FP6Индивидуална стипендия2005–2008

STARTSITE · Structural studies of the RNA polymerase II transcription machinery: mechanism of start site selection

6РП — Действия „Мария Кюри“

Период
2005-04-01 → 2008-03-31
Финансиране от ЕС
253 429 €
Участници
2
Схема
OIF

Линиите свързват координатора с партньорите. За проекти отпреди 2014 г. CORDIS не винаги дава точни координати. Тези точки са на ниво град или държава.

Накратко на български

РНК полимераза II и нейните помощни фактори определят точното място в ДНК, от което започва синтезът на РНК. Разбирането на този механизъм помага за създаването на общ молекулярен модел за стартирането на транскрипцията при различните еукариоти.

Този кратък обзор е генериран от изкуствен интелект

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

Цел на проекта

The current application concerns the mechanisms of transcription initiation in eukaryotic cells. The postdoc-project will be carried out in Prof. Roger D. Kornberg's laboratory at Stanford University, California.THE SPECIFIC AIM of the project is a molecular understanding of how RNA polymerase II (RNAP II) together with the general transcription factors (GTFs) can recognize promoter DNA and initiate RNA synthesis at a specific genomic location.Reports have shown that RNAP II and TFIIB are solely responsible for this process, but the underlying mechanism is still not known. Recently the structure of a RNAP II/TFIIB cocrystal has been solved in budding yeast. The transcription start site differs however in this yeast compared to fission yeast and most other eukaryotes including human so a general model for the selection process could not be elucidated from this structure.OUR MAIN OBJECTIVES are to do structural analysis of a RNAP II/TFIIB complex in fission yeast with X-ray crystallography and compare it to t he budding yeast structure. We will complement the structural information with mutational analysis of TFIIB in a pure in vitro transcription system derived from fission yeast developed by me as a Ph.D. student.THE OVERALL GOAL with the project is to generate a general molecular model for the transcription start site selection process.My stay will lead to the acquirement of new technological knowledge such as structural analysis of multi-protein complexes with X-ray crystallography that I believe will be a vibrant scientific field in the future.I will also be able to develop a scientific network that will be useful for my future career as a scientist, as well as the European community, after my return to Sweden.

Оригинален текст от CORDIS (на английски).

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Данни: CORDIS, © Европейски съюз