Non-B DNA structure-induced genetic instability and evolution
Top Cited Papers
- 1 September 2009
- journal article
- review article
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 67 (1) , 43-62
- https://doi.org/10.1007/s00018-009-0131-2
Abstract
Repetitive DNA motifs are abundant in the genomes of various species and have the capacity to adopt non-canonical (i.e., non-B) DNA structures. Several non-B DNA structures, including cruciforms, slipped structures, triplexes, G-quadruplexes, and Z-DNA, have been shown to cause mutations, such as deletions, expansions, and translocations in both prokaryotes and eukaryotes. Their distributions in genomes are not random and often co-localize with sites of chromosomal breakage associated with genetic diseases. Current genome-wide sequence analyses suggest that the genomic instabilities induced by non-B DNA structure-forming sequences not only result in predisposition to disease, but also contribute to rapid evolutionary changes, particularly in genes associated with development and regulatory functions. In this review, we describe the occurrence of non-B DNA-forming sequences in various species, the classes of genes enriched in non-B DNA-forming sequences, and recent mechanistic studies on DNA structure-induced genomic instability to highlight their importance in genomes.Keywords
This publication has 170 references indexed in Scilit:
- Methods to determine DNA structural alterations and genetic instabilityPublished by Elsevier ,2009
- Models for chromosomal replication‐independent non‐B DNA structure‐induced genetic instabilityMolecular Carcinogenesis, 2009
- Large inverted repeats in the vicinity of a single double-strand break strongly affect repair in yeast diploids lacking Rad51Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 2008
- Structures, folding patterns, and functions of intramolecular DNA G-quadruplexes found in eukaryotic promoter regionsBiochimie, 2008
- DNA triple helices: Biological consequences and therapeutic potentialPublished by Elsevier ,2008
- Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangementsDevelopmental Disabilities Research Reviews, 2008
- An AT-Rich Sequence in Human Common Fragile Site FRA16D Causes Fork Stalling and Chromosome Breakage in S. cerevisiaeMolecular Cell, 2007
- Palindrome-mediated chromosomal translocations in humansDNA Repair, 2006
- A sodium-potassium switch in the formation of four-stranded G4-DNANature, 1990
- Formation of parallel four-stranded complexes by guanine-rich motifs in DNA and its implications for meiosisNature, 1988