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Genome editing excisase origins illuminated by somatic genome of Blepharisma

Minakshi SinghiD, Brandon Kwee Boon SeahiD, Christiane EmmerichiD, Aditi D. SinghiD, Christian WoehleiD, Bruno HüetteliD, Adam ByerlyiD, Naomi A. StoveriD, Mayumi Sugiura, Terue Harumoto, Estienne Carl SwartiD

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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.

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Brandon Kwee Boon Seah, Minakshi Singh, Christiane Emmerich+8 more·bioRxiv·May 2, 2022· 1 citations