首页> 外文OA文献 >Assembly of chromatin fibers into metaphase chromosomes analyzed by transmission electron microscopy and scanning electron microscopy.
【2h】

Assembly of chromatin fibers into metaphase chromosomes analyzed by transmission electron microscopy and scanning electron microscopy.

机译:通过透射电子显微镜和扫描电子显微镜分析染色质纤维组装成中期染色体。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The higher-order assembly of the approximately 30 nm chromatin fibers into the characteristic morphology of HeLa mitotic chromosomes was investigated by electron microscopy. Transmission electron microscopy (TEM) of serial sections was applied to view the distribution of the DNA-histone-nonhistone fibers through the chromatid arms. Scanning electron microscopy (SEM) provided a complementary technique allowing the surface arrangement of the fibers to be observed. The approach with both procedures was to swell the chromosomes slightly, without extracting proteins, so that the densely-packed chromatin fibers were separated. The degree of expansion of the chromosomes was controlled by adjusting the concentration of divalent cations (Mg2+). With TEM, individual fibers could be resolved by decreasing the Mg2+ concentration to 1.0-1.5 mM. The predominant mode of fiber organization was seen to be radial for both longitudinal and transverse sections. Using SEM, surface protuberances with an average diameter of 69 nm became visible after the Mg2+ concentration was reduced to 1.5 mM. The knobby surface appearance was a variable feature, because the average diameter decreased when the divalent cation concentration was further reduced. The surface projections appear to represent the peripheral tips of radial chromatin loops. These TEM and SEM observations support a "radial loop" model for the organization of the chromatin fibers in metaphase chromosomes.
机译:通过电子显微镜研究了约30 nm染色质纤维到HeLa有丝分裂染色体特征形态的高阶组装。连续切片的透射电子显微镜(TEM)用于观察通过染色单体臂的DNA-组蛋白-非组蛋白纤维的分布。扫描电子显微镜(SEM)提供了一种补充技术,可以观察到纤维的表面排列。两种方法的方法都是在不提取蛋白质的情况下使染色体略微膨胀,从而分离出密集堆积的染色质纤维。通过调节二价阳离子(Mg2 +)的浓度来控制染色体的扩增程度。使用TEM,可以通过将Mg2 +浓度降低到1.0-1.5 mM来分离单个纤维。对于纵向和横向截面,纤维组织的主要模式被认为是径向的。使用SEM,在Mg2 +浓度降低到1.5 mM之后,可以看到平均直径为69 nm的表面突起。多角形表面外观是可变的特征,因为当进一步降低二价阳离子浓度时,平均直径减小。表面投影似乎代表了径向染色质环的外围尖端。这些TEM和SEM观察结果支持“径向环”模型,用于中期染色体中染色质纤维的组织。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号