Clustered abasic lesions profoundly change the structure and stability of human telomeric G-quadruplexes
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28369584
PubMed Central
PMC5416849
DOI
10.1093/nar/gkx191
PII: 3078563
Knihovny.cz E-zdroje
- MeSH
- adenin chemie MeSH
- cirkulární dichroismus MeSH
- DNA chemie genetika MeSH
- furany chemie MeSH
- G-kvadruplexy * MeSH
- lidé MeSH
- molekulární modely MeSH
- nukleární magnetická rezonance biomolekulární MeSH
- oligonukleotidy chemie MeSH
- roztoky MeSH
- telomery genetika ultrastruktura MeSH
- zkracování telomer * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenin MeSH
- DNA MeSH
- furany MeSH
- oligonukleotidy MeSH
- roztoky MeSH
Ionizing radiation produces clustered damage to DNA which is difficult to repair and thus more harmful than single lesions. Clustered lesions have only been investigated in dsDNA models. Introducing the term 'clustered damage to G-quadruplexes' we report here on the structural effects of multiple tetrahydrofuranyl abasic sites replacing loop adenines (A/AP) and tetrad guanines (G/AP) in quadruplexes formed by the human telomere d[AG3(TTAG3)3] (htel-22) and d[TAG3(TTAG3)3TT] (htel-25) in K+ solutions. Single to triple A/APs increased the population of parallel strands in their structures by stabilizing propeller type loops, shifting the antiparallel htel-22 into hybrid or parallel quadruplexes. In htel-25, the G/APs inhibited the formation of parallel strands and these adopted antiparallel topologies. Clustered G/AP and A/APs reduced the thermal stability of the wild-type htel-25. Depending on position, A/APs diminished or intensified the damaging effect of the G/APs. Taken together, clustered lesions can disrupt the topology and stability of the htel quadruplexes and restrict their conformational space. These in vitro results suggest that formation of clustered lesions in the chromosome capping structure can result in the unfolding of existing G-quadruplexes which can lead to telomere shortening.
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