MEIOSIS2012

Chromosome segregation during meiosis

Coordinatore	UNIVERZITA KOMENSKEHO V BRATISLAVE    more  Organization address address: SAFARIKOVO NAM 6 city: Bratislava 1 postcode: 81499 contact info Titolo: Mrs. Nome: Beata Cognome: Rajnáková Email: send email Telefono: 421260000000 Fax: 421260000000
Nazionalità Coordinatore	Slovakia [SK]
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-2012-CIG
Funding Scheme	MC-CIG
Anno di inizio	2013
Periodo (anno-mese-giorno)	2013-03-01   -   2017-02-28

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	UNIVERZITA KOMENSKEHO V BRATISLAVE  Organization address address: SAFARIKOVO NAM 6 city: Bratislava 1 postcode: 81499 contact info Titolo: Mrs. Nome: Beata Cognome: Rajnáková Email: send email Telefono: 421260000000 Fax: 421260000000	SK (Bratislava 1)	coordinator	100˙000.00

Mappa

 Word cloud

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

 Obiettivo del progetto (Objective)

'Sexual reproduction depends on the generation of haploid gametes from diploid progenitor cells in a process called meiosis. Although we understand certain aspects of meiosis, some of the key regulators of meiotic chromosome segregation are still missing and only now we do have tools to systematically identify these proteins and to determine their function. In this project, we want to screen the recently released S. pombe knock-out collection to identify mutants missegregating chromosomes during meisosis. Our priority will be to characterize mutants defective in mono-orientation of sister kinetochores during the first meiotic division, as this is the least understood aspect of meiotic chromosome segregation. The fission yeast S. pombe is an excellent model organism for such studies due to the fact that S. pombe kinetochores, like those of most eukaryotic cells, are associated with multiple microtubules. Moreover, it is amenable to both genetic and cell biology techniques and highly synchronous meiosis can be induced. In order to understand the function of identified proteins, we will combine genetic, biochemial and cell biology techniques. We believe that it is important to understand mechanisms governing meiotic chromosome segregation. Meiosis is not only a fundamental and fascinating process, it is also vital to fertility and human health. Defects in chromosome segregation during meiosis are the major cause of miscarriages, birth defects, infertility and genetic disorders such as Down Syndrome. The potential benefits of thorough understanding of chromosome segregation during meiosis are impressive. They could reveal much about the mechanism of gamete development and sexual reproduction with implications for diagnostics and treatment of infertility, certain cancers and genetic diseases.'