BMC

Bacteria with Multiple Chromosomes: Interplay between genome architecture and cell physilogy

 Coordinatore INSTITUT PASTEUR 

 Organization address address: RUE DU DOCTEUR ROUX 25-28
city: PARIS CEDEX 15
postcode: 75724

contact info
Titolo: Dr.
Nome: Marie-Laure
Cognome: Rosso
Email: send email
Telefono: +33 44 38 95 26
Fax: +33 40 61 39 40

 Nazionalità Coordinatore France [FR]
 Totale costo 201˙932 €
 EC contributo 201˙932 €
 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-2011-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-03-01   -   2015-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUT PASTEUR

 Organization address address: RUE DU DOCTEUR ROUX 25-28
city: PARIS CEDEX 15
postcode: 75724

contact info
Titolo: Dr.
Nome: Marie-Laure
Cognome: Rosso
Email: send email
Telefono: +33 44 38 95 26
Fax: +33 40 61 39 40

FR (PARIS CEDEX 15) coordinator 201˙932.40

Mappa


 Word cloud

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

genomic    strains    gene    genome    orici    oricii    techniques    chromosomes    replication    cholera    relative   

 Obiettivo del progetto (Objective)

'Bacteria with Multiple-Chromosomes (BMC) are relatively frequent. This project was designed to understand the advantages of such a genomic organization. Based on observations from comparative genomics these could be: shorter generation time by providing additional origins of replication, a differential chromosome copy number regulation that changes relatives gene doses of the unlinked gene sets and physical separation of the “core genome” and the “flexible genome” genes. This project will focus principally on the two last hypotheses addressing them experimentally using leading-edge techniques. Vibrio cholera will be used as model. Its genome consists of two circular chromosomes that vary in their origin of replication (oriCI and oriCII respectively). The project will study extensively rearranged V. cholera strains obtained through genomic engineering techniques. Monochromosomal under oriCI or oriCII derivatives will be employed. Strains where both chromosomes will be under oriCI or oriCII control will also be analyzed. All strains transcriptomes will be analyzed using Illumina RNA-seq. These studies will show to what extent variation in genome structure can affect the relative gene expression. The exploration of the relative accessibility of the two chromosomes to DNA integration will be probed. These experiments will contribute to understand differences in architecture plasticity, gene content and lack of genetic flux between both chromosomes. The proposed researcher profile matches to project needs. The host institution has all facilities needed. All former trainees of the proposed supervisor have progressed in their academic careers. Hence the project is feasible and has great chances to be completed successfully. EU excellence and competiveness in Science will benefit from training shuch an excellent applicant in the best scientific environment and will give the chance to generate a long-term collaboration with Argentina.'

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