Bähler J, Wyler T, Loidl J, Kohli J
Institute of General Microbiology, University of Bern, Switzerland.
J Cell Biol. 1993 Apr;121(2):241-56. doi: 10.1083/jcb.121.2.241.
Earlier results from sectioned nuclei indicating that Schizosaccharomyces pombe does not develop a classical tripartite synaptonemal complex (SC) during meiotic prophase are confirmed by spreading of whole nuclei. The linear elements appearing during prophase I resemble the axial cores (SC precursors) of other organisms. The number of linear elements in haploid, diploid, and tetraploid strains is always higher than the chromosome number, implying that they are not formed continuously along the chromosomes. Time course experiments reveal that the elements appear after DNA replication and form networks and bundles. Later they separate and approximately 24 individual elements with a total length of 34 microns are observed before degradation and meiotic divisions. Parallel staining of DNA reveals changes in nuclear shape during meiotic prophase. Strains with a mei4 mutation are blocked at a late prophase stage. In serial sections we additionally observed a constant arrangement of the spindle pole body, the nucleolus, and the presumptive centromere cluster. Thus, S. pombe manages to recombine and segregate its chromosomes without SC. This might correlate with the absence of crossover interference. We propose a mechanism for chromosome pairing with initial recognition of the homologs at the centromeres and suggest functions of the linear elements in preparation of the chromosomes for meiosis I disjunction. With the spreading technique combined genetic, molecular, and cytological approaches become feasible in S. pombe. This provides an opportunity to study essential meiotic functions in the absence of SCs which may help to clarify the significance of the SC and its components for meiotic chromosome structure and function.
对细胞核进行切片的早期结果表明,粟酒裂殖酵母在减数分裂前期不会形成典型的三联体联会复合体(SC),这一结果通过对整个细胞核的铺展得到了证实。减数分裂前期I出现的线性元件类似于其他生物体的轴状核心(SC前体)。单倍体、二倍体和四倍体菌株中的线性元件数量总是高于染色体数量,这意味着它们不是沿着染色体连续形成的。时间进程实验表明,这些元件在DNA复制后出现,并形成网络和束状结构。随后它们分离,在降解和减数分裂之前观察到大约24个单个元件,总长度为34微米。对DNA的平行染色揭示了减数分裂前期细胞核形状的变化。具有mei4突变的菌株在减数分裂前期后期受阻。在连续切片中,我们还观察到纺锤体极体、核仁和假定的着丝粒簇的恒定排列。因此,粟酒裂殖酵母能够在没有SC的情况下重组和分离其染色体。这可能与没有交叉干扰有关。我们提出了一种染色体配对机制,即同源染色体在着丝粒处进行初始识别,并提出了线性元件在为减数分裂I分离准备染色体过程中的功能。通过铺展技术,遗传学、分子学和细胞学方法在粟酒裂殖酵母中变得可行。这为在没有SC的情况下研究减数分裂的基本功能提供了机会,这可能有助于阐明SC及其组件对减数分裂染色体结构和功能的重要性。