Publications by authors named "O Yu Burenina"

Article Synopsis
  • - The study focuses on 6S RNA, a small non-coding RNA that mimics DNA promoters, effectively binding to bacterial RNA polymerase (RNAP) to inhibit gene transcription, particularly during stationary growth or starvation phases.
  • - The synthesis of short product RNA (pRNA) from the 6S RNA template is influenced by specific interactions between the 6S RNA and RNAP, as well as secondary channel factors, which modulate the transcription process.
  • - Researchers utilized a molecular beacon assay to track the release of 6S RNA during pRNA synthesis, revealing that mutations in specific RNAP regions affect the kinetics of 6S RNA release and suggesting a regulatory role of universal transcription factors in both pRNA synthesis and
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A lot of long non-coding RNAs (lncRNAs) are expressed in human cells in a number of transcripts of different lengths and composition of exons. In case of cancer-associated lncRNAs, an actual task is to determine their specific isoforms, since each transcript can perform its own function in carcinogenesis and might have a unique expression profile in various types of tumors. For the first time, we analyzed the expression of CASC8 lncRNA in human pancreatic ductal adenocarcinoma cell lines and found an abundant isoform that was previously considered as the minor one in this type of cancer.

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6S RNA, a small non-coding RNA present in almost all bacteria, inhibits transcription via direct binding to RNA polymerase holoenzymes. The mechanism of 6S RNA action was investigated to a large extent in , however, lack of 6S RNA (Δ) was demonstrated to be unfavorable but not essential for cell survival under various growth conditions. In the present study, we revealed, for the first time, a lethal phenotype of the Δ strain in the presence of high concentrations of HO.

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Successful detection of very small RNAs (tiny RNAs, ~8-15 nt in length) by northern blotting depends on tailored protocols with respect to transfer and immobilization on membranes as well as design of sensitive detection probes. For RNA crosslinking to positively charged membranes, we compared UV light with chemical RNA crosslinking by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC), using either denaturing or native polyacrylamide gels. We show that northern blot detection of tiny RNAs with 5'-digoxigenin-labeled DNA/LNA mixmer probes is a highly sensitive and specific method and, in our hands, more sensitive than using a corresponding DNA/LNA mixmer probe with a 5'-P-end-label.

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