ESYMBIOSIS

Molecular Basis of Coral Symbiosis

 Coordinatore RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG 

 Organization address address: SEMINARSTRASSE 2
city: HEIDELBERG
postcode: 69117

contact info
Nome: Brigitta
Cognome: Martin
Email: send email
Telefono: +49 6221 545677
Fax: +49 6221 545678

 Nazionalità Coordinatore Germany [DE]
 Totale costo 100˙000 €
 EC contributo 100˙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-2013-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-05-01   -   2018-04-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG

 Organization address address: SEMINARSTRASSE 2
city: HEIDELBERG
postcode: 69117

contact info
Nome: Brigitta
Cognome: Martin
Email: send email
Telefono: +49 6221 545677
Fax: +49 6221 545678

DE (HEIDELBERG) coordinator 100˙000.00

Mappa


 Word cloud

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establishment    cnidaria    bleaching    larval    coral    techniques    phylum    environmental    molecular    cellular    corals    aiptasia    symbiosis    first    dinoflagellates   

 Obiettivo del progetto (Objective)

'Coral reefs are the world's most diverse marine ecosystems and their existence depends upon a functional intracellular symbiosis between dinoflagellates (single-celled algae) and their coral host. Stresses, such as elevated seawater temperature, cause the obligate symbiosis to break down, a phenomenon known as coral “bleaching”. Incidences of coral bleaching worldwide are on the rise, linked to global climate change. Most corals (phylum Cnidaria) first initiate symbiosis with dinoflagellates (genus Symbiodinium) during larval stages. The molecular basis of coral symbiosis is not well understood, mainly because corals are difficult to work with and have slow generation times. I propose to use an emerging model system based on the small, experimentally tractable sea anemone Aiptasia (phylum Cnidaria) to analyze symbiosis establishment at the cellular and molecular level, including the ways in which symbiosis establishment is affected by environmental changes. First, I will establish a thorough cellular description of symbiosis establishment in Aiptasia larvae. Next, I will identify conserved genes involved in larval symbiosis in cnidarians and use molecular techniques to dissect their functions. Finally, I will establish gain-of function techniques (transgenesis) for Aiptasia using microinjection into early embryos to visualize membranes, nuclei and the cytoskeleton during symbiosis establishment using life imaging. Analysis of coral symbiosis at the cellular and molecular level will provide the missing link between existing genomic approaches and field population-level approaches and will help identify measures to protect coral symbiosis in the face of environmental change.'

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