NCRNAP

Structural and functional studies of the interaction between non coding RNAs and the RNA polymerase

 Coordinatore DEMOCRITUS UNIVERSITY OF THRACE 

 Organization address address: PANEPISTIMIOUPOLI
city: KOMOTINI
postcode: 69100

contact info
Titolo: Prof.
Nome: Nicholas M
Cognome: Glykos
Email: send email
Telefono: +30 25510 30620
Fax: +30 25510 30620

 Nazionalità Coordinatore Greece [EL]
 Totale costo 45˙000 €
 EC contributo 45˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2010-RG
 Funding Scheme MC-ERG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-03-01   -   2014-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    DEMOCRITUS UNIVERSITY OF THRACE

 Organization address address: PANEPISTIMIOUPOLI
city: KOMOTINI
postcode: 69100

contact info
Titolo: Prof.
Nome: Nicholas M
Cognome: Glykos
Email: send email
Telefono: +30 25510 30620
Fax: +30 25510 30620

EL (KOMOTINI) coordinator 45˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

   rnap    polymerase    life    transcription    expression    play    rna       specificity    forms    upon    stationary    small    ray    crystallography    shown    gene    regulation    dna    rnas    sigma   

 Obiettivo del progetto (Objective)

'It was a surprise of the last decade the large number of small, noncoding RNAs, which have been identified to play regulatory roles in the modulation of gene expression in all kingdoms of life. The bacterial 6S RNA is a transcription regulator of the σ70-RNA polymerase holoenzyme during the stationary phase. It has been shown that 6S binds with high affinity and specificity onto the σ70-RNAP and presumably blocks the sites of interaction of RNAP with DNA promoters. It has also been shown that upon outgrowth from the stationary phase 6S serves as template for the RNAP and the product RNAs, which are synthesized, destabilize the complex and liberate the polymerase from 6S RNA. The objective of this proposal is the structure determination of the whole complex between 6S and σ70-RNAP, of truncated forms and sub-assemblies by X-ray crystallography. The project will involve the preparation of RNA-protein complexes in amounts, purity and homogeneity suitable for studies with X-ray crystallography. The obtained structural information will help to understand the nature of 6S regulation of transcription in details. It will also help to elucidate the features which determine the σ70-RNAP specificity for 6S RNA interactions and may allow us to understand the molecular mechanism of RNAP liberation upon product RNAs synthesis.'

Introduzione (Teaser)

Small non-coding RNAs play a key role in regulation of gene expression in all life forms. Recent research has highlighted their role in regulation of the DNA material chromatin.

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