Genes within Genes: Multiple LAGLIDADG Homing Endonucleases Target the Ribosomal Protein S3 Gene Encoded within an rnl Group I Intron of Ophiostoma and Related Taxa
In some ascomycete fungi, ribosomal protein S3 (Rps3) is encoded within a group I intron (mL2449) that is inserted in the U11 region of the mitochondrial large subunit rDNA (rnl) gene. Previous characterization of the mL2449 intron in strains of Ophiostoma novo-ulmi subspecies americana (Dutch Elm D...
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description | In some ascomycete fungi, ribosomal protein S3 (Rps3) is encoded within a group I intron (mL2449) that is inserted in the U11 region of the mitochondrial large subunit rDNA (rnl) gene. Previous characterization of the mL2449 intron in strains of Ophiostoma novo-ulmi subspecies americana (Dutch Elm Disease) revealed a complex genes-within-genes arrangement whereby a LAGLIDADG homing endonuclease gene (HEG) is inserted into the RPS3 gene near the 3′ terminus, creating a hybrid Rps3-LAGLIDADG fusion protein. Here, we examined 119 additional strains of Ophiostoma and related taxa representing 85 different species by a polymerase chain reaction- based survey and detected both short (∼1.6 kb) and long (>2.2 kb) versions of the mL2449 intron in 88 and 31 strains, respectively. Among the long versions encountered, 21 were sequenced, revealing the presence of either intact or degenerated HEG-coding regions inserted within the RPS3 gene. Surprisingly, we identified two new HEG insertion sites in RPS3; one near the original C-terminal insertion site and one near the N-terminus of RPS3. In all instances, the HEGs are fused in-frame with the RPS3-coding sequences to create fusion proteins. However, comparative sequence analysis showed that upon insertion, the HEGs displaced a portion of the RPS3-coding region. Remarkably, the displaced RPS3-coding segments are duplicated and fused in-frame to the 3′ end of RPS3, restoring a full-length RPS3 gene. We cloned and expressed the LAGLIDADG portion of two Rps3-HEG fusions, and showed that I-OnuI and I-LtrI generate 4 nucleotide (nt), 3′ overhangs, and cleave at or 1 nt upstream of the HEG insertion site, respectively. Collectively, our data indicate that RPS3 genes are a refuge for distinct types of LAGLIDADG HEGs that are defined by the presence of duplicated segments of the host gene that restore the RPS3 gene, thus minimizing the impact of the HEG insertion on Rps3 function. |
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C. ; Edgell, D. R. ; Hausner, G.</creator><creatorcontrib>Sethuraman, J. ; Majer, A. ; Friedrich, N. C. ; Edgell, D. R. ; Hausner, G.</creatorcontrib><description>In some ascomycete fungi, ribosomal protein S3 (Rps3) is encoded within a group I intron (mL2449) that is inserted in the U11 region of the mitochondrial large subunit rDNA (rnl) gene. Previous characterization of the mL2449 intron in strains of Ophiostoma novo-ulmi subspecies americana (Dutch Elm Disease) revealed a complex genes-within-genes arrangement whereby a LAGLIDADG homing endonuclease gene (HEG) is inserted into the RPS3 gene near the 3′ terminus, creating a hybrid Rps3-LAGLIDADG fusion protein. Here, we examined 119 additional strains of Ophiostoma and related taxa representing 85 different species by a polymerase chain reaction- based survey and detected both short (∼1.6 kb) and long (>2.2 kb) versions of the mL2449 intron in 88 and 31 strains, respectively. Among the long versions encountered, 21 were sequenced, revealing the presence of either intact or degenerated HEG-coding regions inserted within the RPS3 gene. Surprisingly, we identified two new HEG insertion sites in RPS3; one near the original C-terminal insertion site and one near the N-terminus of RPS3. In all instances, the HEGs are fused in-frame with the RPS3-coding sequences to create fusion proteins. However, comparative sequence analysis showed that upon insertion, the HEGs displaced a portion of the RPS3-coding region. Remarkably, the displaced RPS3-coding segments are duplicated and fused in-frame to the 3′ end of RPS3, restoring a full-length RPS3 gene. We cloned and expressed the LAGLIDADG portion of two Rps3-HEG fusions, and showed that I-OnuI and I-LtrI generate 4 nucleotide (nt), 3′ overhangs, and cleave at or 1 nt upstream of the HEG insertion site, respectively. Collectively, our data indicate that RPS3 genes are a refuge for distinct types of LAGLIDADG HEGs that are defined by the presence of duplicated segments of the host gene that restore the RPS3 gene, thus minimizing the impact of the HEG insertion on Rps3 function.</description><identifier>ISSN: 0737-4038</identifier><identifier>EISSN: 1537-1719</identifier><identifier>DOI: 10.1093/molbev/msp145</identifier><identifier>PMID: 19597163</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Amino Acid Motifs ; Amino Acid Sequence ; Ascomycetes ; Base Sequence ; Data processing ; Dutch elm disease ; Endonucleases - chemistry ; Endonucleases - genetics ; Endonucleases - isolation & purification ; Fungal Proteins - chemistry ; Fungal Proteins - genetics ; Fungal Proteins - isolation & purification ; Fungi ; Fusion protein ; Genes, Fungal ; homing endonuclease ; Hybrids ; Inheritance Patterns - genetics ; Introns ; Introns - genetics ; Mitochondria ; Mitochondrial DNA ; Molecular biology ; Molecular Sequence Data ; Mutagenesis, Insertional ; N-Terminus ; Nucleotides ; Open Reading Frames - genetics ; Ophiostoma ; Ophiostoma - classification ; Ophiostoma - enzymology ; Ophiostoma - genetics ; Ophiostoma novo-ulmi ; Phylogeny ; Plant pathology ; Polymerase Chain Reaction ; Proteins ; ribosomal protein S3 ; Ribosomal Proteins - genetics ; Ribosome Subunits, Large - genetics ; rps3 gene ; Taxa</subject><ispartof>Molecular biology and evolution, 2009-10, Vol.26 (10), p.2299-2315</ispartof><rights>The Author 2009. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org 2009</rights><rights>The Author 2009. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-5ea5d0051b805751447ad40481a08b09803314dde035cb012a5558cc382b29b13</citedby><cites>FETCH-LOGICAL-c421t-5ea5d0051b805751447ad40481a08b09803314dde035cb012a5558cc382b29b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1598,27903,27904</link.rule.ids><linktorsrc>$$Uhttps://dx.doi.org/10.1093/molbev/msp145$$EView_record_in_Oxford_University_Press$$FView_record_in_$$GOxford_University_Press</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19597163$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sethuraman, J.</creatorcontrib><creatorcontrib>Majer, A.</creatorcontrib><creatorcontrib>Friedrich, N. C.</creatorcontrib><creatorcontrib>Edgell, D. R.</creatorcontrib><creatorcontrib>Hausner, G.</creatorcontrib><title>Genes within Genes: Multiple LAGLIDADG Homing Endonucleases Target the Ribosomal Protein S3 Gene Encoded within an rnl Group I Intron of Ophiostoma and Related Taxa</title><title>Molecular biology and evolution</title><addtitle>Mol Biol Evol</addtitle><description>In some ascomycete fungi, ribosomal protein S3 (Rps3) is encoded within a group I intron (mL2449) that is inserted in the U11 region of the mitochondrial large subunit rDNA (rnl) gene. Previous characterization of the mL2449 intron in strains of Ophiostoma novo-ulmi subspecies americana (Dutch Elm Disease) revealed a complex genes-within-genes arrangement whereby a LAGLIDADG homing endonuclease gene (HEG) is inserted into the RPS3 gene near the 3′ terminus, creating a hybrid Rps3-LAGLIDADG fusion protein. Here, we examined 119 additional strains of Ophiostoma and related taxa representing 85 different species by a polymerase chain reaction- based survey and detected both short (∼1.6 kb) and long (>2.2 kb) versions of the mL2449 intron in 88 and 31 strains, respectively. Among the long versions encountered, 21 were sequenced, revealing the presence of either intact or degenerated HEG-coding regions inserted within the RPS3 gene. Surprisingly, we identified two new HEG insertion sites in RPS3; one near the original C-terminal insertion site and one near the N-terminus of RPS3. In all instances, the HEGs are fused in-frame with the RPS3-coding sequences to create fusion proteins. However, comparative sequence analysis showed that upon insertion, the HEGs displaced a portion of the RPS3-coding region. Remarkably, the displaced RPS3-coding segments are duplicated and fused in-frame to the 3′ end of RPS3, restoring a full-length RPS3 gene. We cloned and expressed the LAGLIDADG portion of two Rps3-HEG fusions, and showed that I-OnuI and I-LtrI generate 4 nucleotide (nt), 3′ overhangs, and cleave at or 1 nt upstream of the HEG insertion site, respectively. Collectively, our data indicate that RPS3 genes are a refuge for distinct types of LAGLIDADG HEGs that are defined by the presence of duplicated segments of the host gene that restore the RPS3 gene, thus minimizing the impact of the HEG insertion on Rps3 function.</description><subject>Amino Acid Motifs</subject><subject>Amino Acid Sequence</subject><subject>Ascomycetes</subject><subject>Base Sequence</subject><subject>Data processing</subject><subject>Dutch elm disease</subject><subject>Endonucleases - chemistry</subject><subject>Endonucleases - genetics</subject><subject>Endonucleases - isolation & purification</subject><subject>Fungal Proteins - chemistry</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - isolation & purification</subject><subject>Fungi</subject><subject>Fusion protein</subject><subject>Genes, Fungal</subject><subject>homing endonuclease</subject><subject>Hybrids</subject><subject>Inheritance Patterns - genetics</subject><subject>Introns</subject><subject>Introns - genetics</subject><subject>Mitochondria</subject><subject>Mitochondrial DNA</subject><subject>Molecular biology</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis, Insertional</subject><subject>N-Terminus</subject><subject>Nucleotides</subject><subject>Open Reading Frames - genetics</subject><subject>Ophiostoma</subject><subject>Ophiostoma - classification</subject><subject>Ophiostoma - enzymology</subject><subject>Ophiostoma - genetics</subject><subject>Ophiostoma novo-ulmi</subject><subject>Phylogeny</subject><subject>Plant pathology</subject><subject>Polymerase Chain Reaction</subject><subject>Proteins</subject><subject>ribosomal protein S3</subject><subject>Ribosomal Proteins - genetics</subject><subject>Ribosome Subunits, Large - genetics</subject><subject>rps3 gene</subject><subject>Taxa</subject><issn>0737-4038</issn><issn>1537-1719</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkc1u1DAURi0EokNhyRZZLBCbtNexPUnYjdqSjjRVURnWkRPf6aRy7NR2-HkfHhS3GYTEpivb0vmOr_0R8pbBCYOKnw7OtPj9dAgjE_IZWTDJi4wVrHpOFlCkvQBeHpFXIdwBMCGWy5fkiFWyKtiSL8jvGi0G-qOP-97Sx8MnejWZ2I8G6WZVb9bnq_OaXrqht7f0wmpnp86gCim1Vf4WI417pDd964IblKFfvIuYXF_5oy5FOqdR_71CWeqtobV300jXdG2jd5a6Hb0e970LMTkSo-kNGhVTbKt-qtfkxU6ZgG8O6zH59vlie3aZba7r9dlqk3UiZzGTqKQGkKwtQRYyPbZQWoAomYKyhaoEzpnQGoHLrgWWKyll2XW8zNu8ahk_Jh9m7-jd_YQhNkMfOjRGWXRTaHIGRQ6iSuD7_8A7N3mbZmtynpeCF7JMUDZDnXcheNw1o-8H5X81DJqH7pq5u2buLvHvDtKpHVD_ow9lJeDjDKSve8L1B8JMo9Y</recordid><startdate>200910</startdate><enddate>200910</enddate><creator>Sethuraman, J.</creator><creator>Majer, A.</creator><creator>Friedrich, N. 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C.</au><au>Edgell, D. R.</au><au>Hausner, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genes within Genes: Multiple LAGLIDADG Homing Endonucleases Target the Ribosomal Protein S3 Gene Encoded within an rnl Group I Intron of Ophiostoma and Related Taxa</atitle><jtitle>Molecular biology and evolution</jtitle><addtitle>Mol Biol Evol</addtitle><date>2009-10</date><risdate>2009</risdate><volume>26</volume><issue>10</issue><spage>2299</spage><epage>2315</epage><pages>2299-2315</pages><issn>0737-4038</issn><eissn>1537-1719</eissn><abstract>In some ascomycete fungi, ribosomal protein S3 (Rps3) is encoded within a group I intron (mL2449) that is inserted in the U11 region of the mitochondrial large subunit rDNA (rnl) gene. Previous characterization of the mL2449 intron in strains of Ophiostoma novo-ulmi subspecies americana (Dutch Elm Disease) revealed a complex genes-within-genes arrangement whereby a LAGLIDADG homing endonuclease gene (HEG) is inserted into the RPS3 gene near the 3′ terminus, creating a hybrid Rps3-LAGLIDADG fusion protein. Here, we examined 119 additional strains of Ophiostoma and related taxa representing 85 different species by a polymerase chain reaction- based survey and detected both short (∼1.6 kb) and long (>2.2 kb) versions of the mL2449 intron in 88 and 31 strains, respectively. Among the long versions encountered, 21 were sequenced, revealing the presence of either intact or degenerated HEG-coding regions inserted within the RPS3 gene. Surprisingly, we identified two new HEG insertion sites in RPS3; one near the original C-terminal insertion site and one near the N-terminus of RPS3. In all instances, the HEGs are fused in-frame with the RPS3-coding sequences to create fusion proteins. However, comparative sequence analysis showed that upon insertion, the HEGs displaced a portion of the RPS3-coding region. Remarkably, the displaced RPS3-coding segments are duplicated and fused in-frame to the 3′ end of RPS3, restoring a full-length RPS3 gene. We cloned and expressed the LAGLIDADG portion of two Rps3-HEG fusions, and showed that I-OnuI and I-LtrI generate 4 nucleotide (nt), 3′ overhangs, and cleave at or 1 nt upstream of the HEG insertion site, respectively. Collectively, our data indicate that RPS3 genes are a refuge for distinct types of LAGLIDADG HEGs that are defined by the presence of duplicated segments of the host gene that restore the RPS3 gene, thus minimizing the impact of the HEG insertion on Rps3 function.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>19597163</pmid><doi>10.1093/molbev/msp145</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Motifs Amino Acid Sequence Ascomycetes Base Sequence Data processing Dutch elm disease Endonucleases - chemistry Endonucleases - genetics Endonucleases - isolation & purification Fungal Proteins - chemistry Fungal Proteins - genetics Fungal Proteins - isolation & purification Fungi Fusion protein Genes, Fungal homing endonuclease Hybrids Inheritance Patterns - genetics Introns Introns - genetics Mitochondria Mitochondrial DNA Molecular biology Molecular Sequence Data Mutagenesis, Insertional N-Terminus Nucleotides Open Reading Frames - genetics Ophiostoma Ophiostoma - classification Ophiostoma - enzymology Ophiostoma - genetics Ophiostoma novo-ulmi Phylogeny Plant pathology Polymerase Chain Reaction Proteins ribosomal protein S3 Ribosomal Proteins - genetics Ribosome Subunits, Large - genetics rps3 gene Taxa |
title | Genes within Genes: Multiple LAGLIDADG Homing Endonucleases Target the Ribosomal Protein S3 Gene Encoded within an rnl Group I Intron of Ophiostoma and Related Taxa |
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