4.5 Article

Survey Sequencing Reveals Elevated DNA Transposon Activity, Novel Elements, and Variation in Repetitive Landscapes among Vesper Bats

Journal

GENOME BIOLOGY AND EVOLUTION
Volume 4, Issue 4, Pages 575-585

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evs038

Keywords

transposon; survey sequencing; Chiroptera

Funding

  1. National Science Foundation (NSF) [MCB-0841821, DEB-1020865, MCB-1052500, DEB-1020890]
  2. Mississippi Agricultural and Forestry Experiment Station
  3. Louisiana Board of Regents [LEQSF-2006-09]
  4. Academy of Sciences of the Czech Republic [AVO-Z50510513]

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The repetitive landscapes of mammalian genomes typically display high Class I (retrotransposon) transposable element (TE) content, which usually comprises around half of the genome. In contrast, the Class II (DNA transposon) contribution is typically small (<3% in model mammals). Most mammalian genomes exhibit a precipitous decline in Class II activity beginning roughly 40 Ma. The first signs of more recently active mammalian Class II TEs were obtained from the little brown bat, Myotis lucifugus, and are reflected by higher genome content (similar to 5%). To aid in determining taxonomic limits and potential impacts of this elevated Class II activity, we performed 454 survey sequencing of a second Myotis species as well as four additional taxa within the family Vespertilionidae and an outgroup species from Phyllostomidae. Graph-based clustering methods were used to reconstruct the major repeat families present in each species and novel elements were identified in several taxa. Retrotransposons remained the dominant group with regard to overall genome mass. Elevated Class II TE composition (3-4%) was observed in all five vesper bats, while less than 0.5% of the phyllostomid reads were identified as Class II derived. Differences in satellite DNA and Class I TE content are also described among vespertilionid taxa. These analyses present the first cohesive description of TE evolution across closely related mammalian species, revealing genome-scale differences in TE content within a single family.

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