Anderson Lorinda K, Stack Stephen M
Department of Biology, Colorado State University, Fort Collins, CO, USA.
Methods Mol Biol. 2013;990:147-58. doi: 10.1007/978-1-62703-333-6_15.
Recombination nodules (RNs) are associated with synaptonemal complexes (SCs) during early prophase I of meiosis. RNs are too small to be resolved by light microscopy and can be observed directly only by electron microscopy. The patterns of RNs on SCs can be analyzed using three-dimensional reconstructions of nuclei using serial thin sections, but this method is time consuming and technically difficult. In contrast, spreads of SCs are in one plane so all RNs in each set can be visualized simultaneously, and the patterns of both early and late nodules (ENs and LNs) can be analyzed far more easily than using sections. Here, we describe methods for preparing spreads of SCs and RNs from tomato primary microsporocytes on plastic-coated slides for visualization by transmission electron microscopy (TEM).
重组小结(RNs)在减数分裂前期I早期与联会复合体(SCs)相关联。RNs太小,无法通过光学显微镜分辨,只能通过电子显微镜直接观察。使用连续薄切片对细胞核进行三维重建可以分析SCs上RNs的模式,但这种方法耗时且技术难度大。相比之下,SCs的铺展在一个平面上,因此每组中的所有RNs可以同时可视化,并且早期和晚期小结(ENs和LNs)的模式比使用切片更容易分析。在这里,我们描述了从番茄初级小孢子母细胞制备SCs和RNs铺展物的方法,这些铺展物置于涂有塑料的载玻片上,用于透射电子显微镜(TEM)观察。