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烟草细胞中的翻译后修饰与多种微管蛋白异构体

Post-translational modifications and multiple tubulin isoforms in Nicotiana tabacum L. cells.

作者信息

Smertenko A, Blume Y, Viklický V, Opatrný Z, Dráber P

机构信息

Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Czech Republic.

出版信息

Planta. 1997;201(3):349-58. doi: 10.1007/s004250050077.

Abstract

Distribution of post-translationally modified tubulins in cells of Nicotiana tabacum L. was analysed using a panel of specific antibodies. Polyglutamylated, tyrosinated, nontyrosinated, acetylated and delta 2-tubulin variants were detected on alpha-tubulin subunits; polyglutamylation was also found on beta-tubulin subunits. Modified tubulins were detected by immunofluorescence microscopy in interphase microtubules, preprophase bands, mitotic spindles as well as in phragmoplasts. They were, however, located differently in the various microtubule structures. The antibodies against tyrosinated, acetylated and polyglutamylated tubulins gave uniform staining along all microtubules, while antibodies against nontyrosinated and delta 2-tubulin provided dot-like staining of interphase microtubules. Additionally, immunoreactivity of antibodies against acetylated and delta 2-tubulins was strong in the pole regions of mitotic spindles. High-resolution isoelectric focusing revealed 22 tubulin charge variants in N. tabacum suspension cells. Immunoblotting with antibodies TU-01 and TU-06 against conserved antigenic determinants of alpha- and beta-tubulin molecules, respectively, revealed that 11 isoforms belonged to the alpha-subunit and 11 isoforms to the beta-subunit. Whereas antibodies against polyglutamylated, tyrosinated and acetylated tubulins reacted with several alpha-tubulin isoforms, antibodies against nontyrosinated and delta 2-tubulin reacted with only one. The combined data demonstrate that plant tubulin is extensively post-translationally modified and that these modifications participate in the generation of plant tubulin polymorphism.

摘要

利用一组特异性抗体分析了烟草细胞中翻译后修饰微管蛋白的分布情况。在α-微管蛋白亚基上检测到了多聚谷氨酰化、酪氨酰化、非酪氨酰化、乙酰化和δ2-微管蛋白变体;在β-微管蛋白亚基上也发现了多聚谷氨酰化。通过免疫荧光显微镜在间期微管、前期带、有丝分裂纺锤体以及成膜体中检测到了修饰的微管蛋白。然而,它们在各种微管结构中的定位有所不同。抗酪氨酰化、乙酰化和多聚谷氨酰化微管蛋白的抗体沿着所有微管产生均匀染色,而抗非酪氨酰化和δ2-微管蛋白的抗体对间期微管产生点状染色。此外,抗乙酰化和δ2-微管蛋白的抗体在有丝分裂纺锤体的极区免疫反应强烈。高分辨率等电聚焦显示烟草悬浮细胞中有22种微管蛋白电荷变体。分别用针对α-和β-微管蛋白分子保守抗原决定簇的抗体TU-01和TU-06进行免疫印迹分析,结果显示11种异构体属于α-亚基,11种异构体属于β-亚基。抗多聚谷氨酰化、酪氨酰化和乙酰化微管蛋白的抗体与几种α-微管蛋白异构体发生反应,而抗非酪氨酰化和δ2-微管蛋白的抗体只与一种异构体发生反应。综合数据表明植物微管蛋白在翻译后被广泛修饰,并且这些修饰参与了植物微管蛋白多态性的产生。

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