Two alternating structures of the HIV-1 leader RNA
In this study we demonstrate that the HIV-1 leader RNA exists in two alternative conformations, a branched structure consisting of several well-known hairpin motifs and a more stable structure that is formed by extensive long-distance base pairing. The latter conformation was first identified as a c...
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Veröffentlicht in: | RNA (Cambridge) 2001-01, Vol.7 (1), p.143-157, Article S1355838201001881 |
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description | In this study we demonstrate that the HIV-1 leader
RNA exists in two alternative conformations, a branched
structure consisting of several well-known hairpin motifs
and a more stable structure that is formed by extensive
long-distance base pairing. The latter conformation was
first identified as a compactly folded RNA that migrates
unusually fast in nondenaturing gels. The minimally required
domains for formation of this conformer were determined
by mutational analysis. The poly(A) and DIS regions of
the leader are the major determinants of this RNA conformation.
Further biochemical characterization of this conformer
revealed that both hairpins are disrupted to allow extensive
long-distance base pairing. As the DIS hairpin is known
to be instrumental for formation of the HIV-1 RNA dimer,
the interplay between formation of the conformer and dimerization
was addressed. Formation of the conformer and the RNA dimer
are mutually exclusive. Consequently, the conformer must
rearrange into a branched structure that exposes the dimer
initiation signal (DIS) hairpin, thus triggering formation
of the RNA dimer. This structural rearrangement is facilitated
by the viral nucleocapsid protein NC. We propose that this
structural polymorphism of the HIV-1 leader RNA acts as
a molecular switch in the viral replication cycle. |
doi_str_mv | 10.1017/S1355838201001881 |
format | Article |
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RNA exists in two alternative conformations, a branched
structure consisting of several well-known hairpin motifs
and a more stable structure that is formed by extensive
long-distance base pairing. The latter conformation was
first identified as a compactly folded RNA that migrates
unusually fast in nondenaturing gels. The minimally required
domains for formation of this conformer were determined
by mutational analysis. The poly(A) and DIS regions of
the leader are the major determinants of this RNA conformation.
Further biochemical characterization of this conformer
revealed that both hairpins are disrupted to allow extensive
long-distance base pairing. As the DIS hairpin is known
to be instrumental for formation of the HIV-1 RNA dimer,
the interplay between formation of the conformer and dimerization
was addressed. Formation of the conformer and the RNA dimer
are mutually exclusive. Consequently, the conformer must
rearrange into a branched structure that exposes the dimer
initiation signal (DIS) hairpin, thus triggering formation
of the RNA dimer. This structural rearrangement is facilitated
by the viral nucleocapsid protein NC. We propose that this
structural polymorphism of the HIV-1 leader RNA acts as
a molecular switch in the viral replication cycle.</description><identifier>ISSN: 1355-8382</identifier><identifier>EISSN: 1469-9001</identifier><identifier>DOI: 10.1017/S1355838201001881</identifier><identifier>PMID: 11214176</identifier><language>eng</language><publisher>United States: Cambridge University Press</publisher><subject>Alternative Splicing ; Base Sequence ; dimer initiation site ; Dimerization ; HIV-1 - genetics ; Hot Temperature ; Human immunodeficiency virus 1 ; Humans ; leader RNA ; Models, Molecular ; Molecular Sequence Data ; Mutagenesis ; Nucleic Acid Conformation ; Nucleic Acid Denaturation ; nucleocapsid protein ; Poly A ; Proviruses - genetics ; RNA, Spliced Leader - chemistry ; RNA, Spliced Leader - genetics ; RNA, Viral - chemistry ; RNA, Viral - genetics ; Sequence Deletion ; Thermodynamics</subject><ispartof>RNA (Cambridge), 2001-01, Vol.7 (1), p.143-157, Article S1355838201001881</ispartof><rights>2001 RNA Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-5d5eb3c001438d2f9eeb85d8a00f5b25e96bd2f138fd332debd612a7bf209ae53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1370064/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1370064/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11214176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HUTHOFF, HENDRIK</creatorcontrib><creatorcontrib>BERKHOUT, BEN</creatorcontrib><title>Two alternating structures of the HIV-1 leader RNA</title><title>RNA (Cambridge)</title><addtitle>RNA</addtitle><description>In this study we demonstrate that the HIV-1 leader
RNA exists in two alternative conformations, a branched
structure consisting of several well-known hairpin motifs
and a more stable structure that is formed by extensive
long-distance base pairing. The latter conformation was
first identified as a compactly folded RNA that migrates
unusually fast in nondenaturing gels. The minimally required
domains for formation of this conformer were determined
by mutational analysis. The poly(A) and DIS regions of
the leader are the major determinants of this RNA conformation.
Further biochemical characterization of this conformer
revealed that both hairpins are disrupted to allow extensive
long-distance base pairing. As the DIS hairpin is known
to be instrumental for formation of the HIV-1 RNA dimer,
the interplay between formation of the conformer and dimerization
was addressed. Formation of the conformer and the RNA dimer
are mutually exclusive. Consequently, the conformer must
rearrange into a branched structure that exposes the dimer
initiation signal (DIS) hairpin, thus triggering formation
of the RNA dimer. This structural rearrangement is facilitated
by the viral nucleocapsid protein NC. We propose that this
structural polymorphism of the HIV-1 leader RNA acts as
a molecular switch in the viral replication cycle.</description><subject>Alternative Splicing</subject><subject>Base Sequence</subject><subject>dimer initiation site</subject><subject>Dimerization</subject><subject>HIV-1 - genetics</subject><subject>Hot Temperature</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>leader RNA</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis</subject><subject>Nucleic Acid Conformation</subject><subject>Nucleic Acid Denaturation</subject><subject>nucleocapsid protein</subject><subject>Poly A</subject><subject>Proviruses - genetics</subject><subject>RNA, Spliced Leader - chemistry</subject><subject>RNA, Spliced Leader - genetics</subject><subject>RNA, Viral - chemistry</subject><subject>RNA, Viral - genetics</subject><subject>Sequence Deletion</subject><subject>Thermodynamics</subject><issn>1355-8382</issn><issn>1469-9001</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF9LwzAUxYMobk4_gC_SJ9-quU3Tpi_CEHWDoaDT15A2t1tH184kVfz2Zqz4B8Gnm3vPub8bDiGnQC-AQnr5BIxzwUREgVIQAvbIEOIkCzPf7vu3l8OtPiBH1q78kHn5kAwAIoghTYYkmr-3gaodmka5qlkE1pmucJ1BG7Rl4JYYTKYvIQQ1Ko0meLwfH5ODUtUWT_o6Is-3N_PrSTh7uJtej2dhwVniQq455qzwR2MmdFRmiLngWihKS55HHLMk92NgotSMRRpznUCk0ryMaKaQsxG52nE3Xb5GXWDjjKrlxlRrZT5kqyr5W2mqpVy0bxJYSmkSe8B5DzDta4fWyXVlC6xr1WDbWQmp4CKOwRthZyxMa63B8usIULlNWv5J2u-c_fzd90YfrTewHqrWuan0AuWq7XzMtf0H-wnPEofs</recordid><startdate>200101</startdate><enddate>200101</enddate><creator>HUTHOFF, HENDRIK</creator><creator>BERKHOUT, BEN</creator><general>Cambridge University Press</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>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>200101</creationdate><title>Two alternating structures of the HIV-1 leader RNA</title><author>HUTHOFF, HENDRIK ; BERKHOUT, BEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-5d5eb3c001438d2f9eeb85d8a00f5b25e96bd2f138fd332debd612a7bf209ae53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Alternative Splicing</topic><topic>Base Sequence</topic><topic>dimer initiation site</topic><topic>Dimerization</topic><topic>HIV-1 - genetics</topic><topic>Hot Temperature</topic><topic>Human immunodeficiency virus 1</topic><topic>Humans</topic><topic>leader RNA</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis</topic><topic>Nucleic Acid Conformation</topic><topic>Nucleic Acid Denaturation</topic><topic>nucleocapsid protein</topic><topic>Poly A</topic><topic>Proviruses - genetics</topic><topic>RNA, Spliced Leader - chemistry</topic><topic>RNA, Spliced Leader - genetics</topic><topic>RNA, Viral - chemistry</topic><topic>RNA, Viral - genetics</topic><topic>Sequence Deletion</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HUTHOFF, HENDRIK</creatorcontrib><creatorcontrib>BERKHOUT, BEN</creatorcontrib><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>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RNA (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HUTHOFF, HENDRIK</au><au>BERKHOUT, BEN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two alternating structures of the HIV-1 leader RNA</atitle><jtitle>RNA (Cambridge)</jtitle><addtitle>RNA</addtitle><date>2001-01</date><risdate>2001</risdate><volume>7</volume><issue>1</issue><spage>143</spage><epage>157</epage><pages>143-157</pages><artnum>S1355838201001881</artnum><issn>1355-8382</issn><eissn>1469-9001</eissn><abstract>In this study we demonstrate that the HIV-1 leader
RNA exists in two alternative conformations, a branched
structure consisting of several well-known hairpin motifs
and a more stable structure that is formed by extensive
long-distance base pairing. The latter conformation was
first identified as a compactly folded RNA that migrates
unusually fast in nondenaturing gels. The minimally required
domains for formation of this conformer were determined
by mutational analysis. The poly(A) and DIS regions of
the leader are the major determinants of this RNA conformation.
Further biochemical characterization of this conformer
revealed that both hairpins are disrupted to allow extensive
long-distance base pairing. As the DIS hairpin is known
to be instrumental for formation of the HIV-1 RNA dimer,
the interplay between formation of the conformer and dimerization
was addressed. Formation of the conformer and the RNA dimer
are mutually exclusive. Consequently, the conformer must
rearrange into a branched structure that exposes the dimer
initiation signal (DIS) hairpin, thus triggering formation
of the RNA dimer. This structural rearrangement is facilitated
by the viral nucleocapsid protein NC. We propose that this
structural polymorphism of the HIV-1 leader RNA acts as
a molecular switch in the viral replication cycle.</abstract><cop>United States</cop><pub>Cambridge University Press</pub><pmid>11214176</pmid><doi>10.1017/S1355838201001881</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Alternative Splicing Base Sequence dimer initiation site Dimerization HIV-1 - genetics Hot Temperature Human immunodeficiency virus 1 Humans leader RNA Models, Molecular Molecular Sequence Data Mutagenesis Nucleic Acid Conformation Nucleic Acid Denaturation nucleocapsid protein Poly A Proviruses - genetics RNA, Spliced Leader - chemistry RNA, Spliced Leader - genetics RNA, Viral - chemistry RNA, Viral - genetics Sequence Deletion Thermodynamics |
title | Two alternating structures of the HIV-1 leader RNA |
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