Amplification and Molecular Cloning of HTLV-I Sequences from DNA of Multiple Sclerosis Patients

Techniques of gene amplification, molecular cloning, and sequence analysis were used to test for the presence of sequences related to human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells of six patients with multiple sclerosis (MS) and 20 normal individuals. HTLV-I sequen...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Science (American Association for the Advancement of Science) 1989-01, Vol.243 (4890), p.529-533
Hauptverfasser: Reddy, E. Premkumar, Sandberg-Wollheim, Magnhild, Mettus, Richard V., Ray, Phillip E., DeFreitas, Elaine, Koprowski, Hilary
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 533
container_issue 4890
container_start_page 529
container_title Science (American Association for the Advancement of Science)
container_volume 243
creator Reddy, E. Premkumar
Sandberg-Wollheim, Magnhild
Mettus, Richard V.
Ray, Phillip E.
DeFreitas, Elaine
Koprowski, Hilary
description Techniques of gene amplification, molecular cloning, and sequence analysis were used to test for the presence of sequences related to human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells of six patients with multiple sclerosis (MS) and 20 normal individuals. HTLV-I sequences were detected in all six MS patients and in one individual from the control group by DNA blot analysis and molecular cloning of amplified DNAs. The viral sequences in MS patients were associated with adherent cell populations consisting predominantly of monocytes and macrophages. Molecular cloning and nucleotide sequence analysis indicated that these amplified viral sequences were related to the HTLV-I proviral genome.
doi_str_mv 10.1126/science.2536193
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_78845302</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A7029426</galeid><jstor_id>1703222</jstor_id><sourcerecordid>A7029426</sourcerecordid><originalsourceid>FETCH-LOGICAL-c729t-8ce44604c76a5123528ef2c2b1429d45507d7cd9948c8fa26575b78fa4afdbdc3</originalsourceid><addsrcrecordid>eNqN081v0zAUAHALgUYpnLmAFE0IDiObP-P4WAp0lboVqWPXyHWcyJUTFzuR4L_HVaNtoEqtcnCU9_Nz7PcMwFsELxHC2VVQRrdKX2JGMiTIMzBCULBUYEiegxGEJEtzyNlL8CqEDYQxJsgZOBv4CBSTZmtNZZTsjGsT2ZbJjbNa9Vb6ZGpda9o6cVVyfbe4T-fJSv_qd-uFpPKuSb7eTnbBm952Zmt1slJWexdMSH7EfLrtwmvwopI26DfDOAY_v3-7m16ni-VsPp0sUsWx6NJcaUozSBXPJEOYMJzrCiu8RhSLkjIGeclVKQTNVV5JnDHO1jy-UVmV61KRMfi4z7v1Lv5i6IrGBKWtla12fSh4nlNGID4KSUZzTDE9CjFCnAtyPCNiCCEieITn_8GN630bjyUmIyzuNJZkDC72qJZWF6atXOelqnWrvYzl0JWJnyccYkFxFvXnAzo-pW6MOsA__cOj6PTvrpZ9CMV8dXuqXN6fKr_MTpT5bPFUXhySylmra13Ezpkun-qrvVax94LXVbH1ppH-T4FgsbslxXBLiqHt44z3QyX6daPLB_8Y_zDEZVDSVl62yoQHxgnkNJZsDN7t2SZ0zj-uyiHBGJO_AuQeUw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213542919</pqid></control><display><type>article</type><title>Amplification and Molecular Cloning of HTLV-I Sequences from DNA of Multiple Sclerosis Patients</title><source>American Association for the Advancement of Science</source><source>Jstor Complete Legacy</source><source>MEDLINE</source><creator>Reddy, E. Premkumar ; Sandberg-Wollheim, Magnhild ; Mettus, Richard V. ; Ray, Phillip E. ; DeFreitas, Elaine ; Koprowski, Hilary</creator><creatorcontrib>Reddy, E. Premkumar ; Sandberg-Wollheim, Magnhild ; Mettus, Richard V. ; Ray, Phillip E. ; DeFreitas, Elaine ; Koprowski, Hilary</creatorcontrib><description>Techniques of gene amplification, molecular cloning, and sequence analysis were used to test for the presence of sequences related to human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells of six patients with multiple sclerosis (MS) and 20 normal individuals. HTLV-I sequences were detected in all six MS patients and in one individual from the control group by DNA blot analysis and molecular cloning of amplified DNAs. The viral sequences in MS patients were associated with adherent cell populations consisting predominantly of monocytes and macrophages. Molecular cloning and nucleotide sequence analysis indicated that these amplified viral sequences were related to the HTLV-I proviral genome.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.2536193</identifier><identifier>PMID: 2536193</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington, DC: The American Association for the Advancement of Science</publisher><subject>Adolescent ; Adult ; AIDS/HIV ; Analysis ; Antibodies ; Base Sequence ; Biological and medical sciences ; Blood cells ; Cell lines ; Child ; Cloning, Molecular ; DNA ; DNA Restriction Enzymes ; DNA, Viral - genetics ; Female ; Gene Amplification ; Genetic aspects ; Genetics ; Genomes ; HIV ; HIV (Viruses) ; Human T lymphotropic virus 1 ; Human T-lymphotropic virus 1 - genetics ; Humans ; Leukocytes ; Leukocytes, Mononuclear - analysis ; Leukocytes, Mononuclear - microbiology ; Lymphocytes ; Macrophages - analysis ; Macrophages - microbiology ; Male ; Medical research ; Medical sciences ; Molecular Sequence Data ; Monocytes ; Multiple sclerosis ; Multiple Sclerosis - microbiology ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurology ; Nucleic Acid Hybridization ; Oligonucleotide Probes ; Plasmids ; T lymphocytes ; Tests ; Viruses</subject><ispartof>Science (American Association for the Advancement of Science), 1989-01, Vol.243 (4890), p.529-533</ispartof><rights>Copyright 1989 The American Association for the Advancement of Science</rights><rights>1989 INIST-CNRS</rights><rights>COPYRIGHT 1989 American Association for the Advancement of Science</rights><rights>COPYRIGHT 1989 American Association for the Advancement of Science</rights><rights>Copyright American Association for the Advancement of Science Jan 27, 1989</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c729t-8ce44604c76a5123528ef2c2b1429d45507d7cd9948c8fa26575b78fa4afdbdc3</citedby><cites>FETCH-LOGICAL-c729t-8ce44604c76a5123528ef2c2b1429d45507d7cd9948c8fa26575b78fa4afdbdc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1703222$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1703222$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,2871,2872,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=7307421$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2536193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reddy, E. Premkumar</creatorcontrib><creatorcontrib>Sandberg-Wollheim, Magnhild</creatorcontrib><creatorcontrib>Mettus, Richard V.</creatorcontrib><creatorcontrib>Ray, Phillip E.</creatorcontrib><creatorcontrib>DeFreitas, Elaine</creatorcontrib><creatorcontrib>Koprowski, Hilary</creatorcontrib><title>Amplification and Molecular Cloning of HTLV-I Sequences from DNA of Multiple Sclerosis Patients</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>Techniques of gene amplification, molecular cloning, and sequence analysis were used to test for the presence of sequences related to human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells of six patients with multiple sclerosis (MS) and 20 normal individuals. HTLV-I sequences were detected in all six MS patients and in one individual from the control group by DNA blot analysis and molecular cloning of amplified DNAs. The viral sequences in MS patients were associated with adherent cell populations consisting predominantly of monocytes and macrophages. Molecular cloning and nucleotide sequence analysis indicated that these amplified viral sequences were related to the HTLV-I proviral genome.</description><subject>Adolescent</subject><subject>Adult</subject><subject>AIDS/HIV</subject><subject>Analysis</subject><subject>Antibodies</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Blood cells</subject><subject>Cell lines</subject><subject>Child</subject><subject>Cloning, Molecular</subject><subject>DNA</subject><subject>DNA Restriction Enzymes</subject><subject>DNA, Viral - genetics</subject><subject>Female</subject><subject>Gene Amplification</subject><subject>Genetic aspects</subject><subject>Genetics</subject><subject>Genomes</subject><subject>HIV</subject><subject>HIV (Viruses)</subject><subject>Human T lymphotropic virus 1</subject><subject>Human T-lymphotropic virus 1 - genetics</subject><subject>Humans</subject><subject>Leukocytes</subject><subject>Leukocytes, Mononuclear - analysis</subject><subject>Leukocytes, Mononuclear - microbiology</subject><subject>Lymphocytes</subject><subject>Macrophages - analysis</subject><subject>Macrophages - microbiology</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Monocytes</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - microbiology</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurology</subject><subject>Nucleic Acid Hybridization</subject><subject>Oligonucleotide Probes</subject><subject>Plasmids</subject><subject>T lymphocytes</subject><subject>Tests</subject><subject>Viruses</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN081v0zAUAHALgUYpnLmAFE0IDiObP-P4WAp0lboVqWPXyHWcyJUTFzuR4L_HVaNtoEqtcnCU9_Nz7PcMwFsELxHC2VVQRrdKX2JGMiTIMzBCULBUYEiegxGEJEtzyNlL8CqEDYQxJsgZOBv4CBSTZmtNZZTsjGsT2ZbJjbNa9Vb6ZGpda9o6cVVyfbe4T-fJSv_qd-uFpPKuSb7eTnbBm952Zmt1slJWexdMSH7EfLrtwmvwopI26DfDOAY_v3-7m16ni-VsPp0sUsWx6NJcaUozSBXPJEOYMJzrCiu8RhSLkjIGeclVKQTNVV5JnDHO1jy-UVmV61KRMfi4z7v1Lv5i6IrGBKWtla12fSh4nlNGID4KSUZzTDE9CjFCnAtyPCNiCCEieITn_8GN630bjyUmIyzuNJZkDC72qJZWF6atXOelqnWrvYzl0JWJnyccYkFxFvXnAzo-pW6MOsA__cOj6PTvrpZ9CMV8dXuqXN6fKr_MTpT5bPFUXhySylmra13Ezpkun-qrvVax94LXVbH1ppH-T4FgsbslxXBLiqHt44z3QyX6daPLB_8Y_zDEZVDSVl62yoQHxgnkNJZsDN7t2SZ0zj-uyiHBGJO_AuQeUw</recordid><startdate>19890127</startdate><enddate>19890127</enddate><creator>Reddy, E. Premkumar</creator><creator>Sandberg-Wollheim, Magnhild</creator><creator>Mettus, Richard V.</creator><creator>Ray, Phillip E.</creator><creator>DeFreitas, Elaine</creator><creator>Koprowski, Hilary</creator><general>The American Association for the Advancement of Science</general><general>American Association for the Advancement of Science</general><scope>IQODW</scope><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>8GL</scope><scope>IBG</scope><scope>IOV</scope><scope>ISN</scope><scope>0-V</scope><scope>3V.</scope><scope>7QF</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QQ</scope><scope>7QR</scope><scope>7SC</scope><scope>7SE</scope><scope>7SN</scope><scope>7SP</scope><scope>7SR</scope><scope>7SS</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9-</scope><scope>K9.</scope><scope>KB.</scope><scope>KR7</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>L~C</scope><scope>L~D</scope><scope>M0K</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19890127</creationdate><title>Amplification and Molecular Cloning of HTLV-I Sequences from DNA of Multiple Sclerosis Patients</title><author>Reddy, E. Premkumar ; Sandberg-Wollheim, Magnhild ; Mettus, Richard V. ; Ray, Phillip E. ; DeFreitas, Elaine ; Koprowski, Hilary</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c729t-8ce44604c76a5123528ef2c2b1429d45507d7cd9948c8fa26575b78fa4afdbdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>AIDS/HIV</topic><topic>Analysis</topic><topic>Antibodies</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Blood cells</topic><topic>Cell lines</topic><topic>Child</topic><topic>Cloning, Molecular</topic><topic>DNA</topic><topic>DNA Restriction Enzymes</topic><topic>DNA, Viral - genetics</topic><topic>Female</topic><topic>Gene Amplification</topic><topic>Genetic aspects</topic><topic>Genetics</topic><topic>Genomes</topic><topic>HIV</topic><topic>HIV (Viruses)</topic><topic>Human T lymphotropic virus 1</topic><topic>Human T-lymphotropic virus 1 - genetics</topic><topic>Humans</topic><topic>Leukocytes</topic><topic>Leukocytes, Mononuclear - analysis</topic><topic>Leukocytes, Mononuclear - microbiology</topic><topic>Lymphocytes</topic><topic>Macrophages - analysis</topic><topic>Macrophages - microbiology</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Molecular Sequence Data</topic><topic>Monocytes</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - microbiology</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurology</topic><topic>Nucleic Acid Hybridization</topic><topic>Oligonucleotide Probes</topic><topic>Plasmids</topic><topic>T lymphocytes</topic><topic>Tests</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reddy, E. Premkumar</creatorcontrib><creatorcontrib>Sandberg-Wollheim, Magnhild</creatorcontrib><creatorcontrib>Mettus, Richard V.</creatorcontrib><creatorcontrib>Ray, Phillip E.</creatorcontrib><creatorcontrib>DeFreitas, Elaine</creatorcontrib><creatorcontrib>Koprowski, Hilary</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>Gale In Context: Biography</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Aluminium Industry Abstracts</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Ecology Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric &amp; Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Civil Engineering Abstracts</collection><collection>ProQuest Engineering Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Agricultural Science Database</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric &amp; Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reddy, E. Premkumar</au><au>Sandberg-Wollheim, Magnhild</au><au>Mettus, Richard V.</au><au>Ray, Phillip E.</au><au>DeFreitas, Elaine</au><au>Koprowski, Hilary</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amplification and Molecular Cloning of HTLV-I Sequences from DNA of Multiple Sclerosis Patients</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1989-01-27</date><risdate>1989</risdate><volume>243</volume><issue>4890</issue><spage>529</spage><epage>533</epage><pages>529-533</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>Techniques of gene amplification, molecular cloning, and sequence analysis were used to test for the presence of sequences related to human T-lymphotropic virus type I (HTLV-I) in peripheral blood mononuclear cells of six patients with multiple sclerosis (MS) and 20 normal individuals. HTLV-I sequences were detected in all six MS patients and in one individual from the control group by DNA blot analysis and molecular cloning of amplified DNAs. The viral sequences in MS patients were associated with adherent cell populations consisting predominantly of monocytes and macrophages. Molecular cloning and nucleotide sequence analysis indicated that these amplified viral sequences were related to the HTLV-I proviral genome.</abstract><cop>Washington, DC</cop><pub>The American Association for the Advancement of Science</pub><pmid>2536193</pmid><doi>10.1126/science.2536193</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0036-8075
ispartof Science (American Association for the Advancement of Science), 1989-01, Vol.243 (4890), p.529-533
issn 0036-8075
1095-9203
language eng
recordid cdi_proquest_miscellaneous_78845302
source American Association for the Advancement of Science; Jstor Complete Legacy; MEDLINE
subjects Adolescent
Adult
AIDS/HIV
Analysis
Antibodies
Base Sequence
Biological and medical sciences
Blood cells
Cell lines
Child
Cloning, Molecular
DNA
DNA Restriction Enzymes
DNA, Viral - genetics
Female
Gene Amplification
Genetic aspects
Genetics
Genomes
HIV
HIV (Viruses)
Human T lymphotropic virus 1
Human T-lymphotropic virus 1 - genetics
Humans
Leukocytes
Leukocytes, Mononuclear - analysis
Leukocytes, Mononuclear - microbiology
Lymphocytes
Macrophages - analysis
Macrophages - microbiology
Male
Medical research
Medical sciences
Molecular Sequence Data
Monocytes
Multiple sclerosis
Multiple Sclerosis - microbiology
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
Neurology
Nucleic Acid Hybridization
Oligonucleotide Probes
Plasmids
T lymphocytes
Tests
Viruses
title Amplification and Molecular Cloning of HTLV-I Sequences from DNA of Multiple Sclerosis Patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T17%3A24%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amplification%20and%20Molecular%20Cloning%20of%20HTLV-I%20Sequences%20from%20DNA%20of%20Multiple%20Sclerosis%20Patients&rft.jtitle=Science%20(American%20Association%20for%20the%20Advancement%20of%20Science)&rft.au=Reddy,%20E.%20Premkumar&rft.date=1989-01-27&rft.volume=243&rft.issue=4890&rft.spage=529&rft.epage=533&rft.pages=529-533&rft.issn=0036-8075&rft.eissn=1095-9203&rft.coden=SCIEAS&rft_id=info:doi/10.1126/science.2536193&rft_dat=%3Cgale_proqu%3EA7029426%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=213542919&rft_id=info:pmid/2536193&rft_galeid=A7029426&rft_jstor_id=1703222&rfr_iscdi=true