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DNA fragility in the parallel evolution of pelvic reduction in stickleback fish.

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TLDR
It is shown that a pelvic enhancer gene lies within a region of the genome that is prone to double-stranded DNA breakage owing to a high thymine-guanine content, which could lead to enhanced mutation rates that facilitate repeated adaptations to new environments.
Abstract
Evolution generates a remarkable breadth of living forms, but many traits evolve repeatedly, by mechanisms that are still poorly understood. A classic example of repeated evolution is the loss of pelvic hindfins in stickleback fish (Gasterosteus aculeatus). Repeated pelvic loss maps to recurrent deletions of a pelvic enhancer of the Pitx1 gene. Here, we identify molecular features contributing to these recurrent deletions. Pitx1 enhancer sequences form alternative DNA structures in vitro and increase double-strand breaks and deletions in vivo. Enhancer mutability depends on DNA replication direction and is caused by TG-dinucleotide repeats. Modeling shows that elevated mutation rates can influence evolution under demographic conditions relevant for sticklebacks and humans. DNA fragility may thus help explain why the same loci are often used repeatedly during parallel adaptive evolution.

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Journal ArticleDOI

The population genetics of structural variants in grapevine domestication

TL;DR: It is found that strong purifying selection acts against SVs but particularly against inversion and translocation events, and SVs nonetheless accrue as recessive heterozygotes in clonally propagated lineages, suggesting roles in domestication.
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Convergent regulatory evolution and loss of flight in paleognathous birds

TL;DR: This work combined phylogenomic, developmental, and epigenomic analysis of 11 new genomes of paleognathous birds to show that convergent evolution of regulatory regions, more so than protein-coding genes, is prevalent among developmental pathways associated with independent losses of flight.
Journal ArticleDOI

At the Beginning of the End and in the Middle of the Beginning: Structure and Maintenance of Telomeric DNA Repeats and Interstitial Telomeric Sequences.

TL;DR: This review compares the mechanisms of maintenance and dynamic properties of telomeric repeats and ITSs and discusses the implications of these dynamics on genome stability.
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Non-B DNA: a major contributor to small- and large-scale variation in nucleotide substitution frequencies across the genome.

TL;DR: In this article, the authors conducted a comprehensive analysis of nucleotide substitution frequencies at non-B DNA loci within non-coding, non-repetitive genome regions, their ±2 kb flanking regions, and 1-Megabase windows, using human-orangutan divergence and human single-nucleotide polymorphisms.
Journal ArticleDOI

The Role of Mutation Bias in Adaptive Evolution.

TL;DR: Little support is found for mutation bias as an independent force in adaptive evolution, although it can interact with selection under conditions of small population size and when standing genetic variation is limited, entirely consistent with standard evolutionary theory.
References
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Journal ArticleDOI

Fast and accurate short read alignment with Burrows–Wheeler transform

TL;DR: Burrows-Wheeler Alignment tool (BWA) is implemented, a new read alignment package that is based on backward search with Burrows–Wheeler Transform (BWT), to efficiently align short sequencing reads against a large reference sequence such as the human genome, allowing mismatches and gaps.
Journal ArticleDOI

A global reference for human genetic variation.

Adam Auton, +517 more
- 01 Oct 2015 - 
TL;DR: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and has reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-generation sequencing, deep exome sequencing, and dense microarray genotyping.
Journal ArticleDOI

An integrated map of structural variation in 2,504 human genomes

Peter H. Sudmant, +87 more
- 01 Oct 2015 - 
TL;DR: In this paper, the authors describe an integrated set of eight structural variant classes comprising both balanced and unbalanced variants, which are constructed using short-read DNA sequencing data and statistically phased onto haplotype blocks in 26 human populations.
Journal ArticleDOI

Adaptation from standing genetic variation

TL;DR: There is potential to distinguish between adaptation from standing variation and that from new mutations by differences in the genomic signature of selection.
Journal ArticleDOI

Widespread Parallel Evolution in Sticklebacks by Repeated Fixation of Ectodysplasin Alleles

TL;DR: The authors used positional cloning methods to identify the major chromosome locus controlling armor plate patterning in wild threespine sticklebacks and found that members of this clade of low-plated alleles are present at low frequencies in marine fish, which suggests that standing genetic variation can provide a molecular basis for rapid, parallel evolution of dramatic phenotypic change in nature.
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