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  Beggars can’t be choosers: developmental integration of a horizontally-acquired gene by co-option

Sieriebriennikov, B., Susoy, V., Roedelsperger, C., Riebesell, M., Akduman, N., Boichenko, I., et al. (2017). Beggars can’t be choosers: developmental integration of a horizontally-acquired gene by co-option. Poster presented at 2nd Biennial Meeting of the Pan-American Society for Evolutionary Developmental Biology (PASEDB 2017), Calgary, Canada.

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Sieriebriennikov, B1, Author                 
Susoy, V1, Author                 
Roedelsperger, C1, Author                 
Riebesell, M1, Author                 
Akduman, N1, Author           
Boichenko, I1, Author                 
Sommer, RJ1, Author                 
Affiliations:
1Department Integrative Evolutionary Biology, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3375786              

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 Abstract: Horizontal gene transfer is the passage of genetic material between phylogenetically distant lineages. Using whole-genome sequencing platforms, horizontally-acquired genes have been identified in numerous organisms including eukaryotes. However, to become functional, new genes must be integrated into gene regulatory networks, and little is known about how this is achieved. We studied developmental integration of a horizontally-acquired cellulase cel-2 in the nematode Pristionchus pacificus. We show that cel-2 is expressed in pharyngeal gland cells and the secretory-excretory system, consistent with the presumptive extracorporeal hydrolytic function of the encoded enzyme. Strikingly, cel-2 expression is tightly linked to the regulation of a dimorphism of feeding structures. We observe that cel-2 is more highly expressed in the ‘stenostomatous’ microbivorous morph than in the ‘eurystomatous’ morph that can kill other nematodes. Using mutants in the developmental switch genes eud-1 and nhr-40, which regulate the mouth-form decision, we could elucidate that these genes also regulate the level and pattern of cel-2 expression. In addition, cel-2 expression is influenced by bacteria provided to the worm as food and is increased upon starvation. We conclude that a horizontally-acquired cellulase gene in P. pacificus was integrated into development by co-option of existing regulators of feeding plasticity.

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 Dates: 2019-07
 Publication Status: Published online
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Title: 2nd Biennial Meeting of the Pan-American Society for Evolutionary Developmental Biology (PASEDB 2017)
Place of Event: Calgary, Canada
Start-/End Date: 2017-08-19 - 2017-08-23
Invited: Yes

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Title: 2nd Biennial Meeting of the Pan-American Society for Evolutionary Developmental Biology (PASEDB 2017)
Source Genre: Proceedings
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Pages: - Volume / Issue: - Sequence Number: 111 Start / End Page: 103 - 104 Identifier: -