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Differential expression of the NRG1 repressor controls species‐specific regulation of chlamydospore development in Candida albicans and Candida dubliniensis
Summary Candida albicans and Candida dubliniensis are opportunistic fungal pathogens that are closely related but differ in their epidemiology and in some phenotypic characteristics, including certain virulence‐related traits. A comparison of these two species at the molecular level could therefore...
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Published in: | Molecular microbiology 2005-01, Vol.55 (2), p.637-652 |
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Candida albicans and Candida dubliniensis are opportunistic fungal pathogens that are closely related but differ in their epidemiology and in some phenotypic characteristics, including certain virulence‐related traits. A comparison of these two species at the molecular level could therefore provide new insights into the biology and pathogenicity of Candida. Both species share the ability to produce chlamydospores, but only C. dubliniensis forms pseudohyphae with abundant chlamydospores on Staib agar (syn. Guizotia abyssinica creatinine agar), on which C. albicans grows as a budding yeast. To understand the basis of this species‐specific, differential regulation of morphogenetic development, we set out to identify C. albicans genes that repress chlamydospore formation under these conditions. A C. albicans genomic library was integrated into the C. dubliniensis genome and transformants were screened for clones in which filamentation and/or chlamydospore production on Staib agar was suppressed. This screen identified two genes, CaNRG1 and CaPDE2, encoding a general transcriptional repressor and a high affinity cAMP phosphodiesterase, respectively. Expression of CaNRG1 in C. dubliniensis repressed pseudohyphae and chlamydospore formation, whereas expression of CaPDE2 only reduced the extent of filamentous growth but did not affect chlamydospore formation. We found that C. dubliniensis, but not C. albicans, specifically downregulates NRG1 expression on Staib medium to allow chlamydospore development. Artificial overexpression of CdNRG1 suppressed pseudohyphal growth and production of chlamydospores in C. dubliniensis. Conversely, deletion of CaNRG1 in C. albicans resulted in chlamydospore formation on Staib agar, confirming its central role in the regulation of this morphogenetic process. Our results demonstrate that differential regulation of a single gene, NRG1, in C. albicans and C. dubliniensis is responsible for their species‐specific response to environmental signals that induce chlamydospore development. |
doi_str_mv | 10.1111/j.1365-2958.2004.04414.x |
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Candida albicans and Candida dubliniensis are opportunistic fungal pathogens that are closely related but differ in their epidemiology and in some phenotypic characteristics, including certain virulence‐related traits. A comparison of these two species at the molecular level could therefore provide new insights into the biology and pathogenicity of Candida. Both species share the ability to produce chlamydospores, but only C. dubliniensis forms pseudohyphae with abundant chlamydospores on Staib agar (syn. Guizotia abyssinica creatinine agar), on which C. albicans grows as a budding yeast. To understand the basis of this species‐specific, differential regulation of morphogenetic development, we set out to identify C. albicans genes that repress chlamydospore formation under these conditions. A C. albicans genomic library was integrated into the C. dubliniensis genome and transformants were screened for clones in which filamentation and/or chlamydospore production on Staib agar was suppressed. This screen identified two genes, CaNRG1 and CaPDE2, encoding a general transcriptional repressor and a high affinity cAMP phosphodiesterase, respectively. Expression of CaNRG1 in C. dubliniensis repressed pseudohyphae and chlamydospore formation, whereas expression of CaPDE2 only reduced the extent of filamentous growth but did not affect chlamydospore formation. We found that C. dubliniensis, but not C. albicans, specifically downregulates NRG1 expression on Staib medium to allow chlamydospore development. Artificial overexpression of CdNRG1 suppressed pseudohyphal growth and production of chlamydospores in C. dubliniensis. Conversely, deletion of CaNRG1 in C. albicans resulted in chlamydospore formation on Staib agar, confirming its central role in the regulation of this morphogenetic process. Our results demonstrate that differential regulation of a single gene, NRG1, in C. albicans and C. dubliniensis is responsible for their species‐specific response to environmental signals that induce chlamydospore development.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1111/j.1365-2958.2004.04414.x</identifier><identifier>PMID: 15659176</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Agar ; Biological and medical sciences ; Candida - genetics ; Candida - growth & development ; Candida - metabolism ; Candida - physiology ; Candida albicans - genetics ; Candida albicans - growth & development ; Candida albicans - metabolism ; Candida albicans - physiology ; Culture Media ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Gene Expression Regulation, Fungal ; Genomics ; Humans ; Microbiology ; Miscellaneous ; Molecular biology ; Mycology ; Pathogens ; Repressor Proteins - genetics ; Repressor Proteins - metabolism ; Species Specificity ; Spores, Fungal - physiology ; Yeast</subject><ispartof>Molecular microbiology, 2005-01, Vol.55 (2), p.637-652</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Jan 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4744-895a7266564884b648717b9895120bbb8218866930b1a21ef37958946346aa2d3</citedby><cites>FETCH-LOGICAL-c4744-895a7266564884b648717b9895120bbb8218866930b1a21ef37958946346aa2d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4021,27921,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16535325$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15659176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Staib, Peter</creatorcontrib><creatorcontrib>Morschhäuser, Joachim</creatorcontrib><title>Differential expression of the NRG1 repressor controls species‐specific regulation of chlamydospore development in Candida albicans and Candida dubliniensis</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><description>Summary
Candida albicans and Candida dubliniensis are opportunistic fungal pathogens that are closely related but differ in their epidemiology and in some phenotypic characteristics, including certain virulence‐related traits. A comparison of these two species at the molecular level could therefore provide new insights into the biology and pathogenicity of Candida. Both species share the ability to produce chlamydospores, but only C. dubliniensis forms pseudohyphae with abundant chlamydospores on Staib agar (syn. Guizotia abyssinica creatinine agar), on which C. albicans grows as a budding yeast. To understand the basis of this species‐specific, differential regulation of morphogenetic development, we set out to identify C. albicans genes that repress chlamydospore formation under these conditions. A C. albicans genomic library was integrated into the C. dubliniensis genome and transformants were screened for clones in which filamentation and/or chlamydospore production on Staib agar was suppressed. This screen identified two genes, CaNRG1 and CaPDE2, encoding a general transcriptional repressor and a high affinity cAMP phosphodiesterase, respectively. Expression of CaNRG1 in C. dubliniensis repressed pseudohyphae and chlamydospore formation, whereas expression of CaPDE2 only reduced the extent of filamentous growth but did not affect chlamydospore formation. We found that C. dubliniensis, but not C. albicans, specifically downregulates NRG1 expression on Staib medium to allow chlamydospore development. Artificial overexpression of CdNRG1 suppressed pseudohyphal growth and production of chlamydospores in C. dubliniensis. Conversely, deletion of CaNRG1 in C. albicans resulted in chlamydospore formation on Staib agar, confirming its central role in the regulation of this morphogenetic process. Our results demonstrate that differential regulation of a single gene, NRG1, in C. albicans and C. dubliniensis is responsible for their species‐specific response to environmental signals that induce chlamydospore development.</description><subject>Agar</subject><subject>Biological and medical sciences</subject><subject>Candida - genetics</subject><subject>Candida - growth & development</subject><subject>Candida - metabolism</subject><subject>Candida - physiology</subject><subject>Candida albicans - genetics</subject><subject>Candida albicans - growth & development</subject><subject>Candida albicans - metabolism</subject><subject>Candida albicans - physiology</subject><subject>Culture Media</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Genomics</subject><subject>Humans</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular biology</subject><subject>Mycology</subject><subject>Pathogens</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><subject>Species Specificity</subject><subject>Spores, Fungal - physiology</subject><subject>Yeast</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkc9u1DAQxi0EotvCKyALCW4J_p_kwAFtaanUgoRA4mY5jkO98trBTmD3xiPwBDwcT4KzG7USJ3ywx-PfjEffBwDEqMR5vdqUmApekIbXJUGIlYgxzMrdA7C6e3gIVqjhqKA1-XICTlPaIIQpEvQxOMFc8AZXYgV-n9u-N9H40SoHzW6IJiUbPAw9HG8NfP_xEsNoDukQoQ5-jMElmAajrUl_fv46RL3Vmfo6OTUuxfrWqe2-C2kI0cDOfDcuDNv8D7QerpXvbKegcq3VyieY73fJbmqd9db4ZNMT8KhXLpmny3kGPl-8_bR-V1x_uLxav7kuNKsYK-qGq4oIwQWra9bmvcJV2-Q0Jqht25rguhaioajFimDT0yor1DBBmVCKdPQMvDz2HWL4Npk0yq1N2jinvAlTkqLKsmb5Mvj8H3ATpujzbBI3gmNRE5Sh-gjpGFKKppdDtFsV9xIjORsoN3L2Sc4-ydlAeTBQ7nLps6X_1G5Nd1-4OJaBFwugklauj8prm-45wSmnhGfu9ZH7YZ3Z__cA8ubmao7oXzXOuLA</recordid><startdate>200501</startdate><enddate>200501</enddate><creator>Staib, Peter</creator><creator>Morschhäuser, Joachim</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Science</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200501</creationdate><title>Differential expression of the NRG1 repressor controls species‐specific regulation of chlamydospore development in Candida albicans and Candida dubliniensis</title><author>Staib, Peter ; Morschhäuser, Joachim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4744-895a7266564884b648717b9895120bbb8218866930b1a21ef37958946346aa2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Agar</topic><topic>Biological and medical sciences</topic><topic>Candida - genetics</topic><topic>Candida - growth & development</topic><topic>Candida - metabolism</topic><topic>Candida - physiology</topic><topic>Candida albicans - genetics</topic><topic>Candida albicans - growth & development</topic><topic>Candida albicans - metabolism</topic><topic>Candida albicans - physiology</topic><topic>Culture Media</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Fungal</topic><topic>Genomics</topic><topic>Humans</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular biology</topic><topic>Mycology</topic><topic>Pathogens</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>Species Specificity</topic><topic>Spores, Fungal - physiology</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Staib, Peter</creatorcontrib><creatorcontrib>Morschhäuser, Joachim</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</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>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Staib, Peter</au><au>Morschhäuser, Joachim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of the NRG1 repressor controls species‐specific regulation of chlamydospore development in Candida albicans and Candida dubliniensis</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2005-01</date><risdate>2005</risdate><volume>55</volume><issue>2</issue><spage>637</spage><epage>652</epage><pages>637-652</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary
Candida albicans and Candida dubliniensis are opportunistic fungal pathogens that are closely related but differ in their epidemiology and in some phenotypic characteristics, including certain virulence‐related traits. A comparison of these two species at the molecular level could therefore provide new insights into the biology and pathogenicity of Candida. Both species share the ability to produce chlamydospores, but only C. dubliniensis forms pseudohyphae with abundant chlamydospores on Staib agar (syn. Guizotia abyssinica creatinine agar), on which C. albicans grows as a budding yeast. To understand the basis of this species‐specific, differential regulation of morphogenetic development, we set out to identify C. albicans genes that repress chlamydospore formation under these conditions. A C. albicans genomic library was integrated into the C. dubliniensis genome and transformants were screened for clones in which filamentation and/or chlamydospore production on Staib agar was suppressed. This screen identified two genes, CaNRG1 and CaPDE2, encoding a general transcriptional repressor and a high affinity cAMP phosphodiesterase, respectively. Expression of CaNRG1 in C. dubliniensis repressed pseudohyphae and chlamydospore formation, whereas expression of CaPDE2 only reduced the extent of filamentous growth but did not affect chlamydospore formation. We found that C. dubliniensis, but not C. albicans, specifically downregulates NRG1 expression on Staib medium to allow chlamydospore development. Artificial overexpression of CdNRG1 suppressed pseudohyphal growth and production of chlamydospores in C. dubliniensis. Conversely, deletion of CaNRG1 in C. albicans resulted in chlamydospore formation on Staib agar, confirming its central role in the regulation of this morphogenetic process. Our results demonstrate that differential regulation of a single gene, NRG1, in C. albicans and C. dubliniensis is responsible for their species‐specific response to environmental signals that induce chlamydospore development.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>15659176</pmid><doi>10.1111/j.1365-2958.2004.04414.x</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agar Biological and medical sciences Candida - genetics Candida - growth & development Candida - metabolism Candida - physiology Candida albicans - genetics Candida albicans - growth & development Candida albicans - metabolism Candida albicans - physiology Culture Media Fundamental and applied biological sciences. Psychology Gene expression Gene Expression Regulation, Fungal Genomics Humans Microbiology Miscellaneous Molecular biology Mycology Pathogens Repressor Proteins - genetics Repressor Proteins - metabolism Species Specificity Spores, Fungal - physiology Yeast |
title | Differential expression of the NRG1 repressor controls species‐specific regulation of chlamydospore development in Candida albicans and Candida dubliniensis |
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