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  Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes

Han, Z., Sieriebriennikov, B., Susoy, V., Lo, W.-S., Igreja, C., Dong, C., et al. (2022). Horizontally Acquired Cellulases Assist the Expansion of Dietary Range in Pristionchus Nematodes. Molecular Biology and Evolution, 39(2): msab370. doi:10.1093/molbev/msab370.

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 Creators:
Han, Z1, Author           
Sieriebriennikov, B1, Author           
Susoy, V1, Author           
Lo, W-S1, Author           
Igreja, C1, 2, Author           
Dong, C1, Author           
Berasategui, A, Author                 
Witte, H1, Author           
Sommer, RJ1, Author           
Affiliations:
1Department Integrative Evolutionary Biology, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3371685              
2Regulation and Post-Translational Modification of Gene Expression in Nematodes Group, Department Integrative Evolutionary Biology, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3507708              

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 Abstract: Horizontal gene transfer (HGT) enables the acquisition of novel traits via non-Mendelian inheritance of genetic material. HGT plays a prominent role in the evolution of prokaryotes, whereas in animals, HGT is rare and its functional significance is often uncertain. Here, we investigate horizontally acquired cellulase genes in the free-living nematode model organism Pristionchus pacificus. We show that these cellulase genes 1) are likely of eukaryotic origin, 2) are expressed, 3) have protein products that are secreted and functional, and 4) result in endo-cellulase activity. Using CRISPR/Cas9, we generated an octuple cellulase mutant, which lacks all eight cellulase genes and cellulase activity altogether. Nonetheless, this cellulase-null mutant is viable and therefore allows a detailed analysis of a gene family that was horizontally acquired. We show that the octuple cellulase mutant has associated fitness costs with reduced fecundity and slower developmental speed. Furthermore, by using various Escherichia coli K-12 strains as a model for cellulosic biofilms, we demonstrate that cellulases facilitate the procurement of nutrients from bacterial biofilms. Together, our analysis of cellulases in Pristionchus provides comprehensive evidence from biochemistry, genetics, and phylogeny, which supports the integration of horizontally acquired genes into the complex life history strategy of this soil nematode.

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 Dates: 2022-02
 Publication Status: Issued
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 Rev. Type: -
 Identifiers: DOI: 10.1093/molbev/msab370
PMID: 34978575
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Title: Molecular Biology and Evolution
  Other : Mol. Biol. Evol.
Source Genre: Journal
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Publ. Info: Oxford : Oxford University Press
Pages: 16 Volume / Issue: 39 (2) Sequence Number: msab370 Start / End Page: - Identifier: ISSN: 0737-4038
CoNE: https://pure.mpg.de/cone/journals/resource/954925536119