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Backbone-base inclination as a fundamental determinant of nucleic acid self- and cross-pairing

Identifieur interne : 000551 ( Ncbi/Merge ); précédent : 000550; suivant : 000552

Backbone-base inclination as a fundamental determinant of nucleic acid self- and cross-pairing

Auteurs : Pradeep S. Pallan [États-Unis] ; Paolo Lubini ; Martin Bolli [Suisse] ; Martin Egli [États-Unis]

Source :

RBID : PMC:2095819

Descripteurs français

English descriptors

Abstract

The crystal structure of the duplex formed by oligo(2′,3′-dideoxy-β-d-glucopyranosyl)nucleotides (homo-DNA) revealed strongly inclined backbone and base-pair axes [Egli,M., Pallan,P.S., Pattanayek,R., Wilds,C.J., Lubini,P., Minasov,G., Dobler,M., Leumann,C.J. and Eschenmoser,A. (2006) Crystal structure of homo-DNA and nature's choice of pentose over hexose in the genetic system. J. Am. Chem. Soc., 128, 10847–10856]. This inclination is easily perceived because homo-DNA exhibits only a modest helical twist. Conversely, the tight coiling of strands conceals that the backbone-base inclinations for A- (DNA and RNA) and B-form (DNA) duplexes differ considerably. We have defined a parameter ηB that corresponds to the local inclination between sugar-phosphate backbone and base plane in nucleic acid strands. Here, we show its biological significance as a predictive measure for the relative strand polarities (antiparallel, aps, or parallel, ps) in duplexes of DNA, RNA and artificial nucleic acid pairing systems. The potential of formation of ps duplexes between complementary 16-mers with eight A and U(T) residues each was investigated with DNA, RNA, 2′-O-methylated RNA, homo-DNA and p-RNA, the ribopyranosyl isomer of RNA. The thermodynamic stabilities of the corresponding aps duplexes were also measured. As shown previously, DNA is capable of forming both ps and aps duplexes. However, all other tested systems are unable to form stable ps duplexes with reverse Watson–Crick (rWC) base pairs. This observation illustrates the handicap encountered by nucleic acid systems with inclinations ηB that differ significantly from 0° to form a ps rWC paired duplex. Accordingly, RNA with a backbone-base inclination of −30°, pairs strictly in an aps fashion. On the other hand, the more or less perpendicular orientation of backbone and bases in DNA allows it to adopt a ps rWC paired duplex. In addition to providing a rationalization of relative strand polarity with nucleic acids, the backbone-base inclination parameter is also a determinant of cross-pairing. Thus, systems with strongly deviating ηB angles will not pair with each other. Nucleic acid pairing systems with significant backbone-base inclinations can also be expected to display different stabilities depending on which terminus carries unpaired nucleotides. The negative inclination of RNA is consistent with the higher stability of duplexes with 3′- compared to those with 5′-dangling ends.


Url:
DOI: 10.1093/nar/gkm612
PubMed: 17905816
PubMed Central: 2095819

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PMC:2095819

Le document en format XML

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<p>The crystal structure of the duplex formed by oligo(2′,3′-dideoxy-
<italic>β</italic>
-
<sc>d</sc>
-glucopyranosyl)nucleotides (homo-DNA) revealed strongly inclined backbone and base-pair axes [Egli,M., Pallan,P.S., Pattanayek,R., Wilds,C.J., Lubini,P., Minasov,G., Dobler,M., Leumann,C.J. and Eschenmoser,A. (2006) Crystal structure of homo-DNA and nature's choice of pentose over hexose in the genetic system.
<italic>J. Am. Chem. Soc</italic>
., 128, 10847–10856]. This inclination is easily perceived because homo-DNA exhibits only a modest helical twist. Conversely, the tight coiling of strands conceals that the backbone-base inclinations for A- (DNA and RNA) and B-form (DNA) duplexes differ considerably. We have defined a parameter
<italic>η</italic>
<sub>B</sub>
that corresponds to the local inclination between sugar-phosphate backbone and base plane in nucleic acid strands. Here, we show its biological significance as a predictive measure for the relative strand polarities (antiparallel,
<italic>aps</italic>
, or parallel,
<italic>ps</italic>
) in duplexes of DNA, RNA and artificial nucleic acid pairing systems. The potential of formation of
<italic>ps</italic>
duplexes between complementary 16-mers with eight A and U(T) residues each was investigated with DNA, RNA, 2′-
<italic>O</italic>
-methylated RNA, homo-DNA and p-RNA, the ribo
<italic>pyranosyl</italic>
isomer of RNA. The thermodynamic stabilities of the corresponding
<italic>aps</italic>
duplexes were also measured. As shown previously, DNA is capable of forming both
<italic>ps</italic>
and
<italic>aps</italic>
duplexes. However, all other tested systems are unable to form stable
<italic>ps</italic>
duplexes with reverse Watson–Crick (rWC) base pairs. This observation illustrates the handicap encountered by nucleic acid systems with inclinations η
<sub>B</sub>
that differ significantly from 0° to form a
<italic>ps</italic>
rWC paired duplex. Accordingly, RNA with a backbone-base inclination of −30
<bold>°</bold>
, pairs strictly in an
<italic>aps</italic>
fashion. On the other hand, the more or less perpendicular orientation of backbone and bases in DNA allows it to adopt a
<italic>ps</italic>
rWC paired duplex. In addition to providing a rationalization of relative strand polarity with nucleic acids, the backbone-base inclination parameter is also a determinant of cross-pairing. Thus, systems with strongly deviating
<italic>η</italic>
<sub>B</sub>
angles will not pair with each other. Nucleic acid pairing systems with significant backbone-base inclinations can also be expected to display different stabilities depending on which terminus carries unpaired nucleotides. The negative inclination of RNA is consistent with the higher stability of duplexes with 3′- compared to those with 5′-dangling ends.</p>
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</back>
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<titleStmt>
<title xml:lang="en">Backbone-base inclination as a fundamental determinant of nucleic acid self- and cross-pairing</title>
<author>
<name sortKey="Pallan, Pradeep S" sort="Pallan, Pradeep S" uniqKey="Pallan P" first="Pradeep S." last="Pallan">Pradeep S. Pallan</name>
<affiliation wicri:level="2">
<nlm:aff id="AFF1">Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA,</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lubini, Paolo" sort="Lubini, Paolo" uniqKey="Lubini P" first="Paolo" last="Lubini">Paolo Lubini</name>
<affiliation>
<nlm:aff wicri:cut=" and" id="AFF1">Alta Scuola Pedagogica, CH-6600 Locarno</nlm:aff>
<wicri:noCountry code="subfield">CH-6600 Locarno</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Bolli, Martin" sort="Bolli, Martin" uniqKey="Bolli M" first="Martin" last="Bolli">Martin Bolli</name>
<affiliation wicri:level="1">
<nlm:aff id="AFF1">Actelion Pharmaceuticals Ltd., CH-4123 Allschwil, Switzerland</nlm:aff>
<country xml:lang="fr">Suisse</country>
<wicri:regionArea>Actelion Pharmaceuticals Ltd., CH-4123 Allschwil</wicri:regionArea>
<wicri:noRegion>CH-4123 Allschwil</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Egli, Martin" sort="Egli, Martin" uniqKey="Egli M" first="Martin" last="Egli">Martin Egli</name>
<affiliation wicri:level="2">
<nlm:aff id="AFF1">Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA,</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
</placeName>
</affiliation>
</author>
</titleStmt>
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<idno type="wicri:source">PMC</idno>
<idno type="pmid">17905816</idno>
<idno type="pmc">2095819</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2095819</idno>
<idno type="RBID">PMC:2095819</idno>
<idno type="doi">10.1093/nar/gkm612</idno>
<date when="2007">2007</date>
<idno type="wicri:Area/Pmc/Corpus">000F41</idno>
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<idno type="wicri:Area/Pmc/Checkpoint">001417</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">001417</idno>
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<analytic>
<title xml:lang="en" level="a" type="main">Backbone-base inclination as a fundamental determinant of nucleic acid self- and cross-pairing</title>
<author>
<name sortKey="Pallan, Pradeep S" sort="Pallan, Pradeep S" uniqKey="Pallan P" first="Pradeep S." last="Pallan">Pradeep S. Pallan</name>
<affiliation wicri:level="2">
<nlm:aff id="AFF1">Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA,</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lubini, Paolo" sort="Lubini, Paolo" uniqKey="Lubini P" first="Paolo" last="Lubini">Paolo Lubini</name>
<affiliation>
<nlm:aff wicri:cut=" and" id="AFF1">Alta Scuola Pedagogica, CH-6600 Locarno</nlm:aff>
<wicri:noCountry code="subfield">CH-6600 Locarno</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Bolli, Martin" sort="Bolli, Martin" uniqKey="Bolli M" first="Martin" last="Bolli">Martin Bolli</name>
<affiliation wicri:level="1">
<nlm:aff id="AFF1">Actelion Pharmaceuticals Ltd., CH-4123 Allschwil, Switzerland</nlm:aff>
<country xml:lang="fr">Suisse</country>
<wicri:regionArea>Actelion Pharmaceuticals Ltd., CH-4123 Allschwil</wicri:regionArea>
<wicri:noRegion>CH-4123 Allschwil</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Egli, Martin" sort="Egli, Martin" uniqKey="Egli M" first="Martin" last="Egli">Martin Egli</name>
<affiliation wicri:level="2">
<nlm:aff id="AFF1">Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA,</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
</placeName>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Nucleic Acids Research</title>
<idno type="ISSN">0305-1048</idno>
<idno type="eISSN">1362-4962</idno>
<imprint>
<date when="2007">2007</date>
</imprint>
</series>
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<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>The crystal structure of the duplex formed by oligo(2′,3′-dideoxy-
<italic>β</italic>
-
<sc>d</sc>
-glucopyranosyl)nucleotides (homo-DNA) revealed strongly inclined backbone and base-pair axes [Egli,M., Pallan,P.S., Pattanayek,R., Wilds,C.J., Lubini,P., Minasov,G., Dobler,M., Leumann,C.J. and Eschenmoser,A. (2006) Crystal structure of homo-DNA and nature's choice of pentose over hexose in the genetic system.
<italic>J. Am. Chem. Soc</italic>
., 128, 10847–10856]. This inclination is easily perceived because homo-DNA exhibits only a modest helical twist. Conversely, the tight coiling of strands conceals that the backbone-base inclinations for A- (DNA and RNA) and B-form (DNA) duplexes differ considerably. We have defined a parameter
<italic>η</italic>
<sub>B</sub>
that corresponds to the local inclination between sugar-phosphate backbone and base plane in nucleic acid strands. Here, we show its biological significance as a predictive measure for the relative strand polarities (antiparallel,
<italic>aps</italic>
, or parallel,
<italic>ps</italic>
) in duplexes of DNA, RNA and artificial nucleic acid pairing systems. The potential of formation of
<italic>ps</italic>
duplexes between complementary 16-mers with eight A and U(T) residues each was investigated with DNA, RNA, 2′-
<italic>O</italic>
-methylated RNA, homo-DNA and p-RNA, the ribo
<italic>pyranosyl</italic>
isomer of RNA. The thermodynamic stabilities of the corresponding
<italic>aps</italic>
duplexes were also measured. As shown previously, DNA is capable of forming both
<italic>ps</italic>
and
<italic>aps</italic>
duplexes. However, all other tested systems are unable to form stable
<italic>ps</italic>
duplexes with reverse Watson–Crick (rWC) base pairs. This observation illustrates the handicap encountered by nucleic acid systems with inclinations η
<sub>B</sub>
that differ significantly from 0° to form a
<italic>ps</italic>
rWC paired duplex. Accordingly, RNA with a backbone-base inclination of −30
<bold>°</bold>
, pairs strictly in an
<italic>aps</italic>
fashion. On the other hand, the more or less perpendicular orientation of backbone and bases in DNA allows it to adopt a
<italic>ps</italic>
rWC paired duplex. In addition to providing a rationalization of relative strand polarity with nucleic acids, the backbone-base inclination parameter is also a determinant of cross-pairing. Thus, systems with strongly deviating
<italic>η</italic>
<sub>B</sub>
angles will not pair with each other. Nucleic acid pairing systems with significant backbone-base inclinations can also be expected to display different stabilities depending on which terminus carries unpaired nucleotides. The negative inclination of RNA is consistent with the higher stability of duplexes with 3′- compared to those with 5′-dangling ends.</p>
</div>
</front>
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<name sortKey="Bolli, Martin" sort="Bolli, Martin" uniqKey="Bolli M" first="Martin" last="Bolli">Martin Bolli</name>
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<author>
<name sortKey="Egli, Martin" sort="Egli, Martin" uniqKey="Egli M" first="Martin" last="Egli">Martin Egli</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2007">2007</date>
<idno type="RBID">pubmed:17905816</idno>
<idno type="pmid">17905816</idno>
<idno type="doi">10.1093/nar/gkm612</idno>
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<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">002075</idno>
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<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Backbone-base inclination as a fundamental determinant of nucleic acid self- and cross-pairing.</title>
<author>
<name sortKey="Pallan, Pradeep S" sort="Pallan, Pradeep S" uniqKey="Pallan P" first="Pradeep S" last="Pallan">Pradeep S. Pallan</name>
<affiliation wicri:level="2">
<nlm:affiliation>Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biochemistry, School of Medicine, Vanderbilt University, Nashville, TN 37232</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lubini, Paolo" sort="Lubini, Paolo" uniqKey="Lubini P" first="Paolo" last="Lubini">Paolo Lubini</name>
</author>
<author>
<name sortKey="Bolli, Martin" sort="Bolli, Martin" uniqKey="Bolli M" first="Martin" last="Bolli">Martin Bolli</name>
</author>
<author>
<name sortKey="Egli, Martin" sort="Egli, Martin" uniqKey="Egli M" first="Martin" last="Egli">Martin Egli</name>
</author>
</analytic>
<series>
<title level="j">Nucleic acids research</title>
<idno type="eISSN">1362-4962</idno>
<imprint>
<date when="2007" type="published">2007</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Base Pairing</term>
<term>DNA (chemistry)</term>
<term>Models, Molecular</term>
<term>Peptide Nucleic Acids (chemistry)</term>
<term>RNA (chemistry)</term>
<term>Thermodynamics</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ADN ()</term>
<term>ARN ()</term>
<term>Acides nucléiques peptidiques ()</term>
<term>Appariement de bases</term>
<term>Modèles moléculaires</term>
<term>Thermodynamique</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>DNA</term>
<term>Peptide Nucleic Acids</term>
<term>RNA</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Base Pairing</term>
<term>Models, Molecular</term>
<term>Thermodynamics</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>ADN</term>
<term>ARN</term>
<term>Acides nucléiques peptidiques</term>
<term>Appariement de bases</term>
<term>Modèles moléculaires</term>
<term>Thermodynamique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">The crystal structure of the duplex formed by oligo(2',3'-dideoxy-beta-d-glucopyranosyl)nucleotides (homo-DNA) revealed strongly inclined backbone and base-pair axes [Egli,M., Pallan,P.S., Pattanayek,R., Wilds,C.J., Lubini,P., Minasov,G., Dobler,M., Leumann,C.J. and Eschenmoser,A. (2006) Crystal structure of homo-DNA and nature's choice of pentose over hexose in the genetic system. J. Am. Chem. Soc., 128, 10847-10856]. This inclination is easily perceived because homo-DNA exhibits only a modest helical twist. Conversely, the tight coiling of strands conceals that the backbone-base inclinations for A- (DNA and RNA) and B-form (DNA) duplexes differ considerably. We have defined a parameter eta(B) that corresponds to the local inclination between sugar-phosphate backbone and base plane in nucleic acid strands. Here, we show its biological significance as a predictive measure for the relative strand polarities (antiparallel, aps, or parallel, ps) in duplexes of DNA, RNA and artificial nucleic acid pairing systems. The potential of formation of ps duplexes between complementary 16-mers with eight A and U(T) residues each was investigated with DNA, RNA, 2'-O-methylated RNA, homo-DNA and p-RNA, the ribopyranosyl isomer of RNA. The thermodynamic stabilities of the corresponding aps duplexes were also measured. As shown previously, DNA is capable of forming both ps and aps duplexes. However, all other tested systems are unable to form stable ps duplexes with reverse Watson-Crick (rWC) base pairs. This observation illustrates the handicap encountered by nucleic acid systems with inclinations eta(B) that differ significantly from 0 degrees to form a ps rWC paired duplex. Accordingly, RNA with a backbone-base inclination of -30 degrees , pairs strictly in an aps fashion. On the other hand, the more or less perpendicular orientation of backbone and bases in DNA allows it to adopt a ps rWC paired duplex. In addition to providing a rationalization of relative strand polarity with nucleic acids, the backbone-base inclination parameter is also a determinant of cross-pairing. Thus, systems with strongly deviating eta(B) angles will not pair with each other. Nucleic acid pairing systems with significant backbone-base inclinations can also be expected to display different stabilities depending on which terminus carries unpaired nucleotides. The negative inclination of RNA is consistent with the higher stability of duplexes with 3'- compared to those with 5'-dangling ends.</div>
</front>
</TEI>
</pubmed>
</double>
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