Suppr超能文献

荧光标记微管蛋白在海胆卵有丝分裂器中的重新分布及紫杉醇的作用

Redistribution of fluorescently labeled tubulin in the mitotic apparatus of sand dollar eggs and the effects of taxol.

作者信息

Hamaguchi Y, Toriyama M, Sakai H, Hiramoto Y

出版信息

Cell Struct Funct. 1987 Feb;12(1):43-52. doi: 10.1247/csf.12.43.

Abstract

Fluorescently labeled tubulin was quickly incorporated into the mitotic apparatus when injected into a live sand dollar egg. After a rectangular area (1.6 X 16 microns) of the mitotic spindle was photobleached at metaphase or anaphase by the irradiation of a laser microbeam, redistribution of fluorescence was almost complete within 30 sec. The photobleached area did not change in shape during the redistribution. During the period of redistribution, the bleached area moved slightly toward the near pole at metaphase and anaphase (means: 1.6 and 1.8 micron/min, respectively). These results indicate that redistribution was not due to the exchange of tubulin subunits only at the ends of microtubules but to their rapid exchange at sites along the microtubules in the bleached region. Furthermore, treadmilling of tubulin molecules along with the spindle microtubules possibly occurred at the rate of 1.6 micron/min at metaphase. Birefringence of the mitotic apparatus increased with a large increase in both the number and length of astral rays shortly after taxol was injected. However, the microtubules did not all seem to elongate at the same rate but appeared to become equalized in length. Chromosome movement stopped within 60 sec after the injection. Centrospheres became large and the labeled tubulin already incorporated into the centrospheres was excluded from the enlarged centrospheres. Shortly after the labeled tubulin was injected following the injection of taxol, it accumulated in the peripheral region of the centrospheres, suggesting that microtubules first assembled at this region. Fluorescently labeled tubulin in the mitotic apparatus in the egg after injection of taxol was redistributed much more slowly after photobleaching than in uninjected eggs.

摘要

当将荧光标记的微管蛋白注入活的海胆卵时,它会迅速整合到有丝分裂器中。在中期或后期,通过激光微束照射对有丝分裂纺锤体的一个矩形区域(1.6×16微米)进行光漂白后,荧光重新分布在30秒内几乎完成。在重新分布过程中,光漂白区域的形状没有改变。在重新分布期间,漂白区域在中期和后期向近极轻微移动(平均值分别为1.6和1.8微米/分钟)。这些结果表明,重新分布不是仅由于微管末端微管蛋白亚基的交换,而是由于它们在漂白区域沿微管位点的快速交换。此外,在中期,微管蛋白分子沿纺锤体微管的踏车运动可能以1.6微米/分钟的速度发生。注射紫杉醇后不久,有丝分裂器的双折射随着星体射线数量和长度的大幅增加而增加。然而,微管似乎并非都以相同的速度伸长,而是长度趋于相等。注射后60秒内染色体运动停止。中心球变大,已经整合到中心球中的标记微管蛋白被排除在扩大的中心球之外。在注射紫杉醇后不久注射标记微管蛋白后,它聚集在中心球的周边区域,这表明微管首先在该区域组装。注射紫杉醇后,卵中有丝分裂器中的荧光标记微管蛋白在光漂白后的重新分布比未注射的卵慢得多。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验