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Karyotype determination and gene mapping in two clinical isolates of Penicillium marneffei
Electrophoretic karyotypes from two clinical isolates of Penicillium marneffei were derived using contoured-clamped homogeneous electric field (CHEF) gel electrophoresis. Five chromosome-sized DNA fragments were resolved from each isolate. Chromosomal length polymorphisms were evident among the thre...
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Published in: | Medical mycology (Oxford) 2009-01, Vol.47 (3), p.286-295 |
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description | Electrophoretic karyotypes from two clinical isolates of Penicillium marneffei were derived using contoured-clamped homogeneous electric field (CHEF) gel electrophoresis. Five chromosome-sized DNA fragments were resolved from each isolate. Chromosomal length polymorphisms were evident among the three largest molecules. Based upon these electrophoretic separation patterns, individual chromosomes were estimated to range in size from 2.0 to ≥ 6.3 Mbp with a total genome size of 20.6 to ≥ 21.6 Mbp. However, Southern blot analysis using a telomeric probe suggests that P. marneffei may possess as many as seven chromosomes, including two pairs of molecules that co-migrate under the CHEF separation conditions employed in this study. Hence, the total genome size of P. marneffei may be as large as 25.7 to ≥ 26.7 Mbp. Further hybridization analysis mapped four chitin synthase homologues to specific chromosomes as well as genes for chitinase, malate synthase, isocitrate lyase, isocitrate dehydrogenase, 5.8S rRNA, and 23S rRNA. The mapping analyses also suggested the existence of multiple chitinase gene homologues in P. marneffei. The collective results of this investigation provide additional foundations for facilitating the genetic characterization of P. marneffei and the molecular epidemiology of penicilliosis due to this fungus. |
doi_str_mv | 10.1080/13693780802291437 |
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Five chromosome-sized DNA fragments were resolved from each isolate. Chromosomal length polymorphisms were evident among the three largest molecules. Based upon these electrophoretic separation patterns, individual chromosomes were estimated to range in size from 2.0 to ≥ 6.3 Mbp with a total genome size of 20.6 to ≥ 21.6 Mbp. However, Southern blot analysis using a telomeric probe suggests that P. marneffei may possess as many as seven chromosomes, including two pairs of molecules that co-migrate under the CHEF separation conditions employed in this study. Hence, the total genome size of P. marneffei may be as large as 25.7 to ≥ 26.7 Mbp. Further hybridization analysis mapped four chitin synthase homologues to specific chromosomes as well as genes for chitinase, malate synthase, isocitrate lyase, isocitrate dehydrogenase, 5.8S rRNA, and 23S rRNA. The mapping analyses also suggested the existence of multiple chitinase gene homologues in P. marneffei. The collective results of this investigation provide additional foundations for facilitating the genetic characterization of P. marneffei and the molecular epidemiology of penicilliosis due to this fungus.</description><identifier>ISSN: 1369-3786</identifier><identifier>EISSN: 1460-2709</identifier><identifier>DOI: 10.1080/13693780802291437</identifier><identifier>PMID: 18668421</identifier><language>eng</language><publisher>UK: Informa UK Ltd</publisher><subject>Chromosome Mapping ; Chromosomes, Fungal ; DNA, Fungal - genetics ; Electrophoresis, Gel, Pulsed-Field ; Fungal Proteins - genetics ; Genes, rRNA ; Humans ; Karyotyping ; Mycoses - microbiology ; Nucleic Acid Hybridization ; Penicillium - genetics ; Penicillium - isolation & purification ; Penicillium marneffei</subject><ispartof>Medical mycology (Oxford), 2009-01, Vol.47 (3), p.286-295</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><rights>2009 ISHAM 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-29e2359810e2417d28d06d449f0faef0d85adba2e2e700fdeca9c2a2180de953</citedby><cites>FETCH-LOGICAL-c420t-29e2359810e2417d28d06d449f0faef0d85adba2e2e700fdeca9c2a2180de953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18668421$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gifford, Thomas D.</creatorcontrib><creatorcontrib>Cooper, Chester R.</creatorcontrib><title>Karyotype determination and gene mapping in two clinical isolates of Penicillium marneffei</title><title>Medical mycology (Oxford)</title><addtitle>Med Mycol</addtitle><description>Electrophoretic karyotypes from two clinical isolates of Penicillium marneffei were derived using contoured-clamped homogeneous electric field (CHEF) gel electrophoresis. Five chromosome-sized DNA fragments were resolved from each isolate. Chromosomal length polymorphisms were evident among the three largest molecules. Based upon these electrophoretic separation patterns, individual chromosomes were estimated to range in size from 2.0 to ≥ 6.3 Mbp with a total genome size of 20.6 to ≥ 21.6 Mbp. However, Southern blot analysis using a telomeric probe suggests that P. marneffei may possess as many as seven chromosomes, including two pairs of molecules that co-migrate under the CHEF separation conditions employed in this study. Hence, the total genome size of P. marneffei may be as large as 25.7 to ≥ 26.7 Mbp. Further hybridization analysis mapped four chitin synthase homologues to specific chromosomes as well as genes for chitinase, malate synthase, isocitrate lyase, isocitrate dehydrogenase, 5.8S rRNA, and 23S rRNA. The mapping analyses also suggested the existence of multiple chitinase gene homologues in P. marneffei. The collective results of this investigation provide additional foundations for facilitating the genetic characterization of P. marneffei and the molecular epidemiology of penicilliosis due to this fungus.</description><subject>Chromosome Mapping</subject><subject>Chromosomes, Fungal</subject><subject>DNA, Fungal - genetics</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>Fungal Proteins - genetics</subject><subject>Genes, rRNA</subject><subject>Humans</subject><subject>Karyotyping</subject><subject>Mycoses - microbiology</subject><subject>Nucleic Acid Hybridization</subject><subject>Penicillium - genetics</subject><subject>Penicillium - isolation & purification</subject><subject>Penicillium marneffei</subject><issn>1369-3786</issn><issn>1460-2709</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkE9r3DAQxUVp6G62_QC9BJ3aS5xKsixZ9BRC_pFAe9hTL0axRlktsuRINmW_fbTsQg-B0NM8Zn7vwTyEvlJyQUlLftBaqFq2RTKmKK_lB7SkXJCKSaI-Fl3uVQHEAp3mvCWESsXqT2hBWyFazugS_XnQaRen3QjYwARpcEFPLgasg8HPEAAPehxdeMYu4OlvxL13wfXaY5ej1xNkHC3-DWXnvHfzUPgUwFpwn9GJ1T7Dl-NcofXN9frqrnr8dXt_dflY9ZyRqWIKWN2olhJgnErDWkOE4VxZYjVYYtpGmyfNgIEkxBroteqZZrQlBlRTr9D3Q-yY4ssMeeoGl3vwXgeIc-4k54KxRu7Jb--SQlLaiFoUkB7APsWcE9huTK78teso6fbNd2-aL56zY_j8NID55zhWXYDzAxDn8b_yfh5wF2xMg96A9tOm1wm6bZxTKI2-434FmNid_A</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Gifford, Thomas D.</creator><creator>Cooper, Chester R.</creator><general>Informa UK Ltd</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>7X8</scope><scope>M7N</scope></search><sort><creationdate>20090101</creationdate><title>Karyotype determination and gene mapping in two clinical isolates of Penicillium marneffei</title><author>Gifford, Thomas D. ; Cooper, Chester R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-29e2359810e2417d28d06d449f0faef0d85adba2e2e700fdeca9c2a2180de953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Chromosome Mapping</topic><topic>Chromosomes, Fungal</topic><topic>DNA, Fungal - genetics</topic><topic>Electrophoresis, Gel, Pulsed-Field</topic><topic>Fungal Proteins - genetics</topic><topic>Genes, rRNA</topic><topic>Humans</topic><topic>Karyotyping</topic><topic>Mycoses - microbiology</topic><topic>Nucleic Acid Hybridization</topic><topic>Penicillium - genetics</topic><topic>Penicillium - isolation & purification</topic><topic>Penicillium marneffei</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gifford, Thomas D.</creatorcontrib><creatorcontrib>Cooper, Chester R.</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><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Medical mycology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gifford, Thomas D.</au><au>Cooper, Chester R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Karyotype determination and gene mapping in two clinical isolates of Penicillium marneffei</atitle><jtitle>Medical mycology (Oxford)</jtitle><addtitle>Med Mycol</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>47</volume><issue>3</issue><spage>286</spage><epage>295</epage><pages>286-295</pages><issn>1369-3786</issn><eissn>1460-2709</eissn><abstract>Electrophoretic karyotypes from two clinical isolates of Penicillium marneffei were derived using contoured-clamped homogeneous electric field (CHEF) gel electrophoresis. Five chromosome-sized DNA fragments were resolved from each isolate. Chromosomal length polymorphisms were evident among the three largest molecules. Based upon these electrophoretic separation patterns, individual chromosomes were estimated to range in size from 2.0 to ≥ 6.3 Mbp with a total genome size of 20.6 to ≥ 21.6 Mbp. However, Southern blot analysis using a telomeric probe suggests that P. marneffei may possess as many as seven chromosomes, including two pairs of molecules that co-migrate under the CHEF separation conditions employed in this study. Hence, the total genome size of P. marneffei may be as large as 25.7 to ≥ 26.7 Mbp. Further hybridization analysis mapped four chitin synthase homologues to specific chromosomes as well as genes for chitinase, malate synthase, isocitrate lyase, isocitrate dehydrogenase, 5.8S rRNA, and 23S rRNA. The mapping analyses also suggested the existence of multiple chitinase gene homologues in P. marneffei. The collective results of this investigation provide additional foundations for facilitating the genetic characterization of P. marneffei and the molecular epidemiology of penicilliosis due to this fungus.</abstract><cop>UK</cop><pub>Informa UK Ltd</pub><pmid>18668421</pmid><doi>10.1080/13693780802291437</doi><tpages>10</tpages></addata></record> |
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subjects | Chromosome Mapping Chromosomes, Fungal DNA, Fungal - genetics Electrophoresis, Gel, Pulsed-Field Fungal Proteins - genetics Genes, rRNA Humans Karyotyping Mycoses - microbiology Nucleic Acid Hybridization Penicillium - genetics Penicillium - isolation & purification Penicillium marneffei |
title | Karyotype determination and gene mapping in two clinical isolates of Penicillium marneffei |
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