Expression profiling using random genomic DNA microarrays identifies differentially expressed genes associated with three major developmental stages of the protozoan parasite Leishmania major
To complete its life cycle, protozoan parasites of the genus Leishmania undergo at least three major developmental transitions. However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess...
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Veröffentlicht in: | Molecular and biochemical parasitology 2004-07, Vol.136 (1), p.71-86 |
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creator | Akopyants, Natalia S Matlib, Robin S Bukanova, Elena N Smeds, Matthew R Brownstein, Bernard H Stormo, Gary D Beverley, Stephen M |
description | To complete its life cycle, protozoan parasites of the genus Leishmania undergo at least three major developmental transitions. However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess changes in transcript abundance in three stages: replicating promastigotes and infective non-replicating metacyclics, which occur in the sand fly vector, and in the amastigote stage residing with macrophage phagolysosomes in mammals. Microarrays were developed containing 11,484 PCR products that included a number of known genes and 10,464 random 1 kb genomic DNA fragments. Arrays were hybridized in triplicate and genes showing two-fold or greater changes in 2/3 experiments were scored as differentially expressed. Remarkably, only about one percent of the DNAs expression varied by this criteria, in either stage comparison. Northern blot analysis confirmed the predicted change in mRNA abundance for most of these (68%). This set of genes included most of those previously identified in the literature as differentially regulated as well as a number of novel genes. Notably, Leishmania maxicircle transcripts showed strong up-regulation in metacyclic and amastigote parasites, probably associated with changes in parasite energy metabolism. However, current data suggest that expression profiling using shotgun DNA libraries significantly underestimates the extent of regulated transcripts. |
doi_str_mv | 10.1016/j.molbiopara.2004.03.002 |
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However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess changes in transcript abundance in three stages: replicating promastigotes and infective non-replicating metacyclics, which occur in the sand fly vector, and in the amastigote stage residing with macrophage phagolysosomes in mammals. Microarrays were developed containing 11,484 PCR products that included a number of known genes and 10,464 random 1 kb genomic DNA fragments. Arrays were hybridized in triplicate and genes showing two-fold or greater changes in 2/3 experiments were scored as differentially expressed. Remarkably, only about one percent of the DNAs expression varied by this criteria, in either stage comparison. Northern blot analysis confirmed the predicted change in mRNA abundance for most of these (68%). This set of genes included most of those previously identified in the literature as differentially regulated as well as a number of novel genes. Notably, Leishmania maxicircle transcripts showed strong up-regulation in metacyclic and amastigote parasites, probably associated with changes in parasite energy metabolism. However, current data suggest that expression profiling using shotgun DNA libraries significantly underestimates the extent of regulated transcripts.</description><identifier>ISSN: 0166-6851</identifier><identifier>DOI: 10.1016/j.molbiopara.2004.03.002</identifier><identifier>PMID: 15138069</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Animals ; Gene Expression Profiling ; Gene Expression Regulation ; Genome, Protozoan ; Leishmania major - genetics ; Leishmania major - growth & development ; Leishmania major - metabolism ; Leishmaniasis, Cutaneous - parasitology ; Life Cycle Stages ; Mice ; Mice, Inbred BALB C ; Oligonucleotide Array Sequence Analysis - methods ; Protozoan Proteins - genetics ; Protozoan Proteins - metabolism ; Transcription, Genetic</subject><ispartof>Molecular and biochemical parasitology, 2004-07, Vol.136 (1), p.71-86</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-114ca4e5e0cfff1ff1bfbaed17ceeef2ea450794d75cc4a5dad4ef9cdb814aed3</citedby><cites>FETCH-LOGICAL-c311t-114ca4e5e0cfff1ff1bfbaed17ceeef2ea450794d75cc4a5dad4ef9cdb814aed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15138069$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akopyants, Natalia S</creatorcontrib><creatorcontrib>Matlib, Robin S</creatorcontrib><creatorcontrib>Bukanova, Elena N</creatorcontrib><creatorcontrib>Smeds, Matthew R</creatorcontrib><creatorcontrib>Brownstein, Bernard H</creatorcontrib><creatorcontrib>Stormo, Gary D</creatorcontrib><creatorcontrib>Beverley, Stephen M</creatorcontrib><title>Expression profiling using random genomic DNA microarrays identifies differentially expressed genes associated with three major developmental stages of the protozoan parasite Leishmania major</title><title>Molecular and biochemical parasitology</title><addtitle>Mol Biochem Parasitol</addtitle><description>To complete its life cycle, protozoan parasites of the genus Leishmania undergo at least three major developmental transitions. However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess changes in transcript abundance in three stages: replicating promastigotes and infective non-replicating metacyclics, which occur in the sand fly vector, and in the amastigote stage residing with macrophage phagolysosomes in mammals. Microarrays were developed containing 11,484 PCR products that included a number of known genes and 10,464 random 1 kb genomic DNA fragments. Arrays were hybridized in triplicate and genes showing two-fold or greater changes in 2/3 experiments were scored as differentially expressed. Remarkably, only about one percent of the DNAs expression varied by this criteria, in either stage comparison. Northern blot analysis confirmed the predicted change in mRNA abundance for most of these (68%). This set of genes included most of those previously identified in the literature as differentially regulated as well as a number of novel genes. Notably, Leishmania maxicircle transcripts showed strong up-regulation in metacyclic and amastigote parasites, probably associated with changes in parasite energy metabolism. However, current data suggest that expression profiling using shotgun DNA libraries significantly underestimates the extent of regulated transcripts.</description><subject>Animals</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation</subject><subject>Genome, Protozoan</subject><subject>Leishmania major - genetics</subject><subject>Leishmania major - growth & development</subject><subject>Leishmania major - metabolism</subject><subject>Leishmaniasis, Cutaneous - parasitology</subject><subject>Life Cycle Stages</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Oligonucleotide Array Sequence Analysis - methods</subject><subject>Protozoan Proteins - genetics</subject><subject>Protozoan Proteins - metabolism</subject><subject>Transcription, Genetic</subject><issn>0166-6851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc9uGyEQxjm0atI0rxBx6s1b2L_2MUrTtJLVXtozmoXBxoJly-C27svl1cLKliIhRsN8v2HgY4xLUUkh-0-HKkQ_ujhDgqoWoq1EUwlRv2HXpdyv-nUnr9h7ooMQohv6_h27kp1s1qLfXLPnx39zQiIXJz6naJ13044fadkTTCYGvsMpBqf55-_3vMQUISU4EXcGp-ysQ-LGWYtpScH7E8dzTzQLW8pAFLWDXA7-urzneZ8QeYBDTNzgH_RxDgUGzynDrgDRFg0uA-X4P0IZrTyOXEa-RUf7AJODM_-BvbXgCW8v8Yb9-vL48-Hravvj6dvD_XalGynzSspWQ4sdCm2tlWWNdgQ0ctCIaGuEthPDpjVDp3ULnQHTot1oM65lW3TNDft47ltm-n1Eyio40ug9TBiPpAa5qWvRtEW4PgvLRxEltGpOLkA6KSnUYpg6qFfD1GKYEo0qhhX07nLHcQxoXsGLW80LshyhGA</recordid><startdate>200407</startdate><enddate>200407</enddate><creator>Akopyants, Natalia S</creator><creator>Matlib, Robin S</creator><creator>Bukanova, Elena N</creator><creator>Smeds, Matthew R</creator><creator>Brownstein, Bernard H</creator><creator>Stormo, Gary D</creator><creator>Beverley, Stephen M</creator><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>7X8</scope></search><sort><creationdate>200407</creationdate><title>Expression profiling using random genomic DNA microarrays identifies differentially expressed genes associated with three major developmental stages of the protozoan parasite Leishmania major</title><author>Akopyants, Natalia S ; Matlib, Robin S ; Bukanova, Elena N ; Smeds, Matthew R ; Brownstein, Bernard H ; Stormo, Gary D ; Beverley, Stephen M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-114ca4e5e0cfff1ff1bfbaed17ceeef2ea450794d75cc4a5dad4ef9cdb814aed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation</topic><topic>Genome, Protozoan</topic><topic>Leishmania major - genetics</topic><topic>Leishmania major - growth & development</topic><topic>Leishmania major - metabolism</topic><topic>Leishmaniasis, Cutaneous - parasitology</topic><topic>Life Cycle Stages</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Oligonucleotide Array Sequence Analysis - methods</topic><topic>Protozoan Proteins - genetics</topic><topic>Protozoan Proteins - metabolism</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akopyants, Natalia S</creatorcontrib><creatorcontrib>Matlib, Robin S</creatorcontrib><creatorcontrib>Bukanova, Elena N</creatorcontrib><creatorcontrib>Smeds, Matthew R</creatorcontrib><creatorcontrib>Brownstein, Bernard H</creatorcontrib><creatorcontrib>Stormo, Gary D</creatorcontrib><creatorcontrib>Beverley, Stephen M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and biochemical parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akopyants, Natalia S</au><au>Matlib, Robin S</au><au>Bukanova, Elena N</au><au>Smeds, Matthew R</au><au>Brownstein, Bernard H</au><au>Stormo, Gary D</au><au>Beverley, Stephen M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression profiling using random genomic DNA microarrays identifies differentially expressed genes associated with three major developmental stages of the protozoan parasite Leishmania major</atitle><jtitle>Molecular and biochemical parasitology</jtitle><addtitle>Mol Biochem Parasitol</addtitle><date>2004-07</date><risdate>2004</risdate><volume>136</volume><issue>1</issue><spage>71</spage><epage>86</epage><pages>71-86</pages><issn>0166-6851</issn><abstract>To complete its life cycle, protozoan parasites of the genus Leishmania undergo at least three major developmental transitions. However, previous efforts to identify genes showing stage regulated changes in transcript abundance have yielded relatively few. Here we used expression profiling to assess changes in transcript abundance in three stages: replicating promastigotes and infective non-replicating metacyclics, which occur in the sand fly vector, and in the amastigote stage residing with macrophage phagolysosomes in mammals. Microarrays were developed containing 11,484 PCR products that included a number of known genes and 10,464 random 1 kb genomic DNA fragments. Arrays were hybridized in triplicate and genes showing two-fold or greater changes in 2/3 experiments were scored as differentially expressed. Remarkably, only about one percent of the DNAs expression varied by this criteria, in either stage comparison. Northern blot analysis confirmed the predicted change in mRNA abundance for most of these (68%). This set of genes included most of those previously identified in the literature as differentially regulated as well as a number of novel genes. Notably, Leishmania maxicircle transcripts showed strong up-regulation in metacyclic and amastigote parasites, probably associated with changes in parasite energy metabolism. However, current data suggest that expression profiling using shotgun DNA libraries significantly underestimates the extent of regulated transcripts.</abstract><cop>Netherlands</cop><pmid>15138069</pmid><doi>10.1016/j.molbiopara.2004.03.002</doi><tpages>16</tpages></addata></record> |
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subjects | Animals Gene Expression Profiling Gene Expression Regulation Genome, Protozoan Leishmania major - genetics Leishmania major - growth & development Leishmania major - metabolism Leishmaniasis, Cutaneous - parasitology Life Cycle Stages Mice Mice, Inbred BALB C Oligonucleotide Array Sequence Analysis - methods Protozoan Proteins - genetics Protozoan Proteins - metabolism Transcription, Genetic |
title | Expression profiling using random genomic DNA microarrays identifies differentially expressed genes associated with three major developmental stages of the protozoan parasite Leishmania major |
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