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多头绒泡菌变形虫分离的微管组织中心引发的微管成核作用。

Microtubule nucleation by the isolated microtubule-organizing centre of Physarum polycephalum myxamoebae.

作者信息

Roobol A, Havercroft J C, Gull K

出版信息

J Cell Sci. 1982 Jun;55:365-81. doi: 10.1242/jcs.55.1.365.

Abstract

The nucleus--centrosome complex from Physarum polycephalum myxamoebae has been purified. The complex contained the centriole pair and pericentriolar material in association with the nucleus. Apart from some unusually stable microtubules, which appeared to be involved in maintaining the nucleus-centrosome association, endogenous microtubule arrays had been stripped from the complex during isolation. When the nucleus--centrosome complex was incubated with purified brain or myxamoebal tubulins the growth of 45-70 microtubules was initiated onto the pericentriolar material. The number and length of the nucleated microtubules was proportional to the tubulin concentration. Pretreatment of the nucleus--centrosome complex with DNase 1, RNase A, antitubulin antibody and anticentriolar antibody did not affect pericentriolar nucleation capacity, although pretreatment with DNase 1 did expose perinuclear nucleation sites that had a much lower minimal tubulin concentration for assembly than the pericentriolar site. After pretreatment with trypsin pericentriolar material and nucleation were destroyed, and microtubule elongation occurred directly onto the centriole microtubules.

摘要

多头绒泡菌变形体的细胞核 - 中心体复合体已被纯化。该复合体包含与细胞核相关联的中心粒对和中心粒周围物质。除了一些似乎参与维持细胞核 - 中心体关联的异常稳定的微管外,内源性微管阵列在分离过程中已从复合体中去除。当细胞核 - 中心体复合体与纯化的脑微管蛋白或变形体微管蛋白一起孵育时,45 - 70根微管开始在中心粒周围物质上生长。成核微管的数量和长度与微管蛋白浓度成正比。用DNA酶1、RNA酶A、抗微管蛋白抗体和抗中心粒抗体对细胞核 - 中心体复合体进行预处理不会影响中心粒周围的成核能力,尽管用DNA酶1预处理确实暴露了核周成核位点,该位点组装所需的最低微管蛋白浓度比中心粒周围位点低得多。用胰蛋白酶预处理后,中心粒周围物质和成核被破坏,微管直接在中心粒微管上延伸。

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