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SPP 1384:  Mechanisms of Genome Haploidisation

Subject Area Biology
Term from 2009 to 2015
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 72844389
 
During cell division each chromosome must be faithfully duplicated into two sister chromatids, which must then be properly segregated to generate daughter cells with a genome of high integrity and of the same ploidy as that of the parent cell. There is one exception critical for reproductive life and for human health: genome haploidisation to produce functional germ cells. In meiosis, the genome is initially duplicated but then reduced in two subsequent divisions steps to haploidy. Despite the obvious importance of the process of genome haploidisation, without which no germ cells could be generated in man, in most other vertebrates, and in most lower eukaryotes, we understand very little about its mechanics, its regulation, and the key factors that drive genome haploidisation.
Errors in meiotic genome haploidisation are a major cause for aneuploidies such as down syndrome or for infertility, which affects about ten percent of couples. Thus, genome haploidisation is of enormous significance for human health. Specific areas of research within this Priority Programme include meiotic chromosome architecture, chromosome dynamics, DNA recombination and -repair, transcription, cell cycle control, spindle assembly and cytokinesis. These topics are addressed using a wide range of experimental model systems - from yeast to mouse - and cellular and molecular approaches.
DFG Programme Priority Programmes
International Connection Switzerland

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