4.7 Article

Experimental approaches to identify cellular G-quadruplex structures and functions

Journal

METHODS
Volume 57, Issue 1, Pages 84-92

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2012.01.008

Keywords

G-quadruplex; Genomic mapping; Pull-down; Cross-linking; Chromatin immuno-precipitation (ChIP); Cellular imaging; Quinone methides; DNA damage response; Unbiased approaches; Sequencing

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/G008337/1] Funding Source: Medline
  2. Cancer Research UK [11961] Funding Source: Medline
  3. BBSRC [BB/G008337/1] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/G008337/1] Funding Source: researchfish
  5. Cancer Research UK [11961] Funding Source: researchfish

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Guanine-rich nucleic acids can fold into non-canonical DNA secondary structures called G-quadruplexes. The formation of these structures can interfere with the biology that is crucial to sustain cellular homeostases and metabolism via mechanisms that include transcription, translation, splicing, telomere maintenance and DNA recombination. Thus, due to their implication in several biological processes and possible role promoting genomic instability, G-quadruplex forming sequences have emerged as potential therapeutic targets. There has been a growing interest in the development of synthetic molecules and biomolecules for sensing G-quadruplex structures in cellular DNA. In this review, we summarise and discuss recent methods developed for cellular imaging of G-quadruplexes, and the application of experimental genomic approaches to detect G-quadruplexes throughout genomic DNA. In particular, we will discuss the use of engineered small molecules and natural proteins to enable pull-down, ChIP-Seq. ChIP-chip and fluorescence imaging of G-quadruplex structures in cellular DNA. (C) 2012 Elsevier Inc. All rights reserved.

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