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Genome editing excisase origins illuminated by somatic genome of Blepharisma

MPS-Authors
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Singh,  M
Research Group Ciliate Genomics and Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society;

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Seah,  BKB
Research Group Ciliate Genomics and Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society;

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Emmerich,  C
Research Group Ciliate Genomics and Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society;

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Singh,  A
Research Group Ciliate Genomics and Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society;

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Swart,  EC
Research Group Ciliate Genomics and Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society;

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Citation

Singh, M., Seah, B., Emmerich, C., Singh, A., Woehle, C., Huettel, B., et al. (submitted). Genome editing excisase origins illuminated by somatic genome of Blepharisma.


Abstract
Massive DNA excision occurs regularly in ciliates, ubiquitous microbial eukaryotes with somatic and germline nuclei in the same cell. Tens of thousands of internally eliminated sequences (IESs) scattered throughout a copy of the ciliate germline genome are deleted during development of the streamlined somatic genome. Blepharisma represents one of the two earliest diverging ciliate classes, and, unusually, has dual pathways of somatic nuclear development, making it ideal for investigating the functioning and evolution of these processes. Here, we report the somatic genome assembly of Blepharisma stoltei strain ATCC 30299 (41 Mb), arranged as numerous alternative telomere-capped minichromosomes. This genome encodes eight PiggyBac transposase homologs liberated from transposons. All are subject to purifying selection, but just one, the putative IES excisase, has a complete catalytic triad. We propose PiggyBac homologs were ancestral excisases that enabled evolution of extensive, natural genome editing.