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The stem-loop II motif (s2m) is an RNA element present in viruses from divergent viral families, including astroviruses and coronaviruses, but its functional significance is unknown. We created deletions or substitutions of the s2m in astrovirus VA1 (VA1), classic human astrovirus 1 (HAstV1) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). For VA1, recombinant virus could not be rescued upon partial deletion of the s2m or substitutions of G-C base pairs. Compensatory substitutions that restored the G-C base-pair enabled recovery of VA1. For HAstV1, a partial deletion of the s2m resulted in decreased viral titers compared to wild-type virus, and reduced activity in a replicon system. In contrast, deletion or mutation of the SARS-CoV-2 s2m had no effect on the ability to rescue the virus, growth , or growth in Syrian hamsters. Our study demonstrates the importance of the s2m is virus-dependent.
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http://dx.doi.org/10.1101/2022.04.30.486882 | DOI Listing |
Noncoding RNA
July 2025
Unidad de Biología Integrativa, Centro de Investigación Científica de Yucatán, Calle 43, No. 130, Chuburná de Hidalgo, Mérida CP 97205, Yucatán, Mexico.
: snoRNAs have traditionally been known for their role as guides in post-transcriptional rRNA modifications. Previously, our research group identified several RNAs that may bind to PIP2 with LIPRNA-seq. Among them, snR191 stood out due to its potential specific interaction with this lipid, distinguishing itself from other snoRNAs.
View Article and Find Full Text PDFNat Commun
August 2025
Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo Kashiwa, Chiba, Japan.
The N-methyladenosine (mA) modification in U6 snRNA, catalyzed by METTL16 using S-adenosylmethionine (SAM) as the methyl donor, is required for efficient and accurate pre-mRNA splicing. However, the mechanism by which METTL16 modifies U6 snRNA with mA remains elusive. Here, we present cryo-EM structures of METTL16 in complex with U6 snRNA, providing insights into the METTL16-mediated modification of U6 snRNA with mA.
View Article and Find Full Text PDFBiomol NMR Assign
July 2025
Institute for Organic Chemistry and Chemical Biology, Johann Wolfgang Goethe University, Max-von-Laue-Straße7, 60438, Frankfurt/M, Germany.
Due to the emergence of the SARS-CoV-2 virus, research on coronaviruses has been massively accelerated. In addition to SARS-CoV-2, there are other human coronaviruses, including HCoV-229E. In all coronaviruses, secondary structure predictions indicate the presence of conserved structural elements in the 5'-untranslated region (5'-UTR).
View Article and Find Full Text PDFACS Phys Chem Au
July 2025
Department of Chemistry and Biochemistry, Duquesne University, Pittsburgh, Pennsylvania 15282, United States.
The three-dimensional (3D) atomistic-resolution structure and dynamics of RNA kissing complexes (KCs) and extended duplexes (EDs), homodimers formed through palindromic base pairing, are crucial for understanding viral replication and structure-informed therapeutic design. Polyacrylamide gel electrophoresis (PAGE) evidence suggests KC and ED dimer formation between stem-loop II motif (s2m) elements in SARS-CoV, SARS-CoV-2, and Delta SARS-CoV-2, which may regulate host immune response. However, the absence of 3D structural data on s2m dimers limits structural interpretation needed to explain differences in stability indicated by native PAGE and biophysical implications.
View Article and Find Full Text PDFNucleic Acids Res
July 2025
Department of Chemistry & Biochemistry, Florida State University, Tallahassee, FL 32306, United States.
La-related proteins (LARPs) are RNA-binding proteins that are involved in a variety of disease-related processes. Most LARPs recognize short single-stranded poly(U/A) motifs via a conserved hydrophobic pocket. Human LARP6 (HsLARP6) is an exception, binding a structured 5' stem-loop (5'SL) that controls type I collagen translation and fibroproliferative disease progression.
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