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使用抗乙酰化α-微管蛋白抗体鉴定紫外线剪切动粒纤维再生过程中微管聚合的位点。

Identifying the site of microtubule polymerization during regrowth of UV-sheared kinetochore fibres using antibodies against acetylated alpha-tubulin.

作者信息

Wilson P, Forer A

机构信息

Biology Department, York University, Ontario, Canada.

出版信息

Cell Biol Int Rep. 1989 Oct;13(10):823-32. doi: 10.1016/0309-1651(89)90123-9.

Abstract

Areas of reduced birefringence (ARBs) produced on chromosomal fibres of crane-fly spermatocyte spindles by ultraviolet microbeam irradiation move poleward. The ARB is due to the depolymerization of the microtubules in that area, and its poleward motion is due in part to the lengthening of that part of the kinetochore fibre which is left attached to the kinetochore after shearing the microtubules. We tested whether the lengthening of this fibre is due to the polymerization of microtubules at the growing edge of the ARB by staining growing fibres in irradiated spindles with antibodies to tubulin and to acetylated tubulin. We have previously argued that newly-polymerized kinetochore microtubules are not acetylated, whereas older kinetochore microtubules are (Wilson & Forer, 1989). Therefore we expected to see an absence of staining with antibodies to acetylated tubulin at the edge of the ARB if microtubules were polymerizing there. There is no absence of staining, however, which suggests that growth of the sheared microtubules does not occur at the ARB edge. Other possibilities are discussed.

摘要

经紫外线微束照射后,大蚊精母细胞纺锤体染色体纤维上产生的双折射降低区域(ARBs)会向极移动。ARBs是由于该区域微管的解聚,其向极运动部分归因于动粒纤维在微管切断后仍与动粒相连的部分的延长。我们通过用抗微管蛋白和抗乙酰化微管蛋白抗体对受照射纺锤体中生长的纤维进行染色,来测试这种纤维的延长是否是由于ARBs生长边缘微管的聚合。我们之前曾提出,新聚合的动粒微管未被乙酰化,而较老的动粒微管则被乙酰化(Wilson & Forer,1989)。因此,如果微管在ARBs边缘聚合,我们预期会看到抗乙酰化微管蛋白抗体在ARBs边缘无染色。然而,并非无染色,这表明切断的微管的生长并非发生在ARBs边缘。还讨论了其他可能性。

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