@article{67d834d8e50b4ac2b1b3d7dfbbb2aa72,
title = "Multiple and independent phases of transposable element amplification in the genomes of piciformes (woodpeckers and allies)",
abstract = "The small and conserved genomes of birds are likely a result of flight-relatedmetabolic constraints. Recombination-driven deletions andminimal transposable element (TE) expansions have led to continually shrinking genomes during evolution of many lineages of volant birds. Despite constraints of genome size in birds, we identified multiple waves of amplification of TEs in Piciformes (woodpeckers, honeyguides, toucans, and barbets). Relative to other bird species' genomic TE abundance (<10% of genome), we found ∼17-30% TE content inmultiple cladeswithin Piciformes. Several families of the retrotransposon superfamily chicken repeat 1 (CR1) expanded in at least three different waves of activity. The most recent CR1 expansions (∼4-7% of genome) preceded bursts of diversification in the woodpecker clade and in the American barbets + toucans clade. Additionally, we identified several thousand polymorphic CR1 insertions (hundreds per individual) in three closely related woodpecker species. Woodpecker CR1 insertion polymorphisms are maintained at lower frequencies than single nucleotide polymorphisms indicating that purifying selection is acting against additional CR1 copies and that these elements impose a fitness cost on their host. These findings provide evidence of large scale and ongoing TE activity in avian genomes despite continual constraint on genome size.",
keywords = "CR1, Diversification, Genomics, Transposable elements, Woodpeckers",
author = "Manthey, {Joseph D.} and Moyle, {Robert G.} and St{\'e}phane Boissinot",
note = "Funding Information: We thank Mark Robbins at the University of Kansas Biodiversity Institute for assistance with all tissue loans. Much of the data analyses were performed using the high-performance computing cluster at New York University in Abu Dhabi. We thank Marc Arnoux from the Genome Core Facility at NYUAD for assistance with genome sequencing. This work was supported by New York University Abu Dhabi (NYUAD) research funds AD180 (to S.B.) and National Science Foundation DEB-1241181 and DEB-1557053 (to R.G.M.). The NYUAD Sequencing Core is supported by NYUAD Research Institute grant G1205-1205A to the NYUAD Center for Genomics and Systems Biology. Funding Information: We thank Mark Robbins at the University of Kansas Biodiversity Institute for assistance with all tissue loans. Much of the data analyses were performed using the highperformance computing cluster at New York University in Abu Dhabi. We thank Marc Arnoux from the Genome Core Facility at NYUAD for assistance with genome sequencing. This work was supported by New York University Abu Dhabi (NYUAD) research funds AD180 (to S.B.) and National Science Foundation DEB-1241181 and DEB- 1557053 (to R.G.M.). The NYUAD Sequencing Core is supported by NYUAD Research Institute grant G1205-1205A to the NYUAD Center for Genomics and Systems Biology. Publisher Copyright: {\textcopyright} The Author(s) 2018.",
year = "2018",
month = jun,
day = "1",
doi = "10.1093/gbe/evy105",
language = "English (US)",
volume = "10",
pages = "1445--1456",
journal = "Genome biology and evolution",
issn = "1759-6653",
publisher = "Oxford University Press",
number = "6",
}