Brown R C, Lemmon B E
Department of Biology, University of Louisiana-Lafayette, Lafayette, LA 70504, USA.
J Plant Res. 2005 Apr;118(2):121-8. doi: 10.1007/s10265-005-0199-1. Epub 2005 Mar 15.
This is the first report on gamma-tubulin and microtubule arrays during microsporogenesis in a gymnosperm. Meiosis in Ginkgo biloba is polyplastidic, as is typical of the spermatophyte clade, and microtubule arrays are organized at various sites during meiosis and cytokinesis. In early prophase, a cluster of gamma-tubulin globules occurs in the central cytoplasm adjacent to the off-center nucleus. These globules diminish in size and spread over the surface of the nucleus. A system of microtubules focused on the gamma-tubulin forms a reticulate pattern in the cytoplasm. As the nucleus migrates to the center of the microsporocyte, gamma-tubulin becomes concentrated at several sites adjacent to the nuclear envelope. Microtubules organized at these foci of gamma-tubulin give rise to a multipolar prophase spindle. By metaphase I, the spindle has matured into a distinctly bipolar structure with pointed poles. In both first and second meiosis, gamma-tubulin becomes distributed throughout the metaphase spindles, but becomes distinctly polar again in anaphase. In telophase I, gamma-tubulin moves from polar regions to the proximal surface of chromosome groups/nuclei where interzonal microtubules are organized. No cell wall is deposited and the interzonal microtubules embrace a plate of organelles between the two nuclear cytoplasmic domains (NCDs) of the dyad. Following second meiosis, phragmoplasts that form between sister and non-sister nuclei fuse to form a complex six-sided structure that directs simultaneous cytokinesis. Gamma-tubulin becomes associated with nuclei after both meiotic divisions and is especially conspicuous in the distal hemisphere of each young microspore where an unusual encircling system of cortical microtubules develops.
这是关于裸子植物小孢子发生过程中γ-微管蛋白和微管阵列的首篇报道。银杏的减数分裂具有多质体特征,这是种子植物分支的典型特征,并且在减数分裂和胞质分裂过程中,微管阵列在不同位点形成。在前期早期,一团γ-微管蛋白小球出现在偏离中心的细胞核附近的中央细胞质中。这些小球体积减小并扩散到细胞核表面。聚焦于γ-微管蛋白的微管系统在细胞质中形成网状模式。随着细胞核迁移到小孢子母细胞的中心,γ-微管蛋白集中在核膜附近的几个位点。在这些γ-微管蛋白焦点处组织形成的微管产生一个多极前期纺锤体。到中期I时,纺锤体成熟为具有尖极的明显双极结构。在第一次和第二次减数分裂中,γ-微管蛋白都分布在中期纺锤体中,但在后期又再次明显极化。在末期I,γ-微管蛋白从极区移动到染色体组/细胞核的近端表面,在那里形成间区微管。没有细胞壁沉积,间区微管在二分体的两个核细胞质区域(NCDs)之间包围着一层细胞器。第二次减数分裂后,在姐妹细胞核和非姐妹细胞核之间形成的成膜体融合形成一个复杂的六边形结构,引导同时进行的胞质分裂。在两次减数分裂后,γ-微管蛋白都与细胞核相关联,并且在每个年轻小孢子的远端半球特别明显,在那里形成了一个不寻常的环绕皮质微管系统。