EVOSPERM

Sexual selection and the evolutionary biology of spermatogenesis

 Coordinatore UNIVERSITAET BASEL 

 Organization address address: Petersplatz 1
city: BASEL
postcode: 4003

contact info
Titolo: Dr.
Nome: Lukas
Cognome: Schärer
Email: send email
Telefono: +41 61 267 03 66
Fax: +41 61 267 03 62

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 180˙970 €
 EC contributo 180˙970 €
 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-2009-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-04-01   -   2012-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET BASEL

 Organization address address: Petersplatz 1
city: BASEL
postcode: 4003

contact info
Titolo: Dr.
Nome: Lukas
Cognome: Schärer
Email: send email
Telefono: +41 61 267 03 66
Fax: +41 61 267 03 62

CH (BASEL) coordinator 180˙970.80

Mappa


 Word cloud

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

sexual    reproduction    little    plasticity    variation    macrostomum    evolutionary    genetic    species    machinery    morphology    male    phenotypic    traits    sperm    spermatogenesis    evolution   

 Obiettivo del progetto (Objective)

'Spermatogenesis is of fundamental importance to reproduction and fertility, yet several of its features remain enigmatic. Why, for example, do sperm display such extraordinary morphological diversity, when their basic function differs little from one species to another? And why are sperm produced in such large quantities, vastly exceeding the number of eggs produced by females? Sexual selection, the evolutionary force proposed by Charles Darwin 150 years ago, provides the most promising framework to answer these questions. We now recognize sexual selection can modify traits such as sperm morphology and sperm numbers whenever these enhance male fertilization success in competition with other males. However, there remain significant barriers to our understanding of how these traits evolve, because we know very little about either their genetic architecture or about how selection on sperm morphology or sperm numbers impacts on the machinery of spermatogenesis. To transform our understanding in these areas, we will use the highly amenable Macrostomum flatworms as a model to understand sperm evolution. First, we will conduct a quantitative genetic analysis in M. lignano of sperm morphology and numbers, plus a broad suite of additional male and female traits that are likely to affect sperm evolution. We will assess (a) genetic variation in and correlations between these traits and (b) the genetics of phenotypic plasticity in each trait. Second, we will apply immunocytochemical techniques to explore variation in the kinetics of spermatogenesis over both ecological and evolutionary timescales. We will test for (a) phenotypic plasticity; (b) genetic variation between inbred lines; and (c) divergence between related Macrostomum species with radically different sperm production requirements. Establishing how sexual selection shapes the complex machinery and products of spermatogenesis will provide widely applicable insights into the evolutionary biology of reproduction.'

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