Chromosome dynamics of the early meiotic cell cycle in S. cerevisiae

In every cell cycle the genetic material must be duplicated and transmitted to the daughter cells. Meiosis is a developmental program that allows a diploid cell to produce haploid progeny. The reduction in chromosome number obtained during meiosis requires specialized mechanisms that are absent during the canonical mitotic cell cycle. Although previous studies found strong similarities between pre-mitotic and pre-meiotic DNA replication, pre-meiotic S phase is longer than pre-mitotic S phase, suggesting that meiosis-specific events regulate the rate of DNA replication. Additionally, after DNA replication, homologous recombination is initiated by the introduction of hundreds DNA double-strand breaks (DSBs) into the genome to produce physical DNA exchanges, or crossovers, between homologous chromosomes. To investigate the chromosome dynamics of the early meiotic cell cycle, I performed comprehensive analysis of pre-meiotic DNA replication and DSB formation in budding yeast. Genome-wide studies of pre-meiotic DNA replication confirmed that the same replication origins are selected and activated in pre-meiotic and pre-mitotic cells, although replication was delayed at a large number of origins. These results indicate that the regulation of DNA replication is similar in the meiotic and mitotic cell cycles, but that the replication-timing program differs. Elimination of meiosis-specific cohesion or homologous recombination had no effect on the number or identity of early pre-meiotic origins. Analysis of cells sporulated in the presence of the replication inhibitor HU revealed a Cln3-dependent inhibition of meiotic entry. To map the locations of meiotic DSBs, I developed a method to detect meiotic ssDNA. Examination of the sites of ssDNA enrichment indicated that DSBs occur mainly in the promoters of active genes, consistent with previous studies of individual DSB sites.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Biology.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2008

Author dc:creator

• Blitzblau, Hannah G

Advisor dc:contributor.advisor

• Stephen P. Bell.

• Biology.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/42402

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/42402