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Programmed synthesis of tubulin for the flagella that develop during cell differentiation in Naegleria gruberi.在格氏变形虫细胞分化过程中,为发育的鞭毛进行微管蛋白的程序性合成。
Proc Natl Acad Sci U S A. 1974 Jul;71(7):2877-81. doi: 10.1073/pnas.71.7.2877.
2
Programmed synthesis of flagellar tubulin during cell differentiation in Naegleria.嗜脑阿米巴中细胞分化过程中鞭毛微管蛋白的程序性合成。
Ann N Y Acad Sci. 1975 Jun 30;253:318-32. doi: 10.1111/j.1749-6632.1975.tb19210.x.
3
Purification and properties of flagellar outer doublet tubulin from Naegleria gruberi and a radioimmune assay for tubulin.格氏耐格里阿米巴鞭毛外双联体微管蛋白的纯化及性质与微管蛋白的放射免疫测定
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4
Transcriptional regulation of coordinate changes in flagellar mRNAs during differentiation of Naegleria gruberi amebae into flagellates.在格氏耐格里变形虫分化为鞭毛虫的过程中,鞭毛mRNA协同变化的转录调控。
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Macromolecular syntheses during the quick-change act of Naegleria.纳氏虫快速变化过程中的大分子合成。
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7
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9
Tubulin biosynthesis in the developmental cycle of a parasitic protozoan, Leishmania mexicana: changes during differentiation of motile and nonmotile stages.墨西哥利什曼原虫(一种寄生原生动物)发育周期中的微管蛋白生物合成:活动期和非活动期分化过程中的变化
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Tandem arrangement of tubulin genes in the protozoan parasite Leishmania enriettii.原生动物寄生虫恩氏利什曼原虫微管蛋白基因的串联排列。
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MOLECULAR FACETS OF MITOTIC REGULATION, I. SYNTHESIS OF THYMIDINE KINASE.有丝分裂调控的分子层面,I. 胸苷激酶的合成
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Flagellar elongation and shortening in Chlamydomonas. The use of cycloheximide and colchicine to study the synthesis and assembly of flagellar proteins.衣藻中鞭毛的伸长与缩短。使用放线菌酮和秋水仙碱研究鞭毛蛋白的合成与组装。
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Chemical and structural differences between cilia and flagella from the lamellibranch mollusc, Aequipecten irradians.双壳贝类软体动物海湾扇贝的纤毛和鞭毛之间的化学和结构差异。
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在格氏变形虫细胞分化过程中,为发育的鞭毛进行微管蛋白的程序性合成。

Programmed synthesis of tubulin for the flagella that develop during cell differentiation in Naegleria gruberi.

作者信息

Kowit J D, Fulton C

出版信息

Proc Natl Acad Sci U S A. 1974 Jul;71(7):2877-81. doi: 10.1073/pnas.71.7.2877.

DOI:10.1073/pnas.71.7.2877
PMID:4604968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC388575/
Abstract

Amebae of Naegleria gruberi differentiate into flagellates when transferred from growth medium to nonnutrient buffer. Experiments were performed to determine whether the tubulin that forms the flagellar microtubules pre-exists in amebae or is synthesized during differentiation. Amebae prelabeled uniformly with [(35)S]methionine were allowed to differentiate in the presence and in the absence of exogenous unlabeled methionine. In the presence of unlabeled methionine the flagellar tubulin contained only 30% as much [(35)S]methionine as in its absence. Thus at least 70% of the tubulin was synthesized de novo. Isotope dilution and pulse experiments showed that flagellar tubulin synthesis began one-third of the way through differentiation, before any morphological change had occurred. Flagellar tubulin antigen, as measured using a specific antiserum, also began to increase one-third of the way through differentiation and increased 35- to 55-fold during the course of differentiation. These experiments demonstrate that most if not all of the flagellar tubulin is synthesized de novo during differentiation.

摘要

格氏耐格里变形虫从生长培养基转移到无营养缓冲液中时会分化为鞭毛虫。进行了实验以确定形成鞭毛微管的微管蛋白在变形虫中是否预先存在,还是在分化过程中合成。用[(35)S]甲硫氨酸均匀预标记的变形虫在有和没有外源性未标记甲硫氨酸的情况下进行分化。在有未标记甲硫氨酸存在的情况下,鞭毛微管蛋白所含的[(35)S]甲硫氨酸仅为不存在时的30%。因此,至少70%的微管蛋白是重新合成的。同位素稀释和脉冲实验表明,鞭毛微管蛋白的合成在分化进行到三分之一时开始,此时尚未发生任何形态变化。使用特异性抗血清测定,鞭毛微管蛋白抗原在分化进行到三分之一时也开始增加,并且在分化过程中增加了35至55倍。这些实验表明,在分化过程中,大部分(如果不是全部)鞭毛微管蛋白是重新合成的。