Smolikov Sarit, Eizinger Andreas, Schild-Prufert Kristina, Hurlburt Allison, McDonald Kent, Engebrecht JoAnne, Villeneuve Anne M, Colaiácovo Mónica P
Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Genetics. 2007 Aug;176(4):2015-25. doi: 10.1534/genetics.107.072413. Epub 2007 Jun 11.
Synaptonemal complex (SC) formation must be regulated to occur only between aligned pairs of homologous chromosomes, ultimately ensuring proper chromosome segregation in meiosis. Here we identify SYP-3, a coiled-coil protein that is required for assembly of the central region of the SC and for restricting its loading to occur only in an appropriate context, forming structures that bridge the axes of paired meiotic chromosomes in Caenorhabditis elegans. We find that inappropriate loading of central region proteins interferes with homolog pairing, likely by triggering a premature change in chromosome configuration during early prophase that terminates the search for homologs. As a result, syp-3 mutants lack chiasmata and exhibit increased chromosome mis-segregation. Altogether, our studies lead us to propose that SYP-3 regulates synapsis along chromosomes, contributing to meiotic progression in early prophase.
联会复合体(SC)的形成必须受到调控,使其仅在同源染色体的配对排列之间发生,最终确保减数分裂过程中染色体的正确分离。在此,我们鉴定出SYP-3,一种卷曲螺旋蛋白,它是SC中央区域组装所必需的,并且能将其加载限制在适当的环境中,在秀丽隐杆线虫中形成连接配对减数分裂染色体轴的结构。我们发现,中央区域蛋白的不适当加载会干扰同源染色体配对,可能是通过在前期早期触发染色体构型的过早变化,从而终止对同源染色体的搜索。因此,syp-3突变体缺乏交叉,并表现出染色体错分离增加。总之,我们的研究使我们提出,SYP-3沿着染色体调节联会,有助于前期早期的减数分裂进程。