Sidorchuk Yuriy Vladimirovich, Deineko Elena Victorovna
Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences, Prospekt Lavrentyeva 10, Novosibirsk, 630090, Russian Federation.
Cell Biol Int. 2017 Jun;41(6):669-679. doi: 10.1002/cbin.10772. Epub 2017 May 2.
Microsporogenesis patterns of the polyploid (2n = 4x = 96) and diploid (2n = 2x = 48) Nicotiana tabacum L. (cv. Havana Petit line SR1) plants have been analyzed and compared. Four types of abnormal positions of the second-division spindles-tripolar, parallel, proximal, and fused-have been observed. Of these abnormalities, only tripolar (2.4%) and parallel (1.4%) spindles are observable in diploid plants. As for polyploids, the increased ploidy is accompanied by an increase in the incidence of tripolar (22.8%) and parallel (8.1%) spindle orientations and emergence of two remaining abnormalities (proximal and fused spindles, 3.3%). As has been shown, the spindle position abnormalities in diploid plants have no effect on the meiotic products, whereas both dyads and triads are detectable among the tetrads in polyploid plants. Analysis of cytoskeletal remodeling has allowed for the insight into the role of interzonal radial microtubule system in spindle positioning during the second division. The reason underlying the change in spindle positioning is disturbed polymerization-depolymerization processes and interdigitation of microtubule plus ends within the interzonal cytoskeleton system in late telophase I-interkinesis and prophase II. As has been demonstrated, fused second-division spindles are formed as a result of fused cytoskeletal structures in prophase-prometaphase II in the case when the nuclei are drawn abnormally close to one another.
对多倍体(2n = 4x = 96)和二倍体(2n = 2x = 48)烟草(品种哈瓦那小线SR1)植株的小孢子发生模式进行了分析和比较。观察到了第二次分裂纺锤体的四种异常位置——三极、平行、近端和融合。在这些异常中,二倍体植株中仅可观察到三极(2.4%)和平行(1.4%)纺锤体。对于多倍体而言,倍性增加伴随着三极(22.8%)和平行(8.1%)纺锤体取向发生率的增加以及另外两种异常(近端和融合纺锤体,3.3%)的出现。如已表明的,二倍体植株中的纺锤体位置异常对减数分裂产物没有影响,而在多倍体植株的四分体中可检测到二分体和三分体。细胞骨架重塑分析有助于深入了解间期径向微管系统在第二次分裂纺锤体定位中的作用。纺锤体定位变化的根本原因是在末期I - 分裂间期和前期II后期,区域间细胞骨架系统内微管正端的聚合 - 解聚过程和相互交错受到干扰。如已证明的,在细胞核异常靠近的情况下,融合的第二次分裂纺锤体是由于在前期 - 前中期II融合的细胞骨架结构形成的。