ART-CH: a VL30 in chickens?

The complete sequence of ART-CH, a recently found chicken retrotransposon (A.V. Gudkov, E.A. Komarova, M.A. Nikiforov, and T.E. Zaitsevskaya, J. Virol. 66:1726-1736,1992), was characterized. ART-CH has the structure of a 3,300-bp-long provirus, including two 388-bp long terminal repeats (LTRs) (U3,...

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Veröffentlicht in:Journal of Virology 1994-02, Vol.68 (2), p.846-853
Hauptverfasser: Nikiforov, M.A, Gudkov, A.V
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description The complete sequence of ART-CH, a recently found chicken retrotransposon (A.V. Gudkov, E.A. Komarova, M.A. Nikiforov, and T.E. Zaitsevskaya, J. Virol. 66:1726-1736,1992), was characterized. ART-CH has the structure of a 3,300-bp-long provirus, including two 388-bp long terminal repeats (LTRs) (U3, 245 bp; R region, 17 bp; and U5, 126 bp), a tRNA(Trp)p-binding site, and a polypurine tract, similar to avian leukosis viruses. At least some of the approximately 50 genomic copies of ART-CH are transcribed into polyadenylated RNA, which is initiated and terminated at the expected sites within the LTRs. In contrast to the regulatory sequences involved in proviral expression and replication, the internal regions of ART-CH seem to be completely defective. Several short regions of homology with avian leukosis virus genes, most of which encode gag-related sequences, were found among different reading frames of ART-CH, which are not organized like regular retroviral genes. Both sequence analysis and restriction fragment length polymorphism analysis revealed a high degree of sequence (97% homology) and structural similarity among members of the ART-CH family, indicating their common origin and recent penetration into chicken DNA. ART-CH sequences were detected in mouse cells infected with Rous sarcoma virus produced by an ART-CH-expressing Rous sarcoma. These data are consistent with the hypothesis that ART-CH belongs to a class of defective retrotransposons whose replication strategy requires the use of helper viruses. They might originate from an avian leukosis virus-related retrovirus which completely lost its coding capacities as a result of multiple mutations and deletions. These features apparently group ART-CH with the VL30 retrotransposons of rodents
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Gudkov, E.A. Komarova, M.A. Nikiforov, and T.E. Zaitsevskaya, J. Virol. 66:1726-1736,1992), was characterized. ART-CH has the structure of a 3,300-bp-long provirus, including two 388-bp long terminal repeats (LTRs) (U3, 245 bp; R region, 17 bp; and U5, 126 bp), a tRNA(Trp)p-binding site, and a polypurine tract, similar to avian leukosis viruses. At least some of the approximately 50 genomic copies of ART-CH are transcribed into polyadenylated RNA, which is initiated and terminated at the expected sites within the LTRs. In contrast to the regulatory sequences involved in proviral expression and replication, the internal regions of ART-CH seem to be completely defective. Several short regions of homology with avian leukosis virus genes, most of which encode gag-related sequences, were found among different reading frames of ART-CH, which are not organized like regular retroviral genes. Both sequence analysis and restriction fragment length polymorphism analysis revealed a high degree of sequence (97% homology) and structural similarity among members of the ART-CH family, indicating their common origin and recent penetration into chicken DNA. ART-CH sequences were detected in mouse cells infected with Rous sarcoma virus produced by an ART-CH-expressing Rous sarcoma. These data are consistent with the hypothesis that ART-CH belongs to a class of defective retrotransposons whose replication strategy requires the use of helper viruses. They might originate from an avian leukosis virus-related retrovirus which completely lost its coding capacities as a result of multiple mutations and deletions. 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Gudkov, E.A. Komarova, M.A. Nikiforov, and T.E. Zaitsevskaya, J. Virol. 66:1726-1736,1992), was characterized. ART-CH has the structure of a 3,300-bp-long provirus, including two 388-bp long terminal repeats (LTRs) (U3, 245 bp; R region, 17 bp; and U5, 126 bp), a tRNA(Trp)p-binding site, and a polypurine tract, similar to avian leukosis viruses. At least some of the approximately 50 genomic copies of ART-CH are transcribed into polyadenylated RNA, which is initiated and terminated at the expected sites within the LTRs. In contrast to the regulatory sequences involved in proviral expression and replication, the internal regions of ART-CH seem to be completely defective. Several short regions of homology with avian leukosis virus genes, most of which encode gag-related sequences, were found among different reading frames of ART-CH, which are not organized like regular retroviral genes. Both sequence analysis and restriction fragment length polymorphism analysis revealed a high degree of sequence (97% homology) and structural similarity among members of the ART-CH family, indicating their common origin and recent penetration into chicken DNA. ART-CH sequences were detected in mouse cells infected with Rous sarcoma virus produced by an ART-CH-expressing Rous sarcoma. These data are consistent with the hypothesis that ART-CH belongs to a class of defective retrotransposons whose replication strategy requires the use of helper viruses. They might originate from an avian leukosis virus-related retrovirus which completely lost its coding capacities as a result of multiple mutations and deletions. 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Gudkov, A.V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-2c5d3055b590d0159b91424ca9e74ad601c81a2c0d5228d9bd1a076f1d3d70763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>ADN</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>avian leukosis virus</topic><topic>Base Sequence</topic><topic>Biological Evolution</topic><topic>Cells, Cultured</topic><topic>Chickens - genetics</topic><topic>Defective Viruses - genetics</topic><topic>DNA Transposable Elements - genetics</topic><topic>Molecular Sequence Data</topic><topic>ONCOVIRUS AVIAIRE</topic><topic>ONCOVIRUS AVIAR</topic><topic>POLIMORFISMO</topic><topic>POLLO</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>POLYMORPHISME</topic><topic>POULET</topic><topic>Proviruses - genetics</topic><topic>Retroviridae - genetics</topic><topic>SECUENCIA NUCLEICA</topic><topic>Sequence Analysis, DNA</topic><topic>Sequence Homology, Amino Acid</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>SEQUENCE NUCLEIQUE</topic><topic>Time Factors</topic><topic>Transcription, Genetic</topic><topic>VIRUS DE LOS ANIMALES</topic><topic>VIRUS DES ANIMAUX</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nikiforov, M.A</creatorcontrib><creatorcontrib>Gudkov, A.V</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>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nikiforov, M.A</au><au>Gudkov, A.V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ART-CH: a VL30 in chickens?</atitle><jtitle>Journal of Virology</jtitle><addtitle>J Virol</addtitle><date>1994-02-01</date><risdate>1994</risdate><volume>68</volume><issue>2</issue><spage>846</spage><epage>853</epage><pages>846-853</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>The complete sequence of ART-CH, a recently found chicken retrotransposon (A.V. Gudkov, E.A. Komarova, M.A. Nikiforov, and T.E. Zaitsevskaya, J. Virol. 66:1726-1736,1992), was characterized. ART-CH has the structure of a 3,300-bp-long provirus, including two 388-bp long terminal repeats (LTRs) (U3, 245 bp; R region, 17 bp; and U5, 126 bp), a tRNA(Trp)p-binding site, and a polypurine tract, similar to avian leukosis viruses. At least some of the approximately 50 genomic copies of ART-CH are transcribed into polyadenylated RNA, which is initiated and terminated at the expected sites within the LTRs. In contrast to the regulatory sequences involved in proviral expression and replication, the internal regions of ART-CH seem to be completely defective. Several short regions of homology with avian leukosis virus genes, most of which encode gag-related sequences, were found among different reading frames of ART-CH, which are not organized like regular retroviral genes. Both sequence analysis and restriction fragment length polymorphism analysis revealed a high degree of sequence (97% homology) and structural similarity among members of the ART-CH family, indicating their common origin and recent penetration into chicken DNA. ART-CH sequences were detected in mouse cells infected with Rous sarcoma virus produced by an ART-CH-expressing Rous sarcoma. These data are consistent with the hypothesis that ART-CH belongs to a class of defective retrotransposons whose replication strategy requires the use of helper viruses. They might originate from an avian leukosis virus-related retrovirus which completely lost its coding capacities as a result of multiple mutations and deletions. These features apparently group ART-CH with the VL30 retrotransposons of rodents</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>7904657</pmid><doi>10.1128/jvi.68.2.846-853.1994</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects ADN
Amino Acid Sequence
Animals
avian leukosis virus
Base Sequence
Biological Evolution
Cells, Cultured
Chickens - genetics
Defective Viruses - genetics
DNA Transposable Elements - genetics
Molecular Sequence Data
ONCOVIRUS AVIAIRE
ONCOVIRUS AVIAR
POLIMORFISMO
POLLO
Polymorphism, Restriction Fragment Length
POLYMORPHISME
POULET
Proviruses - genetics
Retroviridae - genetics
SECUENCIA NUCLEICA
Sequence Analysis, DNA
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
SEQUENCE NUCLEIQUE
Time Factors
Transcription, Genetic
VIRUS DE LOS ANIMALES
VIRUS DES ANIMAUX
title ART-CH: a VL30 in chickens?
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