Menu
MapConnectionsTopicsBulgariaThe Night (K-TRIO)Marie Skłodowska-CurieFor studentsFor teachersMethodologySurprise me
H2020Individual fellowship2019–2021

RNAfate · revealing regulation of cellular “noise”.

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2019-09-01 → 2021-08-31
EU contribution
€173,076
Participants
1
Scheme
MSCA-IF-EF-ST

Lines connect the coordinator with its partners.

Results in brief

RNAfate- revealing regulation of cellular “noise”.

RNA is an essential element in the flow of genetic information in the cell. Recent development of genome-wide technologies revealed multiple novel RNA transcripts, mostly non-coding (nc) for proteins. Their biological role in the cell is still poorly understood and at first they were considered as “noise”. During the recent decade, research has revealed growing evidence for the importance of ncRNAs in organism development and disease. Thus, further clarification of their functions remains a pressing need in the field. Among the ncRNA group, a subset of RNAs of at least 200 nucleotides, called long non-coding (lnc)RNAs, are of mayor interest. LncRNAs share many features with messenger RNA, but they cannot be translated into proteins. In some cases, even small changes in amount of some of the lncRNA in the cell can have a big impact on a cell or an entire organism. Thus, regulation of their levels is crucial to prevent undesired effects. After ncRNA synthesis the next key processes modulating amount of RNA in the cell is degradation. This ultimate step of RNA regulation is the focus of this work. Most of key proteins responsible for lncRNA removal in nucleus in human cells are already characterized. However cytoplasmic fate of lncRNAs remain less understood. Therefore, taking advantage of the advancement of high throughput RNA sequencing technology and novel genetic tools for the modification of genes in human cells, this project focused on defining the key exonucleolytic enzymes responsible for regulation of lncRNA levels in the cytoplasm of human cells, as well as identifying hidden or previously not detected lncRNAs.

Data: CORDIS, © European Union

Project objective

RNA is an essential element in the flow of genetic information in the cell. Recent development of genome-wide techniques reveal multiple novel RNA transcripts, mostly non-coding (nc) for protein. Their significance for the cell is still poorly understood and at first they were considered as “noise”. During the recent decade research has revealed growing evidence for the importance of ncRNAs in cell development and disease. Further elaboration of their functions remains a pressing need in the field. To address this gap in knowledge we will focus on clarifying their regulation. One of key processes modulating levels of RNA in the cell is degradation. Xrn1 is a highly conserved 5’-3’ exoribonuclease that plays an important role in RNA decay. At the Institut Curie the Morillon’s group has discovered that a class of long non-coding (lnc)RNAs is highly sensitive to Xrn1-decay in yeast. The XRN1 sequence is well-conserved from yeast to human, but very little is known about human (h)Xrn1 targets other than mRNAs. Recent studies have revealed involvement of human lncRNAs in cancerogenesis or viral infection. Moreover, studies of Hepatitis C virus (HCV) have shown that viral infection change ncRNA levels. Others have reported that viral structured (sf)RNA can inhibit hXrn1. But how this sfRNA affect ncRNA-om was not yet determined. Importantly, Xrn1 can localize to cytoplasmic foci called P-bodies which are dynamic reservoirs of multiple RNAs and proteins involved in processes such RNA silencing or RNA decay. It has been demonstrated that P-bodies are altered in multiple human diseases and upon viral infection. There are three objectives for this project: 1) identifying novel members of the hXrn1-sensitive coding and noncoding transcriptome, 2) understanding, on a genome-wide scale, how the impairment of hXrn1 by viral sfRNA can change ncRNA stability, as well as their potential role in infection 3) defining the effect of hXrn1 impairment on P-body formation and composition.

Original text from CORDIS.

Participants

  • INSTITUT CURIE · ParisCoordinatorFrance

Links

Data: CORDIS, © European Union