Superresolution expansion microscopy reveals the three-dimensional organization of the Drosophila synaptonemal complex

被引:105
作者
Cahoon, Cori K. [1 ]
Yu, Zulin [1 ]
Wang, Yongfu [1 ]
Guo, Fengli [1 ]
Unruh, Jay R. [1 ]
Slaughter, Brian D. [1 ]
Hawley, R. Scott [1 ,2 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
[2] Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS 66160 USA
关键词
synaptonemal complex; expansion microscopy; meiosis; sister chromatids; structured illumination microscopy; CENTRAL REGION; CAENORHABDITIS-ELEGANS; FLUORESCENT PROTEINS; ELECTRON-MICROSCOPY; CENTRAL ELEMENT; BLAPS CRIBROSA; MEIOSIS; SPERMATOCYTES; MELANOGASTER; CHROMOSOMES;
D O I
10.1073/pnas.1705623114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The synaptonemal complex (SC), a structure highly conserved from yeast to mammals, assembles between homologous chromosomes and is essential for accurate chromosome segregation at the first meiotic division. In Drosophila melanogaster, many SC components and their general positions within the complex have been dissected through a combination of genetic analyses, superresolution microscopy, and electron microscopy. Although these studies provide a 2D understanding of SC structure in Drosophila, the inability to optically resolve the minute distances between proteins in the complex has precluded its 3D characterization. A recently described technology termed expansion microscopy (ExM) uniformly increases the size of a biological sample, thereby circumventing the limits of optical resolution. By adapting the ExM protocol to render it compatible with structured illumination microscopy, we can examine the 3D organization of several known Drosophila SC components. These data provide evidence that two layers of SC are assembled. We further speculate that each SC layer may connect two nonsister chromatids, and present a 3D model of the Drosophila SC based on these findings.
引用
收藏
页码:E6857 / E6866
页数:10
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