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Thermodynamic examination of trinucleotide bulged RNA in the context of HIV-1 TAR RNA
RNA structures contain many bulges and loops that are expected to be sites for inter- and intra-molecular interactions. Nucleotides in the bulge are expected to influence the structure and recognition of RNA. The same stability is assigned to all trinucleotide bulged RNA in the current secondary str...
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Published in: | RNA (Cambridge) 2008-12, Vol.14 (12), p.2550-2556 |
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creator | Carter-O'Connell, Ian Booth, David Eason, Bryan Grover, Neena |
description | RNA structures contain many bulges and loops that are expected to be sites for inter- and intra-molecular interactions. Nucleotides in the bulge are expected to influence the structure and recognition of RNA. The same stability is assigned to all trinucleotide bulged RNA in the current secondary structure prediction models. In this study thermal denaturation experiments were performed on four trinucleotide bulged RNA, in the context of HIV-1 TAR RNA, to determine whether the bulge sequence affects RNA stability and its divalent ion interactions. Cytosine-rich bulged RNA were more stable than uracil-rich bulged RNA in 1 M KCl. Interactions of divalent ions were more favorable with uracil-rich bulged RNA by approximately 2 kcal/mol over cytosine-rich bulged RNA. The UCU-TAR RNA (wild type) is stabilized by 1.7 kcal/mol in 9.5 mM Ca(2+) as compared with 1 M KCl, whereas no additional gain in stability is measured for CCC-TAR RNA. These results have implications for base substitution experiments traditionally employed to identify metal ion binding sites. To our knowledge, this is the first systematic study to quantify the effect of small sequence changes on RNA stability upon interactions with divalent ions. |
doi_str_mv | 10.1261/rna.1004108 |
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Nucleotides in the bulge are expected to influence the structure and recognition of RNA. The same stability is assigned to all trinucleotide bulged RNA in the current secondary structure prediction models. In this study thermal denaturation experiments were performed on four trinucleotide bulged RNA, in the context of HIV-1 TAR RNA, to determine whether the bulge sequence affects RNA stability and its divalent ion interactions. Cytosine-rich bulged RNA were more stable than uracil-rich bulged RNA in 1 M KCl. Interactions of divalent ions were more favorable with uracil-rich bulged RNA by approximately 2 kcal/mol over cytosine-rich bulged RNA. The UCU-TAR RNA (wild type) is stabilized by 1.7 kcal/mol in 9.5 mM Ca(2+) as compared with 1 M KCl, whereas no additional gain in stability is measured for CCC-TAR RNA. These results have implications for base substitution experiments traditionally employed to identify metal ion binding sites. 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Nucleotides in the bulge are expected to influence the structure and recognition of RNA. The same stability is assigned to all trinucleotide bulged RNA in the current secondary structure prediction models. In this study thermal denaturation experiments were performed on four trinucleotide bulged RNA, in the context of HIV-1 TAR RNA, to determine whether the bulge sequence affects RNA stability and its divalent ion interactions. Cytosine-rich bulged RNA were more stable than uracil-rich bulged RNA in 1 M KCl. Interactions of divalent ions were more favorable with uracil-rich bulged RNA by approximately 2 kcal/mol over cytosine-rich bulged RNA. The UCU-TAR RNA (wild type) is stabilized by 1.7 kcal/mol in 9.5 mM Ca(2+) as compared with 1 M KCl, whereas no additional gain in stability is measured for CCC-TAR RNA. These results have implications for base substitution experiments traditionally employed to identify metal ion binding sites. To our knowledge, this is the first systematic study to quantify the effect of small sequence changes on RNA stability upon interactions with divalent ions.</description><subject>Base Sequence</subject><subject>HIV-1 - chemistry</subject><subject>Nucleic Acid Conformation</subject><subject>Potassium Chloride - metabolism</subject><subject>RNA Stability</subject><subject>RNA, Viral - chemistry</subject><subject>RNA, Viral - metabolism</subject><subject>Thermodynamics</subject><issn>1355-8382</issn><issn>1469-9001</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNpVkUlLBDEQhYMo7ifvkpMXac3SSToXYRA3EAUZvYZMp8aJdCeaTov-ezM4uJyqqPfxqqiH0AElJ5RJepqCPaGE1JQ0a2ib1lJXmhC6XnouRNXwhm2hnWF4KUNe5E20RRstWMPoNnqcLiD10X0G2_sWw0cpwWYfA45znJMPY9tBzN4Bno3dMzj8cDfBPuC8ANzGkOEjL9Hrm6eK4unkYanvoY257QbYX9Vd9Hh5MT2_rm7vr27OJ7dVy5XOlROikUQyZlupaM2dstKCdRyY1Eq4WjVaK6drRVU9q4FRPmOKOickCEIY30Vn376v46wH10LIyXbmNfnepk8TrTf_leAX5jm-GyY00ZIWg6OVQYpvIwzZ9H5ooetsgDgORuqmXKLrAh5_g22Kw5Bg_rOEErOMwZQYzCqGQh_-veuXXf2dfwHG3oJG</recordid><startdate>200812</startdate><enddate>200812</enddate><creator>Carter-O'Connell, Ian</creator><creator>Booth, David</creator><creator>Eason, Bryan</creator><creator>Grover, Neena</creator><general>Cold Spring Harbor Laboratory 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>7X8</scope><scope>5PM</scope></search><sort><creationdate>200812</creationdate><title>Thermodynamic examination of trinucleotide bulged RNA in the context of HIV-1 TAR RNA</title><author>Carter-O'Connell, Ian ; Booth, David ; Eason, Bryan ; Grover, Neena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-d55860622ac67143d7a6aead3e26975d478997d947174b4e213b271dd56e50023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Base Sequence</topic><topic>HIV-1 - chemistry</topic><topic>Nucleic Acid Conformation</topic><topic>Potassium Chloride - metabolism</topic><topic>RNA Stability</topic><topic>RNA, Viral - chemistry</topic><topic>RNA, Viral - metabolism</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carter-O'Connell, Ian</creatorcontrib><creatorcontrib>Booth, David</creatorcontrib><creatorcontrib>Eason, Bryan</creatorcontrib><creatorcontrib>Grover, Neena</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>RNA (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carter-O'Connell, Ian</au><au>Booth, David</au><au>Eason, Bryan</au><au>Grover, Neena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermodynamic examination of trinucleotide bulged RNA in the context of HIV-1 TAR RNA</atitle><jtitle>RNA (Cambridge)</jtitle><addtitle>RNA</addtitle><date>2008-12</date><risdate>2008</risdate><volume>14</volume><issue>12</issue><spage>2550</spage><epage>2556</epage><pages>2550-2556</pages><issn>1355-8382</issn><eissn>1469-9001</eissn><abstract>RNA structures contain many bulges and loops that are expected to be sites for inter- and intra-molecular interactions. Nucleotides in the bulge are expected to influence the structure and recognition of RNA. The same stability is assigned to all trinucleotide bulged RNA in the current secondary structure prediction models. In this study thermal denaturation experiments were performed on four trinucleotide bulged RNA, in the context of HIV-1 TAR RNA, to determine whether the bulge sequence affects RNA stability and its divalent ion interactions. Cytosine-rich bulged RNA were more stable than uracil-rich bulged RNA in 1 M KCl. Interactions of divalent ions were more favorable with uracil-rich bulged RNA by approximately 2 kcal/mol over cytosine-rich bulged RNA. The UCU-TAR RNA (wild type) is stabilized by 1.7 kcal/mol in 9.5 mM Ca(2+) as compared with 1 M KCl, whereas no additional gain in stability is measured for CCC-TAR RNA. These results have implications for base substitution experiments traditionally employed to identify metal ion binding sites. To our knowledge, this is the first systematic study to quantify the effect of small sequence changes on RNA stability upon interactions with divalent ions.</abstract><cop>United States</cop><pub>Cold Spring Harbor Laboratory Press</pub><pmid>18952821</pmid><doi>10.1261/rna.1004108</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence HIV-1 - chemistry Nucleic Acid Conformation Potassium Chloride - metabolism RNA Stability RNA, Viral - chemistry RNA, Viral - metabolism Thermodynamics |
title | Thermodynamic examination of trinucleotide bulged RNA in the context of HIV-1 TAR RNA |
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