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对动粒进行紫外线微束照射后动粒微管的电子显微镜和免疫化学分析。

Electron-microscopic and immunochemical analysis of kinetochore microtubules after ultraviolet microbeam irradiation of kinetochores.

作者信息

Swedak J A, Leggiadro C, Forer A

机构信息

Biology Department, York University, North York, Ontario, Canada.

出版信息

J Cell Sci. 1991 Oct;100 ( Pt 2):269-77. doi: 10.1242/jcs.100.2.269.

Abstract

We used an ultraviolet microbeam to irradiate kinetochores of chromosomes in crane-fly spermatocytes. We used one of two doses, low (0.106 erg microns-2) or high (0.301 erg microns-2), and then studied the microtubules in those spindles using electron microscopy or immunofluorescence microscopy. After irradiation with low doses microtubules are present as usual, with normal fluorescence and in normal numbers. After irradiation with high doses microtubules are no longer associated with the irradiated kinetochore. After irradiation with either dose, non-kinetochore microtubules are in smaller numbers in the irradiated half-spindle than in the non-irradiated half-spindle or in non-irradiated cells. Since irradiation with low doses alters interchromosomal 'signals', but microtubules remain attached to the kinetochore, we argue that low doses of ultraviolet light damage a signal-related function of kinetochores without altering the ability of the kinetochores to bind microtubules.

摘要

我们使用紫外线微束照射大蚊精母细胞中染色体的动粒。我们采用了两种剂量中的一种,低剂量(0.106尔格·微米-2)或高剂量(0.301尔格·微米-2),然后使用电子显微镜或免疫荧光显微镜研究这些纺锤体中的微管。低剂量照射后,微管如往常一样存在,具有正常的荧光且数量正常。高剂量照射后,微管不再与受照射的动粒相关联。无论采用哪种剂量照射,受照射半纺锤体中的非动粒微管数量都比未受照射的半纺锤体或未受照射细胞中的少。由于低剂量照射会改变染色体间的“信号”,但微管仍附着在动粒上,我们认为低剂量紫外线会损害动粒的信号相关功能,而不会改变动粒结合微管的能力。

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