Tessé Sophie, Bourbon Henri-Marc, Debuchy Robert, Budin Karine, Dubois Emeline, Liangran Zhang, Antoine Romain, Piolot Tristan, Kleckner Nancy, Zickler Denise, Espagne Eric
Institute for Integrative Biology of the Cell (I2BC), Centre National de la Recherche Scientifique (CNRS), Commissariat Energie Atomique (CEA), Université Paris-Sud, Université Paris-Saclay, 91198 Gif-sur-Yvette, France.
Centre de Biologie du Développement (CBD), Centre de Biologie Intégrative (CBI) Université de Toulouse, CNRS, 31062 Toulouse, France.
Genes Dev. 2017 Sep 15;31(18):1880-1893. doi: 10.1101/gad.304543.117. Epub 2017 Oct 11.
Meiosis is the cellular program by which a diploid cell gives rise to haploid gametes for sexual reproduction. Meiotic progression depends on tight physical and functional coupling of recombination steps at the DNA level with specific organizational features of meiotic-prophase chromosomes. The present study reveals that every step of this coupling is mediated by a single molecule: Asy2/Mer2. We show that Mer2, identified so far only in budding and fission yeasts, is in fact evolutionarily conserved from fungi (Mer2/Rec15/Asy2/Bad42) to plants (PRD3/PAIR1) and mammals (IHO1). In yeasts, Mer2 mediates assembly of recombination-initiation complexes and double-strand breaks (DSBs). This role is conserved in the fungus However, functional analysis of 13 mutants and successive localization of Mer2 to axis, synaptonemal complex (SC), and chromatin revealed, in addition, three further important functions. First, after DSB formation, Mer2 is required for pairing by mediating homolog spatial juxtaposition, with implications for crossover (CO) patterning/interference. Second, Mer2 participates in the transfer/maintenance and release of recombination complexes to/from the SC central region. Third, after completion of recombination, potentially dependent on SUMOylation, Mer2 mediates global chromosome compaction and post-recombination chiasma development. Thus, beyond its role as a recombinosome-axis/SC linker molecule, Mer2 has important functions in relation to basic chromosome structure.
减数分裂是一种细胞程序,通过该程序,二倍体细胞产生用于有性生殖的单倍体配子。减数分裂的进程取决于DNA水平上重组步骤与减数分裂前期染色体的特定组织特征之间紧密的物理和功能耦合。本研究表明,这种耦合的每一步都是由单个分子介导的:Asy2/Mer2。我们发现,迄今仅在芽殖酵母和裂殖酵母中鉴定出的Mer2,实际上从真菌(Mer2/Rec15/Asy2/Bad42)到植物(PRD3/PAIR1)和哺乳动物(IHO1)在进化上是保守的。在酵母中,Mer2介导重组起始复合物的组装和双链断裂(DSB)。在真菌中这种作用是保守的。然而,对13个突变体的功能分析以及Mer2在轴、联会复合体(SC)和染色质上的连续定位还揭示了另外三个重要功能。首先,在DSB形成后,Mer2通过介导同源物的空间并列配对是必需的,这对交叉(CO)模式/干扰有影响。其次,Mer2参与重组复合物向SC中央区域的转移/维持以及从SC中央区域的释放。第三,在重组完成后,可能依赖于SUMO化,Mer2介导整体染色体压缩和重组后交叉的形成。因此,除了作为重组体 - 轴/SC连接分子的作用外,Mer2在基本染色体结构方面具有重要功能。