FP6Индивидуална стипендия2007–2009

RRNA SURVEILLANCE · A focus on degradation of ribosomal RNAs by the TRAMP/exosome RNA surveillance machinery

6РП — Действия „Мария Кюри“

Период
2007-10-01 → 2009-09-30
Финансиране от ЕС
162 448 €
Участници
1
Схема
EIF

Линиите свързват координатора с партньорите.

Накратко на български

Процесът на създаване на рибозоми и начинът, по който клетката контролира качеството на рибозомната РНК, са в центъра на анализа. Разбирането на тези механизми помага да се изясни връзката между сглобяването на рибозомите и развитието на рак.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Final Activity Report Summary - RRNA SURVEILLANCE (A focus on degradation of ribosomal RNAs by the TRAMP/exosome RNA surveillance machinery)

Ribosomes, the large RNA-protein complexes that translate mRNA into protein in the cytoplasm of eukaryotic cells, are largely synthesized in a subnuclear compartment called the nucleolus. Synthesis of ribosomal RNA (rRNA) and ribosome assembly are tightly coordinately regulated and require the activity of more than 150 protein factors, underscoring the complexity of this process. Deregulation of steps in ribosome biogenesis is often associated with alterations in cell cycle, cell proliferation and cell growth and often contributes to increased susceptibility to cancer. Indeed, aberrant nucleolar morphology is often a hallmark for cancer cells. However, the molecular mechanism underlying the link between cancer and the activity of nucleolar proteins is largely unknown. A detailed understanding of ribosome biogenesis and how it is regulated will help us comprehend the links found between ribosome assembly and cancer. The objectives of this study were to understand how and where in the cell the production of rRNA is monitored. The biggest achievement made during the funding period was to develop a technology that allows researchers to figure out where proteins interact with the RNA during the assembly of ribosomes. The project used this technology to generate a map of protein-RNA interactions in pre-ribosomes. The results of these studies are widely considered a breakthrough in the ribosome assembly field and will have long term impact on the field for years to come.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Nuclear surveillance and degradation of aberrant RNA requires the TRAMP complex, which promotes exosome-mediated degradation in the nucleus by adding poly (A) tails to aberrant RNAs. Interestingly, a mutant yeast strain defective in nuclear export of 60S preribosomes (sda1-2) accumulates ribosomal proteins, the TRAMP complex and the nuclear exosome in a punctate nucleolar structure, suggesting that preribosomes are degraded here.To address if in this structure is a general site for TRAMP-exosome mediated degradation of polyadenylated non-coding RNAs, I will use several fluorescence microscopy detection techniques to determine if other known degradation enzymes and non-coding RNAs targeted for degradation accumulate in this focus. Pre-mRNA surveillance by the nuclear exosome involves interactions with chromatin, transcription elongation factors, pre-mRNA processing factors and export factors and likely occurs co-transcriptionally. To determine if a similar surveillance mechanism exists for pre-rRNA processing.

Оригинален текст от CORDIS (на английски).

Участници

Връзки

Данни: CORDIS, © Европейски съюз