Publications by authors named "Monika Zakrzewska-Placzek"

U1 snRNP (U1 small nuclear ribonucleoprotein) is a nuclear ribonucleoprotein complex involved mainly in pre-mRNA splicing, which is a key regulatory process in the eukaryotic gene expression pathway, but also in the process of preventing premature transcription termination (telescripting). U1 snRNP interacts directly with RNA polymerase II, thereby influencing the synthesis and maturation of transcripts in the cell nucleus, including the formation of the 3' end of mRNA and polyadenylation. At the level of cell physiology, it regulates the functioning of mitochondria and energy metabolism.

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Cytoplasmic mRNA decay is effected by exonucleolytic degradation in either the 5' to 3' or 3' to 5' direction. Pervasive terminal uridylation is implicated in mRNA degradation, however, its functional relevance for bulk mRNA turnover remains poorly understood. In this study, we employ genome-wide 3'-RACE (gw3'-RACE) in the model system fission yeast to elucidate the role of uridylation in mRNA turnover.

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Background: NOL12 5'-3' exoribonucleases, conserved among eukaryotes, play important roles in pre-rRNA processing, ribosome assembly and export. The most well-described yeast counterpart, Rrp17, is required for maturation of 5.8 and 25S rRNAs, whereas human hNOL12 is crucial for the separation of the large (LSU) and small (SSU) ribosome subunit rRNA precursors.

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The DXO family of proteins participates in eukaryotic mRNA 5'-end quality control, removal of non-canonical NAD+ cap and maturation of fungal rRNA precursors. In this work, we characterize the Arabidopsis thaliana DXO homolog, DXO1. We demonstrate that the plant-specific modification within the active site negatively affects 5'-end capping surveillance properties of DXO1, but has only a minor impact on its strong deNADding activity.

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Article Synopsis
  • Arabidopsis thaliana has two nuclear exonucleases, XRN2 and XRN3, which are similar to yeast and human proteins involved in RNA processing and transcription termination.
  • When XRN3 is knocked down, it leads to changes in the expression of many genes and results in the buildup of transcripts that have not been properly capped or polyadenylated due to incomplete termination of RNA polymerase II.
  • The study indicates that the disruption caused by the lack of XRN3 can affect gene expression significantly by allowing read-through transcription, which may produce harmful RNA-mRNA chimeras and trigger the formation of small interfering RNAs (siRNAs).
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Article Synopsis
  • Proper regulation of ribosome biosynthesis is crucial for cell growth and requires precise control, as abnormal ribosome production can lead to severe developmental issues and genetic diseases.
  • Eukaryotic ribosome biogenesis involves processing precursor ribosomal RNA (pre-rRNA) into mature rRNAs, which must be coordinated with RNA modification, folding, and assembly with ribosomal proteins.
  • The text explores various ribonucleases that play a role in pre-rRNA processing, examining their biochemical properties, regulatory mechanisms, and how these factors interact across different eukaryotic organisms like yeast, plants, and humans.
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The role of the nucleus of a eukaryotic cell during gene expression is not only limited to transcription and RNA processing but also includes the initial stages of RNA surveillance. All of these processes, and more precisely, transcription elongation and termination, 5'-end RNA maturation, and the removal of processing intermediates and aberrant molecules, require the activity of the nuclear 5'-3' exoribonuclease Rat1/Xrn2. This protein, together with its cytoplasmic counterpart, Xrn1, constitutes a highly conserved eukaryotic family of nucleases, whose roles exceed participation in RNA metabolism alone.

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Three Rat1/Xrn2 homologues exist in Arabidopsis thaliana: nuclear AtXRN2 and AtXRN3, and cytoplasmic AtXRN4. The latter has a role in degrading 3' products of miRNA-mediated mRNA cleavage, whereas all three proteins act as endogenous post-transcriptional gene silencing suppressors. Here we show that, similar to yeast nuclear Rat1, AtXRN2 has a role in ribosomal RNA processing.

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