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Recombination,Pairing, and Synapsis of Homologs during Meiosis
Authors:Denise Zickler  Nancy Kleckner
Institution:1.Institut de Génétique et Microbiologie, UMR 8621, Université Paris-Sud, 91405 Orsay, France;2.Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138
Abstract:Recombination is a prominent feature of meiosis in which it plays an important role in increasing genetic diversity during inheritance. Additionally, in most organisms, recombination also plays mechanical roles in chromosomal processes, most notably to mediate pairing of homologous chromosomes during prophase and, ultimately, to ensure regular segregation of homologous chromosomes when they separate at the first meiotic division. Recombinational interactions are also subject to important spatial patterning at both early and late stages. Recombination-mediated processes occur in physical and functional linkage with meiotic axial chromosome structure, with interplay in both directions, before, during, and after formation and dissolution of the synaptonemal complex (SC), a highly conserved meiosis-specific structure that links homolog axes along their lengths. These diverse processes also are integrated with recombination-independent interactions between homologous chromosomes, nonhomology-based chromosome couplings/clusterings, and diverse types of chromosome movement. This review provides an overview of these diverse processes and their interrelationships.The role of the meiotic program is to generate gametes having half the chromosome complement of the original progenitor cell. This task is accomplished by occurrence of a single round of DNA replication followed by two successive rounds of chromosome segregation. Homologs segregate to opposite poles at meiosis I, then sisters separate to opposite poles in meiosis II, analogously to mitosis (Fig. 1A).Open in a separate windowFigure 1.General features of meiosis. (A) At meiosis I, homologs segregate; at meiosis II, sisters segregate. At metaphase I (left), maternal (red) and paternal (black) chromosomes are held together by a chiasma comprising a reciprocal crossover (CO) plus connections along sister arms, which are released during segregation. (B) Monochiasmate bivalent of Locusta after bromodeoxyuridine (BrdU) incorporation. Differential staining of the sister chromatids confirms that exchange has occurred, for example, between red and purple chromatids in corresponding drawings. (From Jones 1987; reprinted, with permission, from Academic Press © 1987.) (C) Diplotene bivalent of grasshopper with three chiasmata (arrows) and corresponding drawing. (From Jones and Franklin 2006; reprinted, with permission, from Elsevier © 2006.) (D) Top: Meiotic prophase in rye microsporocytes; chromosomes are stained by hematoxylin (pictures by D.Z.). Bottom: corresponding timing of the recombination steps from double-strand breaks (DSBs) to COs; timing of intermediates as in budding yeast (Hunter 2007). SEI, Single-end invasion; dHJ, double Holliday junction; SDSA, synthesis-dependent strand annealing; NCO, noncrossover.During meiosis, a central role of recombination is to increase genetic diversity. However, recombination is also essential for two fundamental features unique to meiotic chromosome mechanics: pairing and segregation of homologous chromosomes (“homologs”). Pairing is mediated by the totality of programmed interhomolog recombinational interactions in association with chromosome structural axes (see below). Segregation is mediated specifically by the carefully chosen subset of those interactions that mature into crossover (CO) products. During segregation of homologs, just as for segregation of sister chromatids, the separating entities must be connected to one another such that regular bipolar alignment on the spindle results in tension on centromere/kinetochore complexes. When all segregating pairs are properly aligned and under tension, anaphase is triggered. Segregation of sisters is ensured by connections between sister centromere/kinetochore regions. Segregation of homologs is ensured by connections along chromosome arms that are provided by the combined effects of an interhomolog CO plus links between sisters (Fig. 1A). These connections can be seen cytologically as chiasmata (Fig. 1B,C). In organisms in which meiosis occurs without recombination, other features have evolved that hold homologs together to ensure regular segregation (Zickler and Kleckner 1998, 1999; reviewed in Stewart and Dawson 2008; Tsai and McKee 2011; Lake and Hawley 2012; Obeso et al. 2014).
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