The Satellite DNA PcH-Sat, Isolated and Characterized in the Limpet IPatella caerulea/I , Suggests the Origin from a Nin-SINE Transposable Element
Satellite DNA (sat-DNA) was previously described as junk and selfish DNA in the cellular economy, without a clear functional role. However, during the last two decades, evidence has been accumulated about the roles of sat-DNA in different cellular functions and its probable involvement in tumorigene...
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description | Satellite DNA (sat-DNA) was previously described as junk and selfish DNA in the cellular economy, without a clear functional role. However, during the last two decades, evidence has been accumulated about the roles of sat-DNA in different cellular functions and its probable involvement in tumorigenesis and adaptation to environmental changes. In molluscs, studies on sat-DNAs have been performed mainly on bivalve species, especially those of economic interest. Conversely, in Gastropoda (which includes about 80% of the currently described molluscs species), studies on sat-DNA have been largely neglected. In this study, we isolated and characterized a sat-DNA, here named PcH-sat, in the limpet Patella caerulea using the restriction enzyme method, particularly Hae III. Monomeric units of PcH-sat are 179 bp long, AT-rich (58.7%), and with an identity among monomers ranging from 91.6 to 99.8%. Southern blot showed that PcH-sat is conserved in P. depressa and P. ulyssiponensis , while a smeared signal of hybridization was present in the other three investigated limpets (P. ferruginea , P. rustica and P. vulgata ). Dot blot showed that PcH-sat represents about 10% of the genome of P. caerulea , 5% of that of P. depressa , and 0.3% of that of P. ulyssiponensis . FISH showed that PcH-sat was mainly localized on pericentromeric regions of chromosome pairs 2 and 4–7 of P. caerulea (2n = 18). A database search showed that PcH-sat contains a large segment (of 118 bp) showing high identity with a homologous trait of the Nin-SINE transposable element (TE) of the patellogastropod Lottia gigantea , supporting the hypothesis that TEs are involved in the rising and tandemization processes of sat-DNAs. |
doi_str_mv | 10.3390/genes15050541 |
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However, during the last two decades, evidence has been accumulated about the roles of sat-DNA in different cellular functions and its probable involvement in tumorigenesis and adaptation to environmental changes. In molluscs, studies on sat-DNAs have been performed mainly on bivalve species, especially those of economic interest. Conversely, in Gastropoda (which includes about 80% of the currently described molluscs species), studies on sat-DNA have been largely neglected. In this study, we isolated and characterized a sat-DNA, here named PcH-sat, in the limpet Patella caerulea using the restriction enzyme method, particularly Hae III. Monomeric units of PcH-sat are 179 bp long, AT-rich (58.7%), and with an identity among monomers ranging from 91.6 to 99.8%. Southern blot showed that PcH-sat is conserved in P. depressa and P. ulyssiponensis , while a smeared signal of hybridization was present in the other three investigated limpets (P. ferruginea , P. rustica and P. vulgata ). Dot blot showed that PcH-sat represents about 10% of the genome of P. caerulea , 5% of that of P. depressa , and 0.3% of that of P. ulyssiponensis . FISH showed that PcH-sat was mainly localized on pericentromeric regions of chromosome pairs 2 and 4–7 of P. caerulea (2n = 18). A database search showed that PcH-sat contains a large segment (of 118 bp) showing high identity with a homologous trait of the Nin-SINE transposable element (TE) of the patellogastropod Lottia gigantea , supporting the hypothesis that TEs are involved in the rising and tandemization processes of sat-DNAs.</description><identifier>ISSN: 2073-4425</identifier><identifier>EISSN: 2073-4425</identifier><identifier>DOI: 10.3390/genes15050541</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Origin ; Satellite DNA</subject><ispartof>Genes, 2024-05, Vol.15 (5)</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Petraccioli, Agnese</creatorcontrib><creatorcontrib>Maio, Nicola</creatorcontrib><creatorcontrib>Carotenuto, Rosa</creatorcontrib><creatorcontrib>Odierna, Gaetano</creatorcontrib><creatorcontrib>Guarino, Fabio Maria</creatorcontrib><title>The Satellite DNA PcH-Sat, Isolated and Characterized in the Limpet IPatella caerulea/I , Suggests the Origin from a Nin-SINE Transposable Element</title><title>Genes</title><description>Satellite DNA (sat-DNA) was previously described as junk and selfish DNA in the cellular economy, without a clear functional role. However, during the last two decades, evidence has been accumulated about the roles of sat-DNA in different cellular functions and its probable involvement in tumorigenesis and adaptation to environmental changes. In molluscs, studies on sat-DNAs have been performed mainly on bivalve species, especially those of economic interest. Conversely, in Gastropoda (which includes about 80% of the currently described molluscs species), studies on sat-DNA have been largely neglected. In this study, we isolated and characterized a sat-DNA, here named PcH-sat, in the limpet Patella caerulea using the restriction enzyme method, particularly Hae III. Monomeric units of PcH-sat are 179 bp long, AT-rich (58.7%), and with an identity among monomers ranging from 91.6 to 99.8%. Southern blot showed that PcH-sat is conserved in P. depressa and P. ulyssiponensis , while a smeared signal of hybridization was present in the other three investigated limpets (P. ferruginea , P. rustica and P. vulgata ). Dot blot showed that PcH-sat represents about 10% of the genome of P. caerulea , 5% of that of P. depressa , and 0.3% of that of P. ulyssiponensis . FISH showed that PcH-sat was mainly localized on pericentromeric regions of chromosome pairs 2 and 4–7 of P. caerulea (2n = 18). A database search showed that PcH-sat contains a large segment (of 118 bp) showing high identity with a homologous trait of the Nin-SINE transposable element (TE) of the patellogastropod Lottia gigantea , supporting the hypothesis that TEs are involved in the rising and tandemization processes of sat-DNAs.</description><subject>Origin</subject><subject>Satellite DNA</subject><issn>2073-4425</issn><issn>2073-4425</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptT7FuwjAUtKpWKqKM3S11JeAkTohHRGmJFAES2dFL8hxcOQ6KzdLP6BfXpR0Y-m54T_fuTjpCnkM2i2PB5i0atGHCPHh4R0YRW8QB51Fyf3M_kom1H8wPZxFjyYh8lSekB3CotXJIX7dLuq83gWemNLe99p-Ggmno6gQD1A4H9ekZZajzxkJ1Z3Q0318DgNaAw0UjzHM6pYdL26J19qrcDar1Jjn0HQW6VSY45Ns1LQcw9txbqDTStcYOjXsiDxK0xcnfHpPybV2uNkGxe89XyyJoU18nYXGITHDfNk1R8kqysA5lxStfTGZSpFkDWcQTSLMk5CBQ1GkFVSwiJhYRxmPy8hvbgsajMrJ3vmCnbH1cLkTyo-OxV83-UXk02Km6NyiV528M3-jNdcg</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Petraccioli, Agnese</creator><creator>Maio, Nicola</creator><creator>Carotenuto, Rosa</creator><creator>Odierna, Gaetano</creator><creator>Guarino, Fabio Maria</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20240501</creationdate><title>The Satellite DNA PcH-Sat, Isolated and Characterized in the Limpet IPatella caerulea/I , Suggests the Origin from a Nin-SINE Transposable Element</title><author>Petraccioli, Agnese ; Maio, Nicola ; Carotenuto, Rosa ; Odierna, Gaetano ; Guarino, Fabio Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g673-5031e09454166ef4bf01c1fb4b200f8f968da8245a68514a9e9c6bab3920972e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Origin</topic><topic>Satellite DNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petraccioli, Agnese</creatorcontrib><creatorcontrib>Maio, Nicola</creatorcontrib><creatorcontrib>Carotenuto, Rosa</creatorcontrib><creatorcontrib>Odierna, Gaetano</creatorcontrib><creatorcontrib>Guarino, Fabio Maria</creatorcontrib><jtitle>Genes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petraccioli, Agnese</au><au>Maio, Nicola</au><au>Carotenuto, Rosa</au><au>Odierna, Gaetano</au><au>Guarino, Fabio Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Satellite DNA PcH-Sat, Isolated and Characterized in the Limpet IPatella caerulea/I , Suggests the Origin from a Nin-SINE Transposable Element</atitle><jtitle>Genes</jtitle><date>2024-05-01</date><risdate>2024</risdate><volume>15</volume><issue>5</issue><issn>2073-4425</issn><eissn>2073-4425</eissn><abstract>Satellite DNA (sat-DNA) was previously described as junk and selfish DNA in the cellular economy, without a clear functional role. However, during the last two decades, evidence has been accumulated about the roles of sat-DNA in different cellular functions and its probable involvement in tumorigenesis and adaptation to environmental changes. In molluscs, studies on sat-DNAs have been performed mainly on bivalve species, especially those of economic interest. Conversely, in Gastropoda (which includes about 80% of the currently described molluscs species), studies on sat-DNA have been largely neglected. In this study, we isolated and characterized a sat-DNA, here named PcH-sat, in the limpet Patella caerulea using the restriction enzyme method, particularly Hae III. Monomeric units of PcH-sat are 179 bp long, AT-rich (58.7%), and with an identity among monomers ranging from 91.6 to 99.8%. Southern blot showed that PcH-sat is conserved in P. depressa and P. ulyssiponensis , while a smeared signal of hybridization was present in the other three investigated limpets (P. ferruginea , P. rustica and P. vulgata ). Dot blot showed that PcH-sat represents about 10% of the genome of P. caerulea , 5% of that of P. depressa , and 0.3% of that of P. ulyssiponensis . FISH showed that PcH-sat was mainly localized on pericentromeric regions of chromosome pairs 2 and 4–7 of P. caerulea (2n = 18). A database search showed that PcH-sat contains a large segment (of 118 bp) showing high identity with a homologous trait of the Nin-SINE transposable element (TE) of the patellogastropod Lottia gigantea , supporting the hypothesis that TEs are involved in the rising and tandemization processes of sat-DNAs.</abstract><pub>MDPI AG</pub><doi>10.3390/genes15050541</doi></addata></record> |
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title | The Satellite DNA PcH-Sat, Isolated and Characterized in the Limpet IPatella caerulea/I , Suggests the Origin from a Nin-SINE Transposable Element |
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