1lai

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(New page: 200px<br /><applet load="1lai" size="450" color="white" frame="true" align="right" spinBox="true" caption="1lai" /> '''Solution Structure of the B-DNA Duplex CGCGG...)
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'''Solution Structure of the B-DNA Duplex CGCGGTGTCCGCG.'''<br />
'''Solution Structure of the B-DNA Duplex CGCGGTGTCCGCG.'''<br />
==Overview==
==Overview==
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The structure of the 1,N(2)-Propanodeoxyguanosine (PdG) adduct was, determined at pH 5.2 in the oligodeoxynucleotide duplex, 5'-d(CGCGGTXTCCGCG)3'.5'-d(CGCGGACACCGCG)-3' (X = PdG). This sequence, referred to as the -TXT- sequence, is contained within the Salmonella, typhimurium hisD3052 gene and contains a palindrome, representing a, potential hotspot for frameshift mutagenesis. PdG provides a model for the, primary adduct induced in DNA by malondialdehyde, the, 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)pyrimido[1,2-a]-purin-10(3H)-one, (M(1)G) lesion. The solution structure was refined by molecular dynamics, calculations restrained by a combination of NMR-derived distances and, dihedral angles, using a simulated annealing protocol. PdG introduced a, localized perturbation into the sequence at base pair X(7).C(20), which, was pH-dependent. At neutral pH, conformational exchange resulted in, spectral line broadening, and it was not possible to determine the, structure. A stable structure was observed at pH 5.2 in which PdG rotated, about the glycosyl bond into the syn conformation. This placed the, exocyclic moiety into the major groove of the duplex. PdG formed a, protonated Hoogsteen pair with nucleotide C(20) in the complementary, strand. The pseudorotation of the deoxyribose at C(20) was altered to an, approximately equal blend of C2'-endo and C3'-endo structures. However, these made little difference in the overall structure of the modified, oligodeoxynucleotide. The structure was compared to that of PdG in the, 5'-d(CGCXCGGCATG)-3'.5'-(CATGCCGCGCG)-3' sequence (the -CXC- sequence) at, pH 5.8 [Singh, U. S., Moe, J. G., Reddy, G. R., Weisenseel, J. P., Marnett, L. J., and Stone, M. P. (1993) Chem. Res. Toxicol. 6, 825-836]. A, sequence effect was observed. When PdG was placed into the -TXT- sequence, at low pH, the structural perturbation was limited to the X(7).C(20) base, pair. In contrast, when PdG was placed into the -CXC- sequence at low pH, both the modified base pair and its 3'-neighbor base pair were disrupted., The results are discussed in the context of differential outcomes for, site-specific mutagenesis and replication bypass experiments when PdG was, placed in the -TXT- and -CXC- sequences, respectively.
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The structure of the 1,N(2)-Propanodeoxyguanosine (PdG) adduct was determined at pH 5.2 in the oligodeoxynucleotide duplex 5'-d(CGCGGTXTCCGCG)3'.5'-d(CGCGGACACCGCG)-3' (X = PdG). This sequence, referred to as the -TXT- sequence, is contained within the Salmonella typhimurium hisD3052 gene and contains a palindrome, representing a potential hotspot for frameshift mutagenesis. PdG provides a model for the primary adduct induced in DNA by malondialdehyde, the 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)pyrimido[1,2-a]-purin-10(3H)-one (M(1)G) lesion. The solution structure was refined by molecular dynamics calculations restrained by a combination of NMR-derived distances and dihedral angles, using a simulated annealing protocol. PdG introduced a localized perturbation into the sequence at base pair X(7).C(20), which was pH-dependent. At neutral pH, conformational exchange resulted in spectral line broadening, and it was not possible to determine the structure. A stable structure was observed at pH 5.2 in which PdG rotated about the glycosyl bond into the syn conformation. This placed the exocyclic moiety into the major groove of the duplex. PdG formed a protonated Hoogsteen pair with nucleotide C(20) in the complementary strand. The pseudorotation of the deoxyribose at C(20) was altered to an approximately equal blend of C2'-endo and C3'-endo structures. However, these made little difference in the overall structure of the modified oligodeoxynucleotide. The structure was compared to that of PdG in the 5'-d(CGCXCGGCATG)-3'.5'-(CATGCCGCGCG)-3' sequence (the -CXC- sequence) at pH 5.8 [Singh, U. S., Moe, J. G., Reddy, G. R., Weisenseel, J. P., Marnett, L. J., and Stone, M. P. (1993) Chem. Res. Toxicol. 6, 825-836]. A sequence effect was observed. When PdG was placed into the -TXT- sequence at low pH, the structural perturbation was limited to the X(7).C(20) base pair. In contrast, when PdG was placed into the -CXC- sequence at low pH, both the modified base pair and its 3'-neighbor base pair were disrupted. The results are discussed in the context of differential outcomes for site-specific mutagenesis and replication bypass experiments when PdG was placed in the -TXT- and -CXC- sequences, respectively.
==About this Structure==
==About this Structure==
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1LAI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1LAI OCA].
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1LAI is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1LAI OCA].
==Reference==
==Reference==
Structure of an oligodeoxynucleotide containing a 1,N(2)-propanodeoxyguanosine adduct positioned in a palindrome derived from the Salmonella typhimurium hisD3052 gene: Hoogsteen pairing at pH 5.2., Weisenseel JP, Reddy GR, Marnett LJ, Stone MP, Chem Res Toxicol. 2002 Feb;15(2):127-39. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11849038 11849038]
Structure of an oligodeoxynucleotide containing a 1,N(2)-propanodeoxyguanosine adduct positioned in a palindrome derived from the Salmonella typhimurium hisD3052 gene: Hoogsteen pairing at pH 5.2., Weisenseel JP, Reddy GR, Marnett LJ, Stone MP, Chem Res Toxicol. 2002 Feb;15(2):127-39. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11849038 11849038]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Marnett, L.J.]]
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[[Category: Marnett, L J.]]
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[[Category: Reddy, G.R.]]
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[[Category: Reddy, G R.]]
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[[Category: Stone, M.P.]]
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[[Category: Stone, M P.]]
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[[Category: Weisenseel, J.P.]]
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[[Category: Weisenseel, J P.]]
[[Category: b-type]]
[[Category: b-type]]
[[Category: dna]]
[[Category: dna]]
[[Category: nmr]]
[[Category: nmr]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:43:45 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:43:05 2008''

Revision as of 11:43, 21 February 2008


1lai

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Solution Structure of the B-DNA Duplex CGCGGTGTCCGCG.

Overview

The structure of the 1,N(2)-Propanodeoxyguanosine (PdG) adduct was determined at pH 5.2 in the oligodeoxynucleotide duplex 5'-d(CGCGGTXTCCGCG)3'.5'-d(CGCGGACACCGCG)-3' (X = PdG). This sequence, referred to as the -TXT- sequence, is contained within the Salmonella typhimurium hisD3052 gene and contains a palindrome, representing a potential hotspot for frameshift mutagenesis. PdG provides a model for the primary adduct induced in DNA by malondialdehyde, the 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)pyrimido[1,2-a]-purin-10(3H)-one (M(1)G) lesion. The solution structure was refined by molecular dynamics calculations restrained by a combination of NMR-derived distances and dihedral angles, using a simulated annealing protocol. PdG introduced a localized perturbation into the sequence at base pair X(7).C(20), which was pH-dependent. At neutral pH, conformational exchange resulted in spectral line broadening, and it was not possible to determine the structure. A stable structure was observed at pH 5.2 in which PdG rotated about the glycosyl bond into the syn conformation. This placed the exocyclic moiety into the major groove of the duplex. PdG formed a protonated Hoogsteen pair with nucleotide C(20) in the complementary strand. The pseudorotation of the deoxyribose at C(20) was altered to an approximately equal blend of C2'-endo and C3'-endo structures. However, these made little difference in the overall structure of the modified oligodeoxynucleotide. The structure was compared to that of PdG in the 5'-d(CGCXCGGCATG)-3'.5'-(CATGCCGCGCG)-3' sequence (the -CXC- sequence) at pH 5.8 [Singh, U. S., Moe, J. G., Reddy, G. R., Weisenseel, J. P., Marnett, L. J., and Stone, M. P. (1993) Chem. Res. Toxicol. 6, 825-836]. A sequence effect was observed. When PdG was placed into the -TXT- sequence at low pH, the structural perturbation was limited to the X(7).C(20) base pair. In contrast, when PdG was placed into the -CXC- sequence at low pH, both the modified base pair and its 3'-neighbor base pair were disrupted. The results are discussed in the context of differential outcomes for site-specific mutagenesis and replication bypass experiments when PdG was placed in the -TXT- and -CXC- sequences, respectively.

About this Structure

1LAI is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Structure of an oligodeoxynucleotide containing a 1,N(2)-propanodeoxyguanosine adduct positioned in a palindrome derived from the Salmonella typhimurium hisD3052 gene: Hoogsteen pairing at pH 5.2., Weisenseel JP, Reddy GR, Marnett LJ, Stone MP, Chem Res Toxicol. 2002 Feb;15(2):127-39. PMID:11849038

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