YRNAcleave · Sequence and structural requirements for Y RNA cleavage
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2016-08-01 → 2018-07-31
- Финансиране от ЕС
- 195 455 €
- Участници
- 1
- Схема
- MSCA-IF-EF-ST
Линиите свързват координатора с партньорите.
Накратко на български
Y-РНК молекулите в човешките клетки се разграждат на по-къси фрагменти, като например при Y5 РНК. Разбирането на този процес помага да се разбере как се регулира експресията на гените.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Sequence and structural requirements for Y RNA cleavage
"Small non-coding RNAs play important roles in gene expression regulation. Initially the attention was focused on the 21-24-nucleotide small RNAs such as microRNAs but later on deeper sequencing experiments using next generation sequencing revealed a slightly longer class of small RNAs that are 30-34 nucleotides long. These longer small RNAs are often generated from known non-coding RNAs such as tRNA or snoRNA. The biogenesis of these longer small RNAs seems to be diverse and is not well understood. The host laboratory have characterised the biogenesis of such longer small RNAs generated from Y RNAs in mammalian cells and found that it is different from microRNA biogenesis but also from the way tRNA derived small RNAs are produced. Y RNAs are ~100 nt long molecules, first discovered owing to their association with the autoimmune proteins Ro60 and La. The four Y RNAs (Y1, Y3, Y4 and Y5) show high evolutionary conversation in the animal kingdom, with humans possessing the full complement of Y RNA genes and some species, such as mouse, only retaining the Y1 and Y3 RNA genes. Y RNAs bind a range of proteins within the cell, notably the toroid shaped protein Ro60 involved in RNA quality control, and the La protein which has a range of implicated functions (Figure 1). Not all Y RNAs however are found within ribonucleoprotein complexes. The non-protein bound Y RNAs have been shown to be essential for the initiation of chromosomal DNA replication by acting as licensing factors in post-midblastula transition (MBT) stage cells. The overall objective of the project is to understand the process of Y RNA fragmentation in human cells. The project consisted of four specific objectives: Objective 1 Validation of sequencing results for pools 1-3, Objective 2 Mutagenesis of 5' arm of Y5 RNA, Objective 3 Validation of mutations in the Y5 5' sRNA region and Objective 4 Testing ""designer"" mutants. We describe the results and conclusions in the next section. "
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Small non-coding RNAs play important roles in gene expression regulation. Initially the attention was focused on the 21-24-nucleotide small RNAs such as microRNAs but later on deeper sequencing experiments using next generation sequencing revealed a slightly longer class of small RNAs that are 30-34 nucleotides long. These longer small RNAs are often generated from known non-coding RNAs such as tRNA or snoRNA. The biogenesis of these longer small RNAs seems to be diverse and is not well understood. The host laboratory have characterised the biogenesis of such longer small RNAs generated from Y RNAs in mammalian cells and found that it is different from microRNA biogenesis but also from the way tRNA derived small RNAs are produced. Results from a high-throughput mutagenesis approach suggest that the secondary structure of the Y RNA, rather than its sequence, determines where the cleavage happens that liberates the small RNAs from the 3' end of Y RNAs. This project aims validating these results and also to apply a high-throughput mutagensis screen on the 5' region of the Y RNA to study the production of small RNAs from that end of the molecule. Combining the results for Y RNA derived longer small RNA generation from both 5' and 3' end of these molecules will enable the experienced researcher to establish how this class of small RNAs are produced by designing specific novel mutants and test them in mammalian cells. Another aim of the project is to give training to the experienced researcher in mammalian cell biology and bioinformatics to add his existing molecular biology and microbiology skills.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITY OF EAST ANGLIA · NorwichКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз
