Department of Biology, Faculty of Science, Tokyo Metropolitan University, Fukazawa, 158, Tokyo, Japan.
Planta. 1991 Feb;183(3):391-8. doi: 10.1007/BF00197738.
Protonemata of Adiantum capillus-veneris L., grown in red light and consisting of a single elongate cell, were centrifuged at various times after or just before the induction of synchronous cell division by irradiation with blue light (BL), and formation and location of preprophase bands (PPBs) of microtubules (MTs) were observed by immunofluorescence microscopy. The cells divided approx. 14-20 h after the onset of BL irradiation, irrespective of the timing of centrifugation. Basipetal centrifugation caused basipetal displacement (about 100 μm) of the nucleus. The nucleus did not return to its original position and cell division occurred at the new nuclear position. A PPB was formed in the region of the displaced nucleus except in some cells which presumably had been centrifuged just before cell division. Microtubule behavior in the apical region, where cell division occurred in non-centrifuged cells, depended on the time of centrifugation relative to the cell cycle. When protonemata were centrifuged before PPB formation, no PPB was formed in the apical region of most cells but, in some cells, another MT band indistinguishable from a PPB (we consider it PPB) was formed at this site after the displacement of the nucleus. When protonemata were centrifuged during or after PPB formation, the PPB, which had already formed in the apical region, did not disappear until the sedimented nucleus entered telophase or early interphase, while a new PPB was formed in most cells in the region of the displaced nucleus. These cells had thus two PPBs: one in the apical region, and another in the region where the displaced nucleus was located. Double centrifugation to displace the nucleus twice showed that once a PPB formed, irrespective of its intracellular position, it remained after the displacement of the nucleus. However, no PPBs were observed in the region where the nucleus was located after the first centrifugation if the nucleus was again displaced before a PPB had formed in this region. The positioning of the cell plate was also examined. When centrifugation was performed just before cell division, PPB formation around the displaced nucleus decreased and oblique cell plates were observed at an increased frequency. In conclusion, preprophase nuclei may have the ability to induce PPB formation in the neighboring cell cortex, and PPBs, in turn, may have a role in governing the orientation of cell plates.
铁线蕨原叶体在红光中生长,由一个单一的细长细胞组成,在受到蓝光(BL)照射诱导同步细胞分裂之前或之后的不同时间进行离心,通过免疫荧光显微镜观察微管(MT)的前期带(PPB)的形成和位置。细胞在 BL 照射开始后约 14-20 小时分裂,与离心时间无关。向基离心导致核的向基位移(约 100 μm)。核没有回到原来的位置,细胞在新的核位置分裂。在位移核的区域形成一个 PPB,但在一些可能在细胞分裂前刚刚离心的细胞中没有形成。在未离心细胞中发生细胞分裂的顶端区域,微管行为取决于相对于细胞周期的离心时间。当原叶体在 PPB 形成之前离心时,大多数细胞的顶端区域没有形成 PPB,但在一些细胞中,另一个与 PPB 不可区分的微管带(我们认为它是 PPB)在核位移后在此处形成。当原叶体在 PPB 形成期间或之后离心时,已经在顶端区域形成的 PPB 不会消失,直到沉降核进入末期或早期间期中,而在位移核所在区域的大多数细胞中形成了一个新的 PPB。这些细胞因此有两个 PPB:一个在顶端区域,另一个在位移核所在的区域。两次离心以两次位移核表明,一旦形成了 PPB,无论其在细胞内的位置如何,核位移后它都会保留下来。然而,如果在该区域形成 PPB 之前再次位移核,则在第一次离心后不会在核所在的区域观察到 PPB。细胞板的定位也进行了检查。当在细胞分裂前进行离心时,围绕位移核的 PPB 形成减少,并且观察到斜细胞板的频率增加。总之,前期核可能具有在邻近的细胞皮层中诱导 PPB 形成的能力,而 PPB 反过来又可能在控制细胞板的取向中发挥作用。