Differential Conservation and Loss of Chicken Repeat 1 (CR1) Retrotransposons in Squamates Reveal Lineage-Specific Genome Dynamics Across Reptiles

Author:

Gable Simone M1ORCID,Bushroe Nicholas A1,Mendez Jasmine M1,Wilson Adam1,Pinto Brendan J23ORCID,Gamble Tony345ORCID,Tollis Marc1ORCID

Affiliation:

1. School of Informatics, Computing, and Cyber Systems, Northern Arizona University , Flagstaff, AZ , USA

2. Center for Evolution and Medicine, Arizona State University , Tempe, AZ , USA

3. Department of Zoology, Milwaukee Public Museum , Milwaukee, WI , USA

4. Department of Biological Sciences, Marquette University , Milwaukee, WI , USA

5. Bell Museum of Natural History, University of Minnesota , St. Paul, MN , USA

Abstract

Abstract Transposable elements (TEs) are repetitive DNA sequences which create mutations and generate genetic diversity across the tree of life. In amniote vertebrates, TEs have been mainly studied in mammals and birds, whose genomes generally display low TE diversity. Squamates (Order Squamata; including ∼11,000 extant species of lizards and snakes) show as much variation in TE abundance and activity as they do in species and phenotypes. Despite this high TE activity, squamate genomes are remarkably uniform in size. We hypothesize that novel, lineage-specific genome dynamics have evolved over the course of squamate evolution. To understand the interplay between TEs and host genomes, we analyzed the evolutionary history of the chicken repeat 1 (CR1) retrotransposon, a TE family found in most tetrapod genomes which is the dominant TE in most reptiles. We compared 113 squamate genomes to the genomes of turtles, crocodilians, and birds and used ancestral state reconstruction to identify shifts in the rate of CR1 copy number evolution across reptiles. We analyzed the repeat landscapes of CR1 in squamate genomes and determined that shifts in the rate of CR1 copy number evolution are associated with lineage-specific variation in CR1 activity. We then used phylogenetic reconstruction of CR1 subfamilies across amniotes to reveal both recent and ancient CR1 subclades across the squamate tree of life. The patterns of CR1 evolution in squamates contrast other amniotes, suggesting key differences in how TEs interact with different host genomes and at different points across evolutionary history.

Funder

National Science Foundation

State of Arizona Technology Research Initiative Fund

National Institutes of Health

Publisher

Oxford University Press (OUP)

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