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海胆胚胎纤毛中的微管蛋白和轴丝纤维蛋白:周转和再生过程中蛋白质整合的途径

Tubulin and tektin in sea urchin embryonic cilia: pathways of protein incorporation during turnover and regeneration.

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. 1994 Feb;107 ( Pt 2):683-92.

PMID:8207090
Abstract

Axonemal precursor tubulin is the major protein component of the detergent-soluble membrane/matrix fraction of sea urchin embryonic cilia. Its unusual abundance may reflect the rapid turnover of these cilia, a process that is further documented here. However, whether during induced regeneration or normal turnover and growth, most other newly synthesized axonemal proteins are not detectable in the membrane/matrix fraction, raising the question of how non-tubulin precursors transit the growing cilium to the distal tip where assembly is generally thought to occur. Three potential explanations were considered: (1) the assembly of these components is proximal; (2) their relative concentration is too low to detect; or (3) tubulin alone is conveyed via a membrane/matrix pathway while most other axonemal proteins are transported in association with the axoneme. Light microscope autoradiography of axonemes pulse-chase labeled with [3H]leucine showed relatively uniform labeling, with no evidence for proximal incorporation. Fully grown cilia and cilia at early stages of regeneration were isolated from labeled embryos, fractionated into membrane/matrix, axonemal tubulin and architectural remnant components, and their labeled protein compositions were compared. Heavily labeled axonemal proteins, most notably the integral microtubule doublet component tektin-A, were not detected in the membrane/matrix fraction of emerging cilia, even though nearly half of the total ciliary tubulin appeared in that fraction, arguing against membrane-associated or soluble matrix transit for the architectural proteins at low concentrations. However, after thermal fractionation of axonemes from growing cilia, labeled proteins characteristic of the architectural remnant dominated the solubilized microtubule fraction, supporting axoneme-associated transport of the non-tubulin proteins during growth, in contrast to a membrane/matrix pathway for tubulin.

摘要

轴丝前体微管蛋白是海胆胚胎纤毛去污剂可溶膜/基质部分的主要蛋白质成分。其异常丰富可能反映了这些纤毛的快速周转,本文进一步记录了这一过程。然而,无论是在诱导再生过程中还是在正常周转和生长过程中,大多数其他新合成的轴丝蛋白在膜/基质部分中都无法检测到,这就引发了一个问题,即非微管蛋白前体如何通过生长中的纤毛转运到通常认为发生组装的远端尖端。考虑了三种可能的解释:(1) 这些成分的组装是近端的;(2) 它们的相对浓度太低而无法检测到;或者 (3) 仅微管蛋白通过膜/基质途径运输,而大多数其他轴丝蛋白与轴丝相关运输。用 [3H] 亮氨酸进行脉冲追踪标记的轴丝的光学显微镜放射自显影显示标记相对均匀,没有近端掺入的证据。从标记的胚胎中分离出完全生长的纤毛和再生早期的纤毛,将其分离为膜/基质、轴丝微管蛋白和结构残余成分,并比较它们的标记蛋白质组成。即使几乎一半的总纤毛微管蛋白出现在该部分中,在新生纤毛的膜/基质部分中也未检测到大量标记的轴丝蛋白,最显著的是完整微管双联体成分tektin-A,这表明低浓度的结构蛋白不存在膜相关或可溶性基质转运。然而,对生长中的纤毛的轴丝进行热分级分离后,结构残余物特有的标记蛋白在溶解的微管部分中占主导地位,这支持了生长过程中非微管蛋白与轴丝相关的运输,这与微管蛋白的膜/基质途径形成对比。

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