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Identification of multiple genomic DNA sequences which form i-motif structures at neutral pH. | LitMetric

Identification of multiple genomic DNA sequences which form i-motif structures at neutral pH.

Nucleic Acids Res

School of Pharmacy, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ, UK.

Published: April 2017

AI Article Synopsis

  • i-Motifs are alternative DNA structures that can form in cytosine-rich sequences, notably under near-physiological conditions, challenging the belief they were only stable in acidic environments.
  • A systematic study demonstrated that longer tracts of consecutive cytosines lead to increased thermal stability of these structures, with at least five cytosines allowing i-motif folding at room temperature and neutral pH.
  • The findings suggest that numerous cytosine-rich sequences in the human genome may fold into i-motifs, particularly in regions that could affect gene expression, with 17 specific stable examples identified.

Article Abstract

i-Motifs are alternative DNA secondary structures formed in cytosine-rich sequences. Particular examples of these structures, traditionally assumed to be stable only at acidic pH, have been found to form under near-physiological conditions. To determine the potential impact of these structures on physiological processes, investigation of sequences with the capacity to fold under physiological conditions is required. Here we describe a systematic study of cytosine-rich DNA sequences, with varying numbers of consecutive cytosines, to gain insights into i-motif DNA sequence and structure stability. i-Motif formation was assessed using ultraviolet spectroscopy, circular dichroism and native gel electrophoresis. We found that increasing cytosine tract lengths resulted in increased thermal stability; sequences with at least five cytosines per tract folded into i-motif at room temperature and neutral pH. Using these results, we postulated a folding rule for i-motif formation, analogous to (but different from) that for G-quadruplexes. This indicated that thousands of cytosine-rich sequences in the human genome may fold into i-motif structures under physiological conditions. Many of these were found in locations where structure formation is likely to influence gene expression. Characterization of a selection of these identified i-motif forming sequences uncovered 17 genomic i-motif forming sequence examples which were stable at neutral pH.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605235PMC
http://dx.doi.org/10.1093/nar/gkx090DOI Listing

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