Abstract
Meiosis reduces the ploidy of the genome to generate haploid gametes for sexual reproduction. As gametes are portals for the generational transfer of genetic material, it is imperative that the genome is copied accurately and that chromosomes segregate equally into each haploid gamete. Proper chromosome segregation requires the formation of specialized chromosome axes to create and maintain an environment competent for double-strand break (DSB) formation and homologous recombination. Although the fundamental copying mechanism appears to be identical in mitosis and meiosis, the S phase that precedes meiosis (meiS) is at least twice as long as mitotic S phase (mitS) [1]–[4]. The underlying basis for an extended S phase prior to meiosis has, until now, been mysterious. While it is postulated that meiS length contributes to the dramatic chromosome reorganization that occurs during meiotic prophase (Figure 1), there is conflicting data concerning the interdependencies of meiS, chromosome morphogenesis, and DSB formation [5]–[9]. In this issue of PLoS Genetics, Blitzblau et al. [10] use innovative genome-wide approaches in yeast to elucidate mechanisms underlying meiS length and provide insight into the relationship between DNA replication and meiotic prophase events. Figure 1 Meiotic DNA replication, chromosome axes, and DSB formation.
Highlights
Meiosis reduces the ploidy of the genome to generate haploid gametes for sexual reproduction
The authors found that Mcm bound to a significant fraction of the same origins in both mitosis and meiosis; the few that differed were located near cycle-specific, actively transcribed genes, consistent with studies suggesting competition between replication and transcription machinery [11]
The number of early firing origins increased, but not to the level utilized in mitotic cells, suggesting nucleotide depletion contributes to delayed origin firing and meiS timing
Summary
Meiosis reduces the ploidy of the genome to generate haploid gametes for sexual reproduction. Delayed Origin Firing Slows Meiotic S Phase The authors found that Mcm bound to a significant fraction of the same origins in both mitosis and meiosis; the few that differed were located near cycle-specific, actively transcribed genes, consistent with studies suggesting competition between replication and transcription machinery [11].
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