SN- and NS-puckered sugar conformers are precursors of the (6-4) photoproduct in thymine dinucleotide.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
16 03 2022
Historique:
pubmed: 8 3 2022
medline: 24 3 2022
entrez: 7 3 2022
Statut: epublish

Résumé

Some amount of furanose in a southern conformation, possibly in both, but certainly in one of the two adjacent nucleotides of a dipyrimidine site, is necessary for (6-4) photoproduct formation in oligonucleotides. To explore the necessity, role, and most favorable location of each South sugar conformer in the formation of the (6-4) adduct in the thymine dinucleotide TpT, the photochemical behavior of two synthetic analogues, in which the South sugar conformation is prohibited for one of their two sugars, has been examined. Herein, we experimentally demonstrate that the presence of one sugar presenting some amount of South puckering, at any of the extremities, is sufficient to trigger (6-4) adduct formation. Nonetheless, the photochemical behavior of the dinucleotide with a South-puckered conformation at the 5'-end, mimics more closely that of TpT. In addition, using the 5' North 3' South-dilocked dinucleotide, we demonstrate that the flexibility of the South pucker at the 3'-end has little influence on the (6-4) adduct formation.

Identifiants

pubmed: 35253821
doi: 10.1039/d2ob00044j
doi:

Substances chimiques

Thymine QR26YLT7LT

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2300-2307

Auteurs

Jouda Jakhlal (J)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR de Pharmacie, 51100 Reims, France. pascale.clivio@univ-reims.fr.

Clément Denhez (C)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR de Pharmacie, 51100 Reims, France. pascale.clivio@univ-reims.fr.
MaSCA, P3M, UFR des Sciences Exactes et Naturelles, 51100 Reims, France.

Stéphanie Coantic-Castex (S)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR de Pharmacie, 51100 Reims, France. pascale.clivio@univ-reims.fr.

Agathe Martinez (A)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR des Sciences Exactes et Naturelles, 51100 Reims, France.

Dominique Harakat (D)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR des Sciences Exactes et Naturelles, 51100 Reims, France.

Thierry Douki (T)

Université Grenoble Alpes, CEA, CNRS, IRIG, SyMMES, 38000 Grenoble, France.

Dominique Guillaume (D)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR de Pharmacie, 51100 Reims, France. pascale.clivio@univ-reims.fr.

Pascale Clivio (P)

Université de Reims Champagne Ardenne, Institut de Chimie Moléculaire de Reims, CNRS UMR 7312, UFR de Pharmacie, 51100 Reims, France. pascale.clivio@univ-reims.fr.

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Classifications MeSH