DVOŘÁKOVÁ, Zuzana, Daniel RENČIUK, Iva KEJNOVSKÁ, Petra ŠKOLÁKOVÁ, Klára BEDNÁŘOVÁ, J SAGI and Michaela VORLÍČKOVÁ. i-Motif of cytosine-rich human telomere DNA fragments containing natural base lesions. Nucleic Acids Research. Oxford: Oxford University Press, 2018, vol. 46, No 4, p. 1624-1634. ISSN 0305-1048. Available from: https://dx.doi.org/10.1093/nar/gky035.
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Basic information
Original name i-Motif of cytosine-rich human telomere DNA fragments containing natural base lesions
Authors DVOŘÁKOVÁ, Zuzana, Daniel RENČIUK, Iva KEJNOVSKÁ, Petra ŠKOLÁKOVÁ, Klára BEDNÁŘOVÁ, J SAGI and Michaela VORLÍČKOVÁ.
Edition Nucleic Acids Research, Oxford, Oxford University Press, 2018, 0305-1048.
Other information
Original language English
Type of outcome Article in a journal
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 11.147
Doi http://dx.doi.org/10.1093/nar/gky035
UT WoS 000426293300012
Changed by Changed by: Mgr. Zuzana Dvořáková, Ph.D., učo 211080. Changed: 9/4/2018 15:13.
Abstract
i-Motif (iM) is a four stranded DNA structure formed by cytosine-rich sequences, which are often present in functionally important parts of the genome such as promoters of genes and telomeres. Using electronic circular dichroism and UV absorption spectroscopies and electrophoretic methods, we examined the effect of four naturally occurring DNA base lesions on the folding and stability of the iM formed by the human telomere DNA sequence (C3TAA) 3C3T. The results demonstrate that the TAA loop lesions, the apurinic site and 8-oxoadenine substituting for adenine, and the 5-hydroxymethyluracil substituting for thymine only marginally disturb the formation of iM. The presence of uracil, which is formed by enzymatic or spontaneous deamination of cytosine, shifts iM formation towards substantially more acidic pH values and simultaneously distinctly reduces iM stability. This effect depends on the position of the damage sites in the sequence. The results have enabled us to formulate additional rules for iM formation.
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