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Projekt Druckansicht

Die Evolution der Xylophagie in Bockkäfern: Vielfalt, Entwicklungsgeschichte und funktionelle Charakterisierung pflanzliche Zellwand abbauender Enzyme in Käfern der Familie Cerambycidae

Antragsteller Dr. Yannick Pauchet
Fachliche Zuordnung Biochemie und Physiologie der Tiere
Evolution, Anthropologie
Ökologie und Biodiversität der Tiere und Ökosysteme, Organismische Interaktionen
Förderung Förderung von 2017 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 386747961
 
Erstellungsjahr 2022

Zusammenfassung der Projektergebnisse

We managed to extract high-molecular-weight DNA of high quality and to generate draft genome assemblies for four species, including Rhamnusium bicolor (Lepturinae), Aromia moschata and Molorchus minor (Cerambycinae), and Exocentrus adspersus (Lamiinae). - We generated a species phylogeny based on 305 single-copy orthologous genes extracted from these genomes and other beetle ones that were publicly available. We confirmed the monophyly of the family Cerambycidae, its close relationship to the Chrysomelidae and its integration into the Phytophaga clade. - We confirmed that newly discovered families of PCWDEs in species of Cerambycidae were indeed encoded by beetle’s genomes. Genes encoding these enzymes all contain introns and are surrounded by genes commonly found in the genome of other insect species. - We also show a perfect correlation between the PCWDE families present in our cerambycid transcriptomes and in the corresponding draft genomes, but we annotated more genes per family in the latter compared to the former. Surprisingly, we observed low level of microsynteny in genome regions containing genes encoding PCWDEs compared to what we were expecting, apart between species belonging to the same subfamily. Altogether, these “low quality” draft genomes provided extra insights on our understanding of the evolution of HGT-acquired PCWDEs in Phytophaga beetles. However, we had just enough high-molecular-weight DNA for MinION sequencing – this type of sequencing being prone to sequencing errors – and were not able to polish these draft genome assemblies with Illumina short reads. This is probably the main drawback of our approach.

Projektbezogene Publikationen (Auswahl)

 
 

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