Publications by authors named "Tsimafei Navalayeu"

Article Synopsis
  • Williams-Beuren syndrome (WBS) is caused by a deletion of genes on chromosome 7, leading to a variety of health issues due to protein malfunction.
  • The role of the protein methyltransferase WBSCR27 in WBS remains unclear, prompting researchers to create gene knockout mouse cell lines to identify its methylation targets.
  • Through structural analysis, they discovered that WBSCR27 has a characteristic Class I methyltransferase structure, and binding to S-adenosyl-L-homocysteine (SAH) helps form a substrate binding site, suggesting areas for future investigation.
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Genes coding for small peptides have been frequently misannotated as long noncoding RNA (lncRNA) genes. Here we have demonstrated that one such transcript is translated into a 56-amino-acid-long peptide conserved in chordates, corroborating the work published while this manuscript was under review. The Mtln peptide could be detected in mitochondria of mouse cell lines and tissues.

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Peptides encoded by short open reading frames (sORFs) are usually defined as peptides ≤100 aa long. Usually sORFs were ignored by automatic genome annotation programs due to the high probability of false discovery. However, improved computational tools along with a high-throughput RIBO-seq approach identified a myriad of translated sORFs.

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N6-methyladenosine (m(6)A) is ubiquitously present in the RNA of living organisms from Escherichia coli to humans. Methyltransferases that catalyze adenosine methylation are drastically different in specificity from modification of single residues in bacterial ribosomal or transfer RNA to modification of thousands of residues spread among eukaryotic mRNA. Interactions that are formed by m(6)A residues range from RNA-RNA tertiary contacts to RNA-protein recognition.

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