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Abstract
Most of our knowledge of insect genomes comes from Holometabolous species, which undergo complete metamorphosis and have genomes typically under 2 Gb with little signs of DNA methylation. In contrast, Hemimetabolous insects undergo the presumed ancestral process of incomplete metamorphosis, and have larger genomes with high levels of DNA methylation. Hemimetabolous species from the Orthopteran order (grasshoppers and crickets) have some of the largest known insect genomes. What drives the evolution of these unusual insect genome sizes, remains unknown. Here we report the sequencing, assembly and annotation of the 1.66-Gb genome of the Mediterranean field cricket Gryllus bimaculatus, and the annotation of the 1.60-Gb genome of the Hawaiian cricket Laupala kohalensis. We compare these two cricket genomes with those of 14 additional insects and find evidence that hemimetabolous genomes expanded due to transposable element activity. Based on the ratio of observed to expected CpG sites, we find higher conservation and stronger purifying selection of methylated genes than non-methylated genes. Finally, our analysis suggests an expansion of the pickpocket class V gene family in crickets, which we speculate might play a role in the evolution of cricket courtship, including their characteristic chirping.
Ylla, Extavour et al. use genomic data from crickets to investigate the evolution of large genome sizes and DNA methylation events in insects. Their findings indicate that transposable element activity drove genome expansion in hemimetabolous insects, such as crickets and grasshoppers, and that DNA methylation is predominant in conserved genes.
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1 Harvard University, Department of Organismic and Evolutionary Biology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)
2 Harvard University, Department of Organismic and Evolutionary Biology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); National Institute for Basic Biology, Okazaki, Japan (GRID:grid.419396.0) (ISNI:0000 0004 0618 8593)
3 Tokyo Institute of Technology, School of Life Science and Technology, Tokyo, Japan (GRID:grid.32197.3e) (ISNI:0000 0001 2179 2105)
4 National Institute of Genetics, Comparative Genomics Laboratory, Shizuoka, Japan (GRID:grid.288127.6) (ISNI:0000 0004 0466 9350); National Institute of Genetics, Advanced Genomics Center, Shizuoka, Japan (GRID:grid.288127.6) (ISNI:0000 0004 0466 9350)
5 Tokushima University, Department of Bioscience and Bioindustry, Tokushima, Japan (GRID:grid.267335.6) (ISNI:0000 0001 1092 3579)
6 Okayama University, Graduate School of Medicine, Pharmacology and Dentistry, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472)
7 Tokushima University, Graduate School of Advanced Technology and Science, Tokushima, Japan (GRID:grid.267335.6) (ISNI:0000 0001 1092 3579)
8 Tokushima University, Department of Bioscience and Bioindustry, Tokushima, Japan (GRID:grid.267335.6) (ISNI:0000 0001 1092 3579); National University of, Department of Biological Sciences, Singapore, Singapore (GRID:grid.4280.e) (ISNI:0000 0001 2180 6431)
9 Harvard University, Department of Organismic and Evolutionary Biology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); DeSales University, Department of Natural Sciences, Center Valley, USA (GRID:grid.446642.6)
10 Harvard University, Department of Organismic and Evolutionary Biology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Harvard University, Department of Molecular and Cellular Biology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)