Lin H P, Ault J G, Church K
Chromosoma. 1981;83(4):507-21. doi: 10.1007/BF00328276.
Individual bivalents or chromosomes have been identified in Drosophila melanogaster spermatocytes at metaphase I, anaphase I, metaphase II and anaphase II in electron micrographs of serial sections. Identification was based on a combination of chromosome volume analysis, bivalent topology, and kinetochore position. - Kinetochore microtubule numbers have been obtained for the identified chromosomes at all four meiotic stages. Average numbers in D. melanogaster are relatively low compared to reported numbers of other higher eukaryotes. There is no differences in kinetochore microtubule numbers within a stage despite a large (approximately tenfold) difference in chromosome volume between the largest and the smallest chromosome. A comparison between the two meiotic metaphases (metaphase I and metaphase II) reveals that metaphase I kinetochores possess twice as many microtubules as metaphase II kinetochores. - Other microtubules in addition to those that end on or penetrate the kinetochore are found in the vicinity of the kinetochore. These microtubules penetrate the chromosome rather than the kinetochore proper and are more numerous at metaphase I than at the other division stages.
在黑腹果蝇精母细胞减数分裂的中期 I、后期 I、中期 II 和后期 II,通过连续切片的电子显微镜照片已识别出单个二价体或染色体。识别基于染色体体积分析、二价体拓扑结构和动粒位置的综合判断。已获得所有四个减数分裂阶段中已识别染色体的动粒微管数量。与其他高等真核生物报道的数量相比,黑腹果蝇的平均数量相对较低。尽管最大和最小染色体的体积存在很大差异(约十倍),但同一阶段内动粒微管数量并无差异。两个减数分裂中期(中期 I 和中期 II)的比较显示,中期 I 动粒的微管数量是中期 II 动粒的两倍。除了那些终止于或穿透动粒的微管外,在动粒附近还发现了其他微管。这些微管穿透染色体而非动粒本身,并且在中期 I 比在其他分裂阶段更多。