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  Genome editing excisase origins illuminated by somatic genome of the ciliate Blepharisma

Singh, M., Seah, B., Emmerich, C., Singh, A., Woehle, C., Huettel, B., et al. (2022). Genome editing excisase origins illuminated by somatic genome of the ciliate Blepharisma. In The 41st Annual Meeting of the DGP (pp. 26).

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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
Sover, NA, Author
Sugiura, M, Author
Harumoto, C, 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 present 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: 2022-07
 Publication Status: Published online
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Title: The 41st Annual Meeting of the German Society for Protozoology (DGP 2022)
Place of Event: Bergisch Gladbach, Germany
Start-/End Date: 2022-07-12 - 2022-07-15

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Title: The 41st Annual Meeting of the DGP
Source Genre: Proceedings
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Pages: - Volume / Issue: - Sequence Number: - Start / End Page: 26 Identifier: -