Characterization of the DNA nucleotide sequences in the genome of red sea bream iridoviruses isolated in Korea
The nucleotide sequences of DNA fragments amplified by polymerase chain reaction (PCR) from four different genomic regions of nine red sea bream iridoviruses (RSIVs) isolated from different species of fish, different areas and in different years in Korea were compared with the reported reference seq...
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description | The nucleotide sequences of DNA fragments amplified by polymerase chain reaction (PCR) from four different genomic regions of nine red sea bream iridoviruses (RSIVs) isolated from different species of fish, different areas and in different years in Korea were compared with the reported reference sequences. One isolate, RSIV Namhae, showed 100% homology to the reference sequences, while the other eight isolates, which appeared to contain identical nucleotide sequences, showed 96.6–98.9% homology with reference sequences depending upon the target regions of PCR gene amplification. However, differences in nucleotide sequences were not apparent between the RSIVs isolated in different locations, in different years or in different host species. We also cloned and sequenced the 3′ end flanking region (K1) of the DNA polymerase (DPOL) gene using the cassette ligation-mediated PCR method. This sequence was 4436-bp long and possessed two open reading frames (ORF-1 and ORF-2) oriented in opposite directions. The putative proteins encoded by these two ORFs could not be characterized by comparison with the proteins of other species in the data banks. The presence of the ribonucleotide reductase small subunit (RNRS) gene at the 3′ end of the K1 region allowed us to determine that these two genes, RNRS and DPOL, are separated 5508 bp and oriented in the same direction in the genome of RSIV. Moreover, it is of interest that a
PstI-restriction fragment, of which the sequence but not the location within the RSIV genome had previously been reported, is located at nucleotide positions from 1096 to 2054, extending from within the ORF-1 region, spanning the intervening sequence between ORF-1 and ORF-2, and extending into the ORF-2 region. Various repeating sequences up to 86 bp were present at the 3′ ends of ORFs, especially within the nucleotide sequences at the 3′ terminus of ORF-2. No similarities were detected when the DNA sequences of the K1 region were compared to the DNA sequences of a repetitive element in the genome of other iridoviruses. |
doi_str_mv | 10.1016/S0044-8486(02)00538-0 |
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PstI-restriction fragment, of which the sequence but not the location within the RSIV genome had previously been reported, is located at nucleotide positions from 1096 to 2054, extending from within the ORF-1 region, spanning the intervening sequence between ORF-1 and ORF-2, and extending into the ORF-2 region. Various repeating sequences up to 86 bp were present at the 3′ ends of ORFs, especially within the nucleotide sequences at the 3′ terminus of ORF-2. No similarities were detected when the DNA sequences of the K1 region were compared to the DNA sequences of a repetitive element in the genome of other iridoviruses.</description><identifier>ISSN: 0044-8486</identifier><identifier>EISSN: 1873-5622</identifier><identifier>DOI: 10.1016/S0044-8486(02)00538-0</identifier><identifier>CODEN: AQCLAL</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animal aquaculture ; Animal productions ; Aquaculture ; Biological and medical sciences ; Cassette ligation-mediated PCR ; Chrysophrys major ; Deoxyribonucleic acid ; DNA ; DNA homology ; Fish ; Fundamental and applied biological sciences. Psychology ; Gene amplification ; Genetics ; Iridovirus ; Marine ; Microbiology ; Pisciculture ; Red sea bream ; Repetitive element ; Vertebrate aquaculture ; Virology</subject><ispartof>Aquaculture, 2003-04, Vol.220 (1), p.119-133</ispartof><rights>2003 Elsevier Science B.V.</rights><rights>2003 INIST-CNRS</rights><rights>Copyright Elsevier Sequoia S.A. Apr 14, 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-bd6ffa60aaa3385048aa54373eee4c217cc271e7f01a4dc2274621ca6ac22f603</citedby><cites>FETCH-LOGICAL-c395t-bd6ffa60aaa3385048aa54373eee4c217cc271e7f01a4dc2274621ca6ac22f603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0044-8486(02)00538-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14637672$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeong, Joon Bum</creatorcontrib><creatorcontrib>Jun, Lyu Jin</creatorcontrib><creatorcontrib>Yoo, Min Ho</creatorcontrib><creatorcontrib>Kim, Myong Sug</creatorcontrib><creatorcontrib>Komisar, Jack L</creatorcontrib><creatorcontrib>Jeong, Hyun Do</creatorcontrib><title>Characterization of the DNA nucleotide sequences in the genome of red sea bream iridoviruses isolated in Korea</title><title>Aquaculture</title><description>The nucleotide sequences of DNA fragments amplified by polymerase chain reaction (PCR) from four different genomic regions of nine red sea bream iridoviruses (RSIVs) isolated from different species of fish, different areas and in different years in Korea were compared with the reported reference sequences. One isolate, RSIV Namhae, showed 100% homology to the reference sequences, while the other eight isolates, which appeared to contain identical nucleotide sequences, showed 96.6–98.9% homology with reference sequences depending upon the target regions of PCR gene amplification. However, differences in nucleotide sequences were not apparent between the RSIVs isolated in different locations, in different years or in different host species. We also cloned and sequenced the 3′ end flanking region (K1) of the DNA polymerase (DPOL) gene using the cassette ligation-mediated PCR method. This sequence was 4436-bp long and possessed two open reading frames (ORF-1 and ORF-2) oriented in opposite directions. The putative proteins encoded by these two ORFs could not be characterized by comparison with the proteins of other species in the data banks. The presence of the ribonucleotide reductase small subunit (RNRS) gene at the 3′ end of the K1 region allowed us to determine that these two genes, RNRS and DPOL, are separated 5508 bp and oriented in the same direction in the genome of RSIV. Moreover, it is of interest that a
PstI-restriction fragment, of which the sequence but not the location within the RSIV genome had previously been reported, is located at nucleotide positions from 1096 to 2054, extending from within the ORF-1 region, spanning the intervening sequence between ORF-1 and ORF-2, and extending into the ORF-2 region. Various repeating sequences up to 86 bp were present at the 3′ ends of ORFs, especially within the nucleotide sequences at the 3′ terminus of ORF-2. No similarities were detected when the DNA sequences of the K1 region were compared to the DNA sequences of a repetitive element in the genome of other iridoviruses.</description><subject>Animal aquaculture</subject><subject>Animal productions</subject><subject>Aquaculture</subject><subject>Biological and medical sciences</subject><subject>Cassette ligation-mediated PCR</subject><subject>Chrysophrys major</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA homology</subject><subject>Fish</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene amplification</subject><subject>Genetics</subject><subject>Iridovirus</subject><subject>Marine</subject><subject>Microbiology</subject><subject>Pisciculture</subject><subject>Red sea bream</subject><subject>Repetitive element</subject><subject>Vertebrate aquaculture</subject><subject>Virology</subject><issn>0044-8486</issn><issn>1873-5622</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkV9rFTEQxUOp0Gv1IxQWQdGHrZM_m6RPUq5Vi0Uf1Ocwzc62KXuTNtkt6Kdv9t6i4EufMnB-c3I4w9gRh2MOXL__AaBUa5XVb0G8A-ikbWGPrbg1su20EPts9Rc5YM9LuQEArTu-YnF9jRn9RDn8wSmk2KShma6p-fjttImzHylNoaem0N1M0VNpQtzqVxTThhY6U19lbC4z4aYJOfTpPuS5LGxJI05Vr0tfU9VfsGcDjoVePr6H7Nens5_rL-3F98_n69OL1suTbmovez0MqAERpbQdKIvYKWkkESkvuPFeGE5mAI6q90IYpQX3qLHOgwZ5yN7sfG9zqsHL5DaheBpHjJTm4ri1SlngFXz1H3iT5hxrNidAGd4pKyrU7SCfUymZBnebwwbzb8fBLSdw2xO4pV8Hwm1P4JYUrx_NsXgch4zRh_JvWWlptFn8P-w4qpXcB8qu-LC03YdMfnJ9Ck_89ADR45r1</recordid><startdate>20030414</startdate><enddate>20030414</enddate><creator>Jeong, Joon Bum</creator><creator>Jun, Lyu Jin</creator><creator>Yoo, Min Ho</creator><creator>Kim, Myong Sug</creator><creator>Komisar, Jack L</creator><creator>Jeong, Hyun Do</creator><general>Elsevier B.V</general><general>Elsevier Science</general><general>Elsevier Sequoia S.A</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QR</scope><scope>7ST</scope><scope>7TN</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7TM</scope></search><sort><creationdate>20030414</creationdate><title>Characterization of the DNA nucleotide sequences in the genome of red sea bream iridoviruses isolated in Korea</title><author>Jeong, Joon Bum ; Jun, Lyu Jin ; Yoo, Min Ho ; Kim, Myong Sug ; Komisar, Jack L ; Jeong, Hyun Do</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-bd6ffa60aaa3385048aa54373eee4c217cc271e7f01a4dc2274621ca6ac22f603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animal aquaculture</topic><topic>Animal productions</topic><topic>Aquaculture</topic><topic>Biological and medical sciences</topic><topic>Cassette ligation-mediated PCR</topic><topic>Chrysophrys major</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA homology</topic><topic>Fish</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene amplification</topic><topic>Genetics</topic><topic>Iridovirus</topic><topic>Marine</topic><topic>Microbiology</topic><topic>Pisciculture</topic><topic>Red sea bream</topic><topic>Repetitive element</topic><topic>Vertebrate aquaculture</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeong, Joon Bum</creatorcontrib><creatorcontrib>Jun, Lyu Jin</creatorcontrib><creatorcontrib>Yoo, Min Ho</creatorcontrib><creatorcontrib>Kim, Myong Sug</creatorcontrib><creatorcontrib>Komisar, Jack L</creatorcontrib><creatorcontrib>Jeong, Hyun Do</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Aquaculture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeong, Joon Bum</au><au>Jun, Lyu Jin</au><au>Yoo, Min Ho</au><au>Kim, Myong Sug</au><au>Komisar, Jack L</au><au>Jeong, Hyun Do</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of the DNA nucleotide sequences in the genome of red sea bream iridoviruses isolated in Korea</atitle><jtitle>Aquaculture</jtitle><date>2003-04-14</date><risdate>2003</risdate><volume>220</volume><issue>1</issue><spage>119</spage><epage>133</epage><pages>119-133</pages><issn>0044-8486</issn><eissn>1873-5622</eissn><coden>AQCLAL</coden><abstract>The nucleotide sequences of DNA fragments amplified by polymerase chain reaction (PCR) from four different genomic regions of nine red sea bream iridoviruses (RSIVs) isolated from different species of fish, different areas and in different years in Korea were compared with the reported reference sequences. One isolate, RSIV Namhae, showed 100% homology to the reference sequences, while the other eight isolates, which appeared to contain identical nucleotide sequences, showed 96.6–98.9% homology with reference sequences depending upon the target regions of PCR gene amplification. However, differences in nucleotide sequences were not apparent between the RSIVs isolated in different locations, in different years or in different host species. We also cloned and sequenced the 3′ end flanking region (K1) of the DNA polymerase (DPOL) gene using the cassette ligation-mediated PCR method. This sequence was 4436-bp long and possessed two open reading frames (ORF-1 and ORF-2) oriented in opposite directions. The putative proteins encoded by these two ORFs could not be characterized by comparison with the proteins of other species in the data banks. The presence of the ribonucleotide reductase small subunit (RNRS) gene at the 3′ end of the K1 region allowed us to determine that these two genes, RNRS and DPOL, are separated 5508 bp and oriented in the same direction in the genome of RSIV. Moreover, it is of interest that a
PstI-restriction fragment, of which the sequence but not the location within the RSIV genome had previously been reported, is located at nucleotide positions from 1096 to 2054, extending from within the ORF-1 region, spanning the intervening sequence between ORF-1 and ORF-2, and extending into the ORF-2 region. Various repeating sequences up to 86 bp were present at the 3′ ends of ORFs, especially within the nucleotide sequences at the 3′ terminus of ORF-2. No similarities were detected when the DNA sequences of the K1 region were compared to the DNA sequences of a repetitive element in the genome of other iridoviruses.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/S0044-8486(02)00538-0</doi><tpages>15</tpages></addata></record> |
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subjects | Animal aquaculture Animal productions Aquaculture Biological and medical sciences Cassette ligation-mediated PCR Chrysophrys major Deoxyribonucleic acid DNA DNA homology Fish Fundamental and applied biological sciences. Psychology Gene amplification Genetics Iridovirus Marine Microbiology Pisciculture Red sea bream Repetitive element Vertebrate aquaculture Virology |
title | Characterization of the DNA nucleotide sequences in the genome of red sea bream iridoviruses isolated in Korea |
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