Breeding systems in the lichen-forming fungal genus Cladonia
The breeding systems of three species of the lichen-forming fungal genus Cladonia were investigated. Cladonia floerkeana, Cladonia galindezii, and Cladonia portentosa were selected due to their contrasting ecologies and reproductive strategies, and because they belong to the Lecanorales, the major l...
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Veröffentlicht in: | Fungal genetics and biology 2005-06, Vol.42 (6), p.554-563 |
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creator | Seymour, Fabian A. Crittenden, Peter D. Dickinson, Matthew J. Paoletti, Mathieu Montiel, Dolores Cho, Lily Dyer, Paul S. |
description | The breeding systems of three species of the lichen-forming fungal genus
Cladonia were investigated.
Cladonia floerkeana,
Cladonia galindezii, and
Cladonia portentosa were selected due to their contrasting ecologies and reproductive strategies, and because they belong to the Lecanorales, the major lichen-forming order. Sibling single-spore progeny were collected from apothecia and used to establish axenic cultures. Two experimental approaches were used to determine breeding systems. First, RAPD-PCR and AFLP fingerprinting revealed that spores from the same apothecium were not genetically uniform, indicating heterothallism in each of these species. Second, segregation of a
MAT-2 mating-type gene was assessed using degenerate PCR primers designed to amplify the high-mobility group region. A
MAT-2 gene occurred in 40–60% of progeny, consistent with a heterothallic breeding system. The PCR product from
C. galindezii was cloned and sequenced, and confirmed to have the characteristic motifs of a
MAT-2 HMG gene. This is thought to be the first report of the use of segregation of a mating-type gene among ascospore progeny to determine the breeding system of a fungal species. The ecological significance of the results is discussed. |
doi_str_mv | 10.1016/j.fgb.2005.03.006 |
format | Article |
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Cladonia were investigated.
Cladonia floerkeana,
Cladonia galindezii, and
Cladonia portentosa were selected due to their contrasting ecologies and reproductive strategies, and because they belong to the Lecanorales, the major lichen-forming order. Sibling single-spore progeny were collected from apothecia and used to establish axenic cultures. Two experimental approaches were used to determine breeding systems. First, RAPD-PCR and AFLP fingerprinting revealed that spores from the same apothecium were not genetically uniform, indicating heterothallism in each of these species. Second, segregation of a
MAT-2 mating-type gene was assessed using degenerate PCR primers designed to amplify the high-mobility group region. A
MAT-2 gene occurred in 40–60% of progeny, consistent with a heterothallic breeding system. The PCR product from
C. galindezii was cloned and sequenced, and confirmed to have the characteristic motifs of a
MAT-2 HMG gene. This is thought to be the first report of the use of segregation of a mating-type gene among ascospore progeny to determine the breeding system of a fungal species. The ecological significance of the results is discussed.</description><identifier>ISSN: 1087-1845</identifier><identifier>EISSN: 1096-0937</identifier><identifier>DOI: 10.1016/j.fgb.2005.03.006</identifier><identifier>PMID: 15893256</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>AFLP ; Amino Acid Sequence ; amplified fragment length polymorphism ; Ascomycota - genetics ; Ascomycota - physiology ; Breeding system ; Cladonia ; Cladonia floerkeana ; Cladonia galindezii ; Cladonia portentosa ; Cluster Analysis ; DNA Fingerprinting ; DNA, Fungal - analysis ; DNA, Fungal - chemistry ; DNA, Fungal - genetics ; gene segregation ; genes ; Genes, Fungal ; Genes, Mating Type, Fungal ; Heterothallism ; High Mobility Group Proteins - genetics ; Lecanorales ; Lichen-forming fungus ; Lichens - physiology ; MAT-2 gene ; Mating type ; mating types ; Molecular Sequence Data ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Random Amplified Polymorphic DNA Technique ; RAPD ; Sequence Alignment ; Sequence Analysis, DNA ; Sequence Homology ; sexual reproduction ; Spores, Fungal - genetics ; Spores, Fungal - physiology</subject><ispartof>Fungal genetics and biology, 2005-06, Vol.42 (6), p.554-563</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-2c482114b7e165dddcf2e3e506cbd0381dd9899c970315657d08aae3fc39ca53</citedby><cites>FETCH-LOGICAL-c437t-2c482114b7e165dddcf2e3e506cbd0381dd9899c970315657d08aae3fc39ca53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1087184505000496$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15893256$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seymour, Fabian A.</creatorcontrib><creatorcontrib>Crittenden, Peter D.</creatorcontrib><creatorcontrib>Dickinson, Matthew J.</creatorcontrib><creatorcontrib>Paoletti, Mathieu</creatorcontrib><creatorcontrib>Montiel, Dolores</creatorcontrib><creatorcontrib>Cho, Lily</creatorcontrib><creatorcontrib>Dyer, Paul S.</creatorcontrib><title>Breeding systems in the lichen-forming fungal genus Cladonia</title><title>Fungal genetics and biology</title><addtitle>Fungal Genet Biol</addtitle><description>The breeding systems of three species of the lichen-forming fungal genus
Cladonia were investigated.
Cladonia floerkeana,
Cladonia galindezii, and
Cladonia portentosa were selected due to their contrasting ecologies and reproductive strategies, and because they belong to the Lecanorales, the major lichen-forming order. Sibling single-spore progeny were collected from apothecia and used to establish axenic cultures. Two experimental approaches were used to determine breeding systems. First, RAPD-PCR and AFLP fingerprinting revealed that spores from the same apothecium were not genetically uniform, indicating heterothallism in each of these species. Second, segregation of a
MAT-2 mating-type gene was assessed using degenerate PCR primers designed to amplify the high-mobility group region. A
MAT-2 gene occurred in 40–60% of progeny, consistent with a heterothallic breeding system. The PCR product from
C. galindezii was cloned and sequenced, and confirmed to have the characteristic motifs of a
MAT-2 HMG gene. This is thought to be the first report of the use of segregation of a mating-type gene among ascospore progeny to determine the breeding system of a fungal species. The ecological significance of the results is discussed.</description><subject>AFLP</subject><subject>Amino Acid Sequence</subject><subject>amplified fragment length polymorphism</subject><subject>Ascomycota - genetics</subject><subject>Ascomycota - physiology</subject><subject>Breeding system</subject><subject>Cladonia</subject><subject>Cladonia floerkeana</subject><subject>Cladonia galindezii</subject><subject>Cladonia portentosa</subject><subject>Cluster Analysis</subject><subject>DNA Fingerprinting</subject><subject>DNA, Fungal - analysis</subject><subject>DNA, Fungal - chemistry</subject><subject>DNA, Fungal - genetics</subject><subject>gene segregation</subject><subject>genes</subject><subject>Genes, Fungal</subject><subject>Genes, Mating Type, Fungal</subject><subject>Heterothallism</subject><subject>High Mobility Group Proteins - genetics</subject><subject>Lecanorales</subject><subject>Lichen-forming fungus</subject><subject>Lichens - physiology</subject><subject>MAT-2 gene</subject><subject>Mating type</subject><subject>mating types</subject><subject>Molecular Sequence Data</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Genetic</subject><subject>Random Amplified Polymorphic DNA Technique</subject><subject>RAPD</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, DNA</subject><subject>Sequence Homology</subject><subject>sexual reproduction</subject><subject>Spores, Fungal - genetics</subject><subject>Spores, Fungal - physiology</subject><issn>1087-1845</issn><issn>1096-0937</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EoqXwA7hATtwSZuz4I4JLWfElVeJAOVtee5J6lY9iJ0j993i1K3GjJ4_k5301moex1wgNAqr3h6Yf9g0HkA2IBkA9YZcInaqhE_rpcTa6RtPKC_Yi5wMAomzxObtAaTrBpbpkHz8lohDnocoPeaUpV3Gu1juqxujvaK77JU3H336bBzdWA81brnajC8sc3Uv2rHdjplfn94rdfvl8u_tW3_z4-n13fVP7Vui15r41HLHda0IlQwi-5yRIgvL7AMJgCJ3pOt9pECiV1AGMcyR6LzrvpLhi706192n5vVFe7RSzp3F0My1btkobUWL4KMjBoOb8cRC1hBaFKiCeQJ-WnBP19j7FyaUHi2CPDuzBFgf26MCCsMVBybw5l2_7icK_xPnoBXh7Anq3WDekmO2vnxxQQGmEDtpCfDgRVK76J1Ky2UeafTGVyK82LPE_C_wF3k2eoA</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Seymour, Fabian A.</creator><creator>Crittenden, Peter D.</creator><creator>Dickinson, Matthew J.</creator><creator>Paoletti, Mathieu</creator><creator>Montiel, Dolores</creator><creator>Cho, Lily</creator><creator>Dyer, Paul S.</creator><general>Elsevier Inc</general><scope>FBQ</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>20050601</creationdate><title>Breeding systems in the lichen-forming fungal genus Cladonia</title><author>Seymour, Fabian A. ; Crittenden, Peter D. ; Dickinson, Matthew J. ; Paoletti, Mathieu ; Montiel, Dolores ; Cho, Lily ; Dyer, Paul S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-2c482114b7e165dddcf2e3e506cbd0381dd9899c970315657d08aae3fc39ca53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>AFLP</topic><topic>Amino Acid Sequence</topic><topic>amplified fragment length polymorphism</topic><topic>Ascomycota - genetics</topic><topic>Ascomycota - physiology</topic><topic>Breeding system</topic><topic>Cladonia</topic><topic>Cladonia floerkeana</topic><topic>Cladonia galindezii</topic><topic>Cladonia portentosa</topic><topic>Cluster Analysis</topic><topic>DNA Fingerprinting</topic><topic>DNA, Fungal - analysis</topic><topic>DNA, Fungal - chemistry</topic><topic>DNA, Fungal - genetics</topic><topic>gene segregation</topic><topic>genes</topic><topic>Genes, Fungal</topic><topic>Genes, Mating Type, Fungal</topic><topic>Heterothallism</topic><topic>High Mobility Group Proteins - genetics</topic><topic>Lecanorales</topic><topic>Lichen-forming fungus</topic><topic>Lichens - physiology</topic><topic>MAT-2 gene</topic><topic>Mating type</topic><topic>mating types</topic><topic>Molecular Sequence Data</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Genetic</topic><topic>Random Amplified Polymorphic DNA Technique</topic><topic>RAPD</topic><topic>Sequence Alignment</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology</topic><topic>sexual reproduction</topic><topic>Spores, Fungal - genetics</topic><topic>Spores, Fungal - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seymour, Fabian A.</creatorcontrib><creatorcontrib>Crittenden, Peter D.</creatorcontrib><creatorcontrib>Dickinson, Matthew J.</creatorcontrib><creatorcontrib>Paoletti, Mathieu</creatorcontrib><creatorcontrib>Montiel, Dolores</creatorcontrib><creatorcontrib>Cho, Lily</creatorcontrib><creatorcontrib>Dyer, Paul S.</creatorcontrib><collection>AGRIS</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>Fungal genetics and biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seymour, Fabian A.</au><au>Crittenden, Peter D.</au><au>Dickinson, Matthew J.</au><au>Paoletti, Mathieu</au><au>Montiel, Dolores</au><au>Cho, Lily</au><au>Dyer, Paul S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Breeding systems in the lichen-forming fungal genus Cladonia</atitle><jtitle>Fungal genetics and biology</jtitle><addtitle>Fungal Genet Biol</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>42</volume><issue>6</issue><spage>554</spage><epage>563</epage><pages>554-563</pages><issn>1087-1845</issn><eissn>1096-0937</eissn><abstract>The breeding systems of three species of the lichen-forming fungal genus
Cladonia were investigated.
Cladonia floerkeana,
Cladonia galindezii, and
Cladonia portentosa were selected due to their contrasting ecologies and reproductive strategies, and because they belong to the Lecanorales, the major lichen-forming order. Sibling single-spore progeny were collected from apothecia and used to establish axenic cultures. Two experimental approaches were used to determine breeding systems. First, RAPD-PCR and AFLP fingerprinting revealed that spores from the same apothecium were not genetically uniform, indicating heterothallism in each of these species. Second, segregation of a
MAT-2 mating-type gene was assessed using degenerate PCR primers designed to amplify the high-mobility group region. A
MAT-2 gene occurred in 40–60% of progeny, consistent with a heterothallic breeding system. The PCR product from
C. galindezii was cloned and sequenced, and confirmed to have the characteristic motifs of a
MAT-2 HMG gene. This is thought to be the first report of the use of segregation of a mating-type gene among ascospore progeny to determine the breeding system of a fungal species. The ecological significance of the results is discussed.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15893256</pmid><doi>10.1016/j.fgb.2005.03.006</doi><tpages>10</tpages></addata></record> |
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subjects | AFLP Amino Acid Sequence amplified fragment length polymorphism Ascomycota - genetics Ascomycota - physiology Breeding system Cladonia Cladonia floerkeana Cladonia galindezii Cladonia portentosa Cluster Analysis DNA Fingerprinting DNA, Fungal - analysis DNA, Fungal - chemistry DNA, Fungal - genetics gene segregation genes Genes, Fungal Genes, Mating Type, Fungal Heterothallism High Mobility Group Proteins - genetics Lecanorales Lichen-forming fungus Lichens - physiology MAT-2 gene Mating type mating types Molecular Sequence Data Polymerase Chain Reaction Polymorphism, Genetic Random Amplified Polymorphic DNA Technique RAPD Sequence Alignment Sequence Analysis, DNA Sequence Homology sexual reproduction Spores, Fungal - genetics Spores, Fungal - physiology |
title | Breeding systems in the lichen-forming fungal genus Cladonia |
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