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AKR Murine Leukemia Virus Genome: Frequency of Sequences in DNA of High-, Low-, and Non-Virus-Yielding Mouse Strains
Studies with a single-stranded DNA probe complementary to the RNA of mouse-tropic AKR murine leukemia virus indicate that the complete genome of the AKR-type murine leukemia virus is present in the DNA of high- and low-virus-yielding mouse strains, while DNA of non-virus-yielding strains contains on...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1974-09, Vol.71 (9), p.3555-3559 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Lowy, Douglas R. Chattopadhyay, Sisir K. Teich, Natalie M. Rowe, Wallace P. Levine, Arthur S. |
description | Studies with a single-stranded DNA probe complementary to the RNA of mouse-tropic AKR murine leukemia virus indicate that the complete genome of the AKR-type murine leukemia virus is present in the DNA of high- and low-virus-yielding mouse strains, while DNA of non-virus-yielding strains contains only a part of the genome. Furthermore, in those strains where the genome is complete, two populations of virus-specific DNA sequences can be identified (more abundant and less abundant species) according to their rate of association with the probe. Low-virus-yielding mouse strains contain fewer copies of the less abundant species and, consequently, fewer complete viral genomes than do high-virus-yielding strains. Thus, in the ten strains tested, there is a good correlation between completeness of the genome of AKR-type murine leukemia virus in cellular DNA and the capacity of the cells to release infectious AKR-type murine leukemia virus. Moreover, the number of complete viral genomes correlates with the frequency of infectious virus production by virus-positive strains. DNA from wild Mus musculus also contained viral sequences, the sample tested showing reassociation kinetics identical to the non-virus-producing strains. |
doi_str_mv | 10.1073/pnas.71.9.3555 |
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Furthermore, in those strains where the genome is complete, two populations of virus-specific DNA sequences can be identified (more abundant and less abundant species) according to their rate of association with the probe. Low-virus-yielding mouse strains contain fewer copies of the less abundant species and, consequently, fewer complete viral genomes than do high-virus-yielding strains. Thus, in the ten strains tested, there is a good correlation between completeness of the genome of AKR-type murine leukemia virus in cellular DNA and the capacity of the cells to release infectious AKR-type murine leukemia virus. Moreover, the number of complete viral genomes correlates with the frequency of infectious virus production by virus-positive strains. 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Furthermore, in those strains where the genome is complete, two populations of virus-specific DNA sequences can be identified (more abundant and less abundant species) according to their rate of association with the probe. Low-virus-yielding mouse strains contain fewer copies of the less abundant species and, consequently, fewer complete viral genomes than do high-virus-yielding strains. Thus, in the ten strains tested, there is a good correlation between completeness of the genome of AKR-type murine leukemia virus in cellular DNA and the capacity of the cells to release infectious AKR-type murine leukemia virus. Moreover, the number of complete viral genomes correlates with the frequency of infectious virus production by virus-positive strains. DNA from wild Mus musculus also contained viral sequences, the sample tested showing reassociation kinetics identical to the non-virus-producing strains.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological Sciences: Biochemistry</subject><subject>Cots</subject><subject>DNA</subject><subject>DNA probes</subject><subject>DNA, Single-Stranded</subject><subject>DNA, Viral - metabolism</subject><subject>Embryos</subject><subject>Genomes</subject><subject>Genotype</subject><subject>Hybridity</subject><subject>Kinetics</subject><subject>Leukemia Virus, Murine - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred AKR</subject><subject>Murine leukemia virus</subject><subject>Nucleic Acid Hybridization</subject><subject>Phosphates</subject><subject>RNA, Viral</subject><subject>Temperature</subject><subject>Tritium</subject><subject>Virus Replication</subject><subject>Viruses</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1974</creationdate><recordtype>article</recordtype><recordid>eNptUU1rFDEYDqLUtXr1IAg5eXLGfM1HhB6WaltxW8Gq4ClkMu9sU2eSNZlR--_NuOuygpck5Pl6Xx6EnlKSU1LxVxunY17RXOa8KIp7aEGJpFkpJLmPFoSwKqsFEw_RoxhvCSGyqMkROhK8YiUTCzQu33_El1OwDvAKpm8wWI2_2DBFfA7OD_AanwX4PoEzd9h3-Hr7hoitw2-ulvPfhV3fZC_xyv9Mp3YtvvIu--ORfbXQt9at8aWfIuDrMWjr4mP0oNN9hCe7-xh9Pnv76fQiW304f3e6XGWGV7TIyk4LQZnsWNV2mum2YKQzvDHUSKo5r6FltGkqwwVjTdE1RLZSlkYI3UoQFT9GJ1vfzdQM0BpwKb9Xm2AHHe6U11b9izh7o9b-hxLJnPKkf7HTB5_WjqMabDTQ99pB2kfVrChqTkQi5luiCT7GAN0-gxI116TmmlRFlVRzTUnw_HCyPX3Xy0HyrPuL7vWqm_p-hF_jgdF_iQl_tsVv4-jDnlDyNDf_DSpUrzI</recordid><startdate>19740901</startdate><enddate>19740901</enddate><creator>Lowy, Douglas R.</creator><creator>Chattopadhyay, Sisir K.</creator><creator>Teich, Natalie M.</creator><creator>Rowe, Wallace P.</creator><creator>Levine, Arthur S.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19740901</creationdate><title>AKR Murine Leukemia Virus Genome: Frequency of Sequences in DNA of High-, Low-, and Non-Virus-Yielding Mouse Strains</title><author>Lowy, Douglas R. ; Chattopadhyay, Sisir K. ; Teich, Natalie M. ; Rowe, Wallace P. ; Levine, Arthur S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3715-6fa44129f27dfa2ad520fc3bc1c91a338ed21bb7c3422b5fb09d996c44ad9e473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1974</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological Sciences: Biochemistry</topic><topic>Cots</topic><topic>DNA</topic><topic>DNA probes</topic><topic>DNA, Single-Stranded</topic><topic>DNA, Viral - metabolism</topic><topic>Embryos</topic><topic>Genomes</topic><topic>Genotype</topic><topic>Hybridity</topic><topic>Kinetics</topic><topic>Leukemia Virus, Murine - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred AKR</topic><topic>Murine leukemia virus</topic><topic>Nucleic Acid Hybridization</topic><topic>Phosphates</topic><topic>RNA, Viral</topic><topic>Temperature</topic><topic>Tritium</topic><topic>Virus Replication</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lowy, Douglas R.</creatorcontrib><creatorcontrib>Chattopadhyay, Sisir K.</creatorcontrib><creatorcontrib>Teich, Natalie M.</creatorcontrib><creatorcontrib>Rowe, Wallace P.</creatorcontrib><creatorcontrib>Levine, Arthur S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lowy, Douglas R.</au><au>Chattopadhyay, Sisir K.</au><au>Teich, Natalie M.</au><au>Rowe, Wallace P.</au><au>Levine, Arthur S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AKR Murine Leukemia Virus Genome: Frequency of Sequences in DNA of High-, Low-, and Non-Virus-Yielding Mouse Strains</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1974-09-01</date><risdate>1974</risdate><volume>71</volume><issue>9</issue><spage>3555</spage><epage>3559</epage><pages>3555-3559</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Studies with a single-stranded DNA probe complementary to the RNA of mouse-tropic AKR murine leukemia virus indicate that the complete genome of the AKR-type murine leukemia virus is present in the DNA of high- and low-virus-yielding mouse strains, while DNA of non-virus-yielding strains contains only a part of the genome. Furthermore, in those strains where the genome is complete, two populations of virus-specific DNA sequences can be identified (more abundant and less abundant species) according to their rate of association with the probe. Low-virus-yielding mouse strains contain fewer copies of the less abundant species and, consequently, fewer complete viral genomes than do high-virus-yielding strains. Thus, in the ten strains tested, there is a good correlation between completeness of the genome of AKR-type murine leukemia virus in cellular DNA and the capacity of the cells to release infectious AKR-type murine leukemia virus. Moreover, the number of complete viral genomes correlates with the frequency of infectious virus production by virus-positive strains. 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subjects | Animals Base Sequence Biological Sciences: Biochemistry Cots DNA DNA probes DNA, Single-Stranded DNA, Viral - metabolism Embryos Genomes Genotype Hybridity Kinetics Leukemia Virus, Murine - metabolism Mice Mice, Inbred AKR Murine leukemia virus Nucleic Acid Hybridization Phosphates RNA, Viral Temperature Tritium Virus Replication Viruses |
title | AKR Murine Leukemia Virus Genome: Frequency of Sequences in DNA of High-, Low-, and Non-Virus-Yielding Mouse Strains |
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