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海胆胚胎中的量子化微管蛋白合成与纤毛长度

Quantal tektin synthesis and ciliary length in sea-urchin embryos.

作者信息

Stephens R E

机构信息

Marine Biological Laboratory, Woods Hole, MA 02543.

出版信息

J Cell Sci. 1989 Mar;92 ( Pt 3):403-13. doi: 10.1242/jcs.92.3.403.

Abstract

Previous work using pulse-chase labelling of embryos from the sea-urchin Strongylocentrotus droebachiensis during ciliogenesis, regeneration or steady-state maintenance and elongation showed that a ciliary outer doublet microtubule-associated protein, originally termed component-20, was synthesized in a fixed or quantal amount. This suggested that the limited synthesis of component-20 might limit ciliary length, since the embryo has a large pool of most other ciliary components. Labelling experiments with S. purpuratus embryos now confirm quantal synthesis of component-20, while antibodies to S. purpuratus sperm flagellar tektins identify component-20 as the ciliary equivalent of the flagellar 55 x 10(3) Mr tektin, tektin A. Sequential pulse-chase labelling at various times prior to isolation of cilia proves that the high specific activity of this protein truly reflects de novo synthesis of a structurally stable protein and not rapid protein turnover. Embryos may be animalized by growth in the presence of zinc ions, resulting in cilia averaging nearly twice the normal 20 microns length. When these embryos are pulse-chase labelled during ciliary growth and elongation, labelling of tektin A is proportional to the greater ciliary length, as is the pool of labelled but unincorporated tektins and other minor proteins. Deciliated animalized and control embryos, pulse-chase labelled during their identical phases of ciliary regeneration, incorporate labelled tektin A to the same extent and have similar pools of unincorporated proteins. The correlation of enhanced tektin A synthesis with increased ciliary length and the coincidence of tektin A synthesis with ciliary elongation are observations consistent with the hypothesis that tektin A is a ciliary length-limiting structural element.

摘要

此前,对来自大西洋海胆(Strongylocentrotus droebachiensis)的胚胎在纤毛发生、再生或稳态维持与延长过程中进行脉冲追踪标记的研究表明,一种最初被称为组分20的纤毛外双联微管相关蛋白是以固定或定量的方式合成的。这表明组分20的有限合成可能限制了纤毛长度,因为胚胎中大多数其他纤毛组分都有大量储备。现在,对紫球海胆(S. purpuratus)胚胎的标记实验证实了组分20的定量合成,而针对紫球海胆精子鞭毛轴纤丝蛋白的抗体将组分20鉴定为鞭毛55×10³ Mr轴纤丝蛋白(轴纤丝蛋白A)的纤毛对应物。在分离纤毛之前的不同时间进行连续脉冲追踪标记证明,这种蛋白质的高比活性真正反映了一种结构稳定的蛋白质的从头合成,而不是快速的蛋白质周转。胚胎在锌离子存在的情况下生长可能会发生动物化,导致纤毛平均长度几乎是正常的20微米长度的两倍。当这些胚胎在纤毛生长和延长过程中进行脉冲追踪标记时,轴纤丝蛋白A的标记与更长的纤毛长度成比例,标记但未掺入的轴纤丝蛋白和其他次要蛋白质的储备也是如此。在纤毛再生的相同阶段对去纤毛的动物化胚胎和对照胚胎进行脉冲追踪标记,它们掺入标记轴纤丝蛋白A的程度相同,未掺入蛋白质的储备也相似。轴纤丝蛋白A合成增强与纤毛长度增加之间的相关性以及轴纤丝蛋白A合成与纤毛延长的一致性,这些观察结果与轴纤丝蛋白A是一种限制纤毛长度的结构元件这一假设相符。

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