scholarly journals Cryo-EM and antisense targeting of the 28-kDa frameshift stimulation element from the SARS-CoV-2 RNA genome

Author(s):  
Kaiming Zhang ◽  
Ivan N. Zheludev ◽  
Rachel J. Hagey ◽  
Raphael Haslecker ◽  
Yixuan J. Hou ◽  
...  
Keyword(s):  
2004 ◽  
Vol 10 (30) ◽  
pp. 3741-3756 ◽  
Author(s):  
Jordi Gomez ◽  
Anna Nadal ◽  
Rosario Sabariegos ◽  
Nerea Beguiristain ◽  
Maria Martell ◽  
...  

Life ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 344
Author(s):  
Kevin Nicolas Calderon ◽  
Johan Fabian Galindo ◽  
Clara Isabel Bermudez-Santana

Zika virus (ZIKV), without a vaccine or an effective treatment approved to date, has globally spread in the last century. The infection caused by ZIKV in humans has changed progressively from mild to subclinical in recent years, causing epidemics with greater infectivity, tropism towards new tissues and other related symptoms as a product of various emergent ZIKV–host cell interactions. However, it is still unknown why or how the RNA genome structure impacts those interactions in differential evolutionary origin strains. Moreover, the genomic comparison of ZIKV strains from the sequence-based phylogenetic analysis is well known, but differences from RNA structure comparisons have barely been studied. Thus, in order to understand the RNA genome variability of lineages of various geographic distributions better, 410 complete genomes in a phylogenomic scanning were used to study the conservation of structured RNAs. Our results show the contemporary landscape of conserved structured regions with unique conserved structured regions in clades or in lineages within circulating ZIKV strains. We propose these structures as candidates for further experimental validation to establish their potential role in vital functions of the viral cycle of ZIKV and their possible associations with the singularities of different outbreaks that lead to ZIKV populations to acquire nucleotide substitutions, which is evidence of the local structure genome differentiation.


2006 ◽  
Vol 80 (24) ◽  
pp. 12197-12208 ◽  
Author(s):  
Klaus K. Orlinger ◽  
Verena M. Hoenninger ◽  
Regina M. Kofler ◽  
Christian W. Mandl

ABSTRACT Flaviviruses have a monopartite positive-stranded RNA genome, which serves as the sole mRNA for protein translation. Cap-dependent translation produces a polyprotein precursor that is co- and posttranslationally processed by proteases to yield the final protein products. In this study, using tick-borne encephalitis virus (TBEV), we constructed an artificial bicistronic flavivirus genome (TBEV-bc) in which the capsid protein and the nonstructural proteins were still encoded in the cap cistron but the coding region for the surface proteins prM and E was moved to a separate translation unit under the control of an internal ribosome entry site element inserted into the 3′ noncoding region. Mutant TBEV-bc was shown to produce particles that packaged the bicistronic RNA genome and were infectious for BHK-21 cells and mice. Compared to wild-type controls, however, TBEV-bc was less efficient in both RNA replication and infectious particle formation. We took advantage of the separate expression of the E protein in this system to investigate the role in viral assembly of the second transmembrane region of protein E (E-TM2), a second copy of which was retained in the cap cistron to fulfill its other role as an internal signal sequence in the polyprotein. Deletion analysis and replacement of the entire TBEV E-TM2 region with its counterpart from another flavivirus revealed that this element, apart from its role as a signal sequence, is important for virion formation.


Hepatology ◽  
2018 ◽  
Vol 67 (6) ◽  
pp. 2096-2112 ◽  
Author(s):  
Wenshi Wang ◽  
Yijin Wang ◽  
Changbo Qu ◽  
Shan Wang ◽  
Jianhua Zhou ◽  
...  

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