpWp1V56xL7u9-fFcN0128MlR3-NIYU621roWptb_BaECY3RpMqh2oIv545E6u4l-wLi1IOzi3C5C7SLUamNfndtl7PN-_9wM1B6G9pJzfr7PMTnsu4ij8-mA1bKUAEvNnzuMsrRnT9Em52l01PpIbrJt8G_3eAEn_J1k</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>Aline, Robert F.</creator><creator>Myler, Peter J.</creator><creator>Stuart, Kenneth D.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>1989</creationdate><title>Trypanosoma brucei: Frequent loss of a telomeric variant surface glycoprotein gene</title><author>Aline, Robert F. ; Myler, Peter J. ; Stuart, Kenneth D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-5a48cb2f0262aa55731c00a408ea559a6c88b5ebd895e1e09cf34e8a1e824d8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Antigenic Variation</topic><topic>Antigens, Protozoan - genetics</topic><topic>Antigens, Protozoan - immunology</topic><topic>Biological and medical sciences</topic><topic>Chromosomes</topic><topic>Clone Cells</topic><topic>Gene Conversion</topic><topic>Genes</topic><topic>Human protozoal diseases</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Parasitic diseases</topic><topic>Protozoal diseases</topic><topic>Restriction Mapping</topic><topic>Tropical medicine</topic><topic>Trypanosoma brucei</topic><topic>Trypanosoma brucei brucei - genetics</topic><topic>Trypanosoma brucei brucei - immunology</topic><topic>Trypanosomiasis</topic><topic>Variant Surface Glycoproteins, Trypanosoma - genetics</topic><topic>Variant Surface Glycoproteins, Trypanosoma - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aline, Robert F.</creatorcontrib><creatorcontrib>Myler, Peter J.</creatorcontrib><creatorcontrib>Stuart, Kenneth D.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aline, Robert F.</au><au>Myler, Peter J.</au><au>Stuart, Kenneth D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trypanosoma brucei: Frequent loss of a telomeric variant surface glycoprotein gene</atitle><jtitle>Experimental parasitology</jtitle><addtitle>Exp Parasitol</addtitle><date>1989</date><risdate>1989</risdate><volume>68</volume><issue>1</issue><spage>8</spage><epage>16</epage><pages>8-16</pages><issn>0014-4894</issn><eissn>1090-2449</eissn><coden>EXPAAA</coden><abstract>We have observed the loss of an inactive telomeric variant surface glycoprotein (VSG) gene that is located on a minichromosome in Trypanosoma brucei. If this is due to gene conversion, it is the third “silent” gene conversion (i.e., one that does not produce an antigenic switch) detected in 19 antigenic switches of the IsTaR 1 serodeme. This is suprisingly frequent since the immune response cannot select against the inactive gene. We estimate that 10 −1 to 10 −3 telomeric VSG gene conversions occur per generation, which is at least 100 times more frequent than antigenic switching. Since all three “silent” gene conversions involved an IsTat 5 VSG gene, the frequency may vary among telomeric VSG genes. However, the high gene conversion frequency for the 5 VSG gene does not ensure a higher antigenic switch frequency than other telomeric VSG genes for which we have probes. These results suggest that gene conversion rapidly alters the repertoire of telomeric VSG genes, possibly including those on minichromosomes, producing a continual variation in the VSG genes that are more likely to be expressed.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>2917631</pmid><doi>10.1016/0014-4894(89)90003-9</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0014-4894
ispartof Experimental parasitology, 1989, Vol.68 (1), p.8-16
issn 0014-4894
1090-2449
language eng
recordid cdi_proquest_miscellaneous_78870978
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Antigenic Variation
Antigens, Protozoan - genetics
Antigens, Protozoan - immunology
Biological and medical sciences
Chromosomes
Clone Cells
Gene Conversion
Genes
Human protozoal diseases
Infectious diseases
Medical sciences
Mice
Parasitic diseases
Protozoal diseases
Restriction Mapping
Tropical medicine
Trypanosoma brucei
Trypanosoma brucei brucei - genetics
Trypanosoma brucei brucei - immunology
Trypanosomiasis
Variant Surface Glycoproteins, Trypanosoma - genetics
Variant Surface Glycoproteins, Trypanosoma - immunology
title Trypanosoma brucei: Frequent loss of a telomeric variant surface glycoprotein gene
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T19%3A36%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Trypanosoma%20brucei:%20Frequent%20loss%20of%20a%20telomeric%20variant%20surface%20glycoprotein%20gene&rft.jtitle=Experimental%20parasitology&rft.au=Aline,%20Robert%20F.&rft.date=1989&rft.volume=68&rft.issue=1&rft.spage=8&rft.epage=16&rft.pages=8-16&rft.issn=0014-4894&rft.eissn=1090-2449&rft.coden=EXPAAA&rft_id=info:doi/10.1016/0014-4894(89)90003-9&rft_dat=%3Cproquest_cross%3E15199839%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=15199839&rft_id=info:pmid/2917631&rft_els_id=0014489489900039&rfr_iscdi=true