CERATOSEX

Identification and Characterisation of the Sex Locus in the Dioecious Moss Ceratodon purpureus

 Coordinatore UNIVERSITY OF LEEDS 

 Organization address address: WOODHOUSE LANE
city: LEEDS
postcode: LS2 9JT

contact info
Titolo: Mr.
Nome: Martin
Cognome: Hamilton
Email: send email
Telefono: +44 113 343 4090
Fax: +44 113 343 0949

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 309˙235 €
 EC contributo 309˙235 €
 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-2012-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-09-01   -   2015-08-31

 Partecipanti

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

 Organization address address: WOODHOUSE LANE
city: LEEDS
postcode: LS2 9JT

contact info
Titolo: Mr.
Nome: Martin
Cognome: Hamilton
Email: send email
Telefono: +44 113 343 4090
Fax: +44 113 343 0949

UK (LEEDS) coordinator 309˙235.20

Mappa


 Word cloud

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

determining    deep       linked    gene    chromosomes    transcriptomic    sequencing    genome    determination    regions    genes    purpureus    evolution       sex    haploid   

 Obiettivo del progetto (Objective)

In genetically controlled sexual systems, gender is determined by defined chromosomal regions or by complete sex chromosomes. Both types have emerged independently and repeatedly during evolution. The structure, function and evolution of a number of sex determining regions (SDRs) have been studied in diploid organisms, but little is known about sex determination in haploid systems. The dioecious bryophyte Ceratodon purpureus presents an interesting subject for the study of evolution of sex not only because it is haploid but also because of its phylogenetic position as a basal plant. Deep transcriptomic analysis using next-generation sequencing will be performed in order to identify sex specific regions of the genome. Sex-related genes will be identified by deep transcriptomic sequencing of a segregating population. Genes controlling sex-determination should be localised within non-recombining regions of the sex chromosomes. X- and Y-linked genes identified as candidate sex-determining loci will be functionally tested using the high-frequency gene targeting technology possible in both C. purpureus and its hermaphrodite relative Physcomitrella patens. Because deep transcriptome analysis generates gene sequences on a genome-wide scale, it will be possible to compare rates of evolution between X- and Y-linked genes, and between autosomally located genes.

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