Karadzhian B P
Tsitologiia. 1977;19(12):1327-32.
Six stages can be distinguished in the micronuclear first maturation division prophase of D. nasutum. Nucleolus-like structures of fibrillar nature, connected with micronuclear chromosomes seem to develop at the late leptotene. At zygotene-pachytene, the chromosomes condense, forming irregular loops. This coincides with formation of classically structured synaptinemal complexes in the micronuclei. At diplotene-diakinesis, chromosomal bivalents are uniformly scattered throughout the micronucleus. They aggregate into a net equatorial plate in the first division metaphase; chromosomes show prominent kinetochores with attached chromosomal microtubule bundles. The second maturation division starts immediately after the completion of the first division and is morphologically similar to agamic mitosis of the micronuclei of D. nasutum. During the 2th maturation division prophase, the compact chromosomes form a dense group and show no spreading inside the nucleus. They are interspaced by an amorphous material being possibly involved in the formation of spindle microtubules. The telophase spindle of the 2nd division likely as that of the Ist division divides into three parts, the two daughter nuclei and the separation spindle containing a material of depolymerized microtubules. Only one of the 2nd division derivatives enters the third maturation division. A short telophasic third division spindle is perpendicular to the surface of the contact between the conjugants and produces two pronuclei. The envelopes of the daughter micronuclei are formed from parts of the original nuclear envelope surrounding the entire spindle.
在纳氏果蝇微核第一次成熟分裂前期可区分出六个阶段。在细线期后期,似乎会形成与微核染色体相连的纤维状核仁样结构。在偶线期-粗线期,染色体浓缩,形成不规则环。这与微核中经典结构的联会复合体的形成同时发生。在双线期-终变期,染色体二价体均匀地散布在整个微核中。它们在第一次分裂中期聚集成一个赤道板网;染色体显示出带有附着的染色体微管束的明显着丝粒。第二次成熟分裂在第一次分裂完成后立即开始,在形态上类似于纳氏果蝇微核的无融合有丝分裂。在第二次成熟分裂前期,紧密的染色体形成一个密集的群体,在细胞核内没有散开。它们被一种可能参与纺锤体微管形成的无定形物质隔开。第二次分裂的末期纺锤体可能与第一次分裂的纺锤体一样分成三部分,即两个子核和含有解聚微管物质的分离纺锤体。第二次分裂的衍生物中只有一个进入第三次成熟分裂。一个短的末期第三次分裂纺锤体垂直于接合体之间接触的表面,并产生两个原核。子微核的包膜由围绕整个纺锤体的原始核包膜的部分形成。