RNA secondary structure at the transcription start site influences EBOV transcription initiation and replication in a length- and stability-dependent manner

• Published in: RNA biology Vol. 18; no. 4; pp. 523 - 536
• Main Authors: Bach, Simone, Demper, Jana-Christin, Biedenkopf, Nadine, Becker, Stephan, Hartmann, Roland K.
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 03.04.2021
• Subjects: EBOV 3ʹ-leader promoter; expansion of the spacer between PE1 and PE2; Research Paper; RNA stabilization of hairpin structures at the transcription start site (TSS); Viral transcription and replication; Viral transcription and replication; expansion of the spacer between PE1 and PE2; RNA stabilization of hairpin structures at the transcription start site (TSS); EBOV 3ʹ-leader promoter
• ISSN: 1547-6286; 1555-8584
• DOI: 10.1080/15476286.2020.1818459

Ebola virus (EBOV) RNA has the potential to form hairpin structures at the transcription start sequence (TSS) and reinitiation sites of internal genes, both on the genomic and antigenomic/mRNA level. Hairpin formation involving the TSS and the spacer sequence between promotor elements (PE) 1 and 2 was suggested to regulate viral transcription. Here, we provide evidence that such RNA structures form during RNA synthesis by the viral polymerase and affect its activity. This was analysed using monocistronic minigenomes carrying hairpin structure variants in the TSS-spacer region that differ in length and stability. Transcription and replication were measured via reporter activity and by qRT-PCR quantification of the distinct viral RNA species. We demonstrate that viral RNA synthesis is remarkably tolerant to spacer extensions of up to ~54 nt, but declines beyond this length limit (~25% residual activity for a 66-nt extension). Minor incremental stabilizations of hairpin structures in the TSS-spacer region and on the mRNA/antigenomic level were found to rapidly abolish viral polymerase activity, which may be exploited for antisense strategies to inhibit viral RNA synthesis. Finally, balanced viral transcription and replication can still occur when any RNA structure formation potential at the TSS is eliminated, provided that hexamer phasing in the promoter region is maintained. Altogether, the findings deepen and refine our insight into structure and length constraints within the EBOV transcription and replication promoter and suggest a remarkable flexibility of the viral polymerase in recognition of PE1 and PE2.