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  Genome editing excisase origins illuminated by somatic genome of Blepharisma

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.

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 Creators:
Singh, M1, Author           
Seah, BKB1, Author           
Emmerich, C1, Author           
Singh, A1, Author           
Woehle, C, Author
Huettel, B, Author
Byerly, A, Author
Stover, NA, Author
Sugiura, M, Author
Harumoto, T, Author
Swart, EC1, Author           
Affiliations:
1Research Group Ciliate Genomics and Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3375053              

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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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 Dates: 2022-04
 Publication Status: Submitted
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1101/2021.12.14.471607
 Degree: -

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