Different intrastrand and interstrand contributions to stacking account for roll variations at the alternating purine-pyrimidine sequences in A-DNA and A-RNA
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články
PubMed
1719210
DOI
10.1016/0022-2836(91)80172-q
PII: 0022-2836(91)80172-Q
Knihovny.cz E-zdroje
- MeSH
- DNA chemie MeSH
- konformace nukleové kyseliny MeSH
- molekulární sekvence - údaje MeSH
- RNA chemie MeSH
- sekvence nukleotidů MeSH
- termodynamika MeSH
- zastoupení bazí MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- DNA MeSH
- RNA MeSH
An explanation is suggested for the roll alternation between low and high values in A-type nucleic acid duplexes containing alternating sequences of purine and pyrimidine residues. The explanation combines two points. (1) Roll inevitably occurs in A-type duplexes due to geometrical reasons. (2) Intrastrand base stacking is much more impaired by roll than interstrand base stacking in A-type duplexes. Therefore purine-pyrimidine steps, whose bases mainly exhibit an intrastrand stacking, resist roll and decrease it. By contrast, bases at pyrimidine-purine steps exhibit a significant interstrand stacking that is tolerant to roll in A-type nucleic acid duplexes. In consequence, it is favourable if the purine-pyrimidine and pyrimidine-purine steps adopt low and high rolls, respectively in A-conformations of DNA and RNA molecules containing alternating purine-pyrimidine sequences. This is actually observed in the relevant molecular crystal structures.
Citace poskytuje Crossref.org
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