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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.

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。

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