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Projekt Druckansicht

Analyse und Änderung von 2'-O-Methylierungsmustern der ribosomalen RNAs in Sulfolobus acidocaldarius

Fachliche Zuordnung Stoffwechselphysiologie, Biochemie und Genetik der Mikroorganismen
Allgemeine Genetik und funktionelle Genomforschung
Förderung Förderung von 2016 bis 2020
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 315648833
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

2′-O-methylation is the most abundant modification of ribosomal RNAs in hyperthermophilic Archaea. Archaea utilize ribonucleoprotein (RNP) complexes containing small (s)RNAs to identify targets for 2′-O-methylation. These RNAs are termed C/D box sno-like RNAs (C/D box sRNA) in archaea and resemble their eukaryotic snoRNA counterparts in structure and function. They are characterized by conserved sequence elements called box C and C′ and box D and D′. These elements fold into a ubiquitous RNA structural motif, the kink-turn (k-turn). Two k-turn elements flank short, highly variable guide sequences that exhibit complementarity to sequences within rRNA. Consequently, each C/D box sRNA contains a combination of two guide sequences that specify target methylation sites via base complementarity, directing the activity of the methyltransferase fibrillarin. Two copies of the L7Ae protein bind and stabilize the k-turn motifs. In this project, we aimed to investigate the targeting potential of the C/D box sRNAs that were identified in S. acidocaldarius. Additionally, we aimed to establish a methodology that allows for the global analysis of methylation sites. After submission of this proposal, several groups reported methods to achieve this goal and we were able to utilize available methodology in collaboration with Prof. Gordon Carmichael (University of Connecticut). However, these analyses also highlighted problems for the differentiation of modification sites and artefacts caused by highly stable rRNA structures. Analysis of the individual C/D box sRNA guide sequences of S. acidocaldarius allowed for two surprising observations. First, we discovered that C and D boxes are often formed due to overlap with start and stop codons of proteincoding genes allowing for accelerated evolution of the C/D box guide pairs. Second, individual k-turns, representing half C/D box sRNA molecules, were found to be fused to mRNAs, impacting their stability and allowing for their gene regulation. Regulated genes include l7ae and other C/D box sRNA binding partners, enabling negative feedback. These finding highlighted that the accelerated evolution of C/D box sRNA genes allow for a 2′-O-methylation landscape of rRNAs with high plasticity and the potential to evolve novel paired methylation sites that can stabilize rRNA interactions during folding.

Projektbezogene Publikationen (Auswahl)

 
 

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