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序列分析揭示了鞭毛辐条的两种蛋白质之间的同源性。

Sequence analysis reveals homology between two proteins of the flagellar radial spoke.

作者信息

Curry A M, Williams B D, Rosenbaum J L

机构信息

Department of Biology, Yale University, New Haven, Connecticut 06511.

出版信息

Mol Cell Biol. 1992 Sep;12(9):3967-77. doi: 10.1128/mcb.12.9.3967-3977.1992.

Abstract

Flagellar radial spokes contribute to the regulation of dynein arm activity and thus the pattern of flagellar bending. We have sequenced the genes for radial spoke protein 4 (RSP4) and RSP6, two of the five proteins that make up the radial spoke head in Chlamydomonas reinhardtii. The two genes, which are tightly linked genetically (B. Huang, G. Piperno, Z. Ramanis, and D.J.L. Luck, J. Cell Biol. 88:80-88, 1981), are separated by only 435 bp. They encode proline-rich polypeptides of 49.8 kDa (RSP4) and 48.8 kDa (RSP6), which are 48% identical to each other but do not resemble any previously sequenced proteins. The transcription start sites of these genes and an additional radial spoke protein gene, that for RSP3, were determined, and patterns of mRNA accumulation during flagellar regeneration were examined for the three radial spoke protein genes. These studies provide the molecular tools for a detailed analysis of radial spoke head function and assembly and for a determination of the mechanism by which the genes required to build a complex organelle are regulated.

摘要

鞭毛辐条有助于调节动力蛋白臂的活性,从而影响鞭毛弯曲的模式。我们已经对莱茵衣藻中构成辐条头部的五种蛋白质中的两种——辐条蛋白4(RSP4)和RSP6的基因进行了测序。这两个基因在遗传上紧密连锁(B. Huang、G. Piperno、Z. Ramanis和D.J.L. Luck,《细胞生物学杂志》88:80 - 88,1981),仅相隔435个碱基对。它们编码富含脯氨酸的多肽,分别为49.8 kDa(RSP4)和48.8 kDa(RSP6),二者彼此有48%的同源性,但与之前测序的任何蛋白质都不相似。确定了这些基因以及另一个辐条蛋白基因(RSP3基因)的转录起始位点,并检测了这三个辐条蛋白基因在鞭毛再生过程中的mRNA积累模式。这些研究为详细分析辐条头部的功能和组装以及确定构建复杂细胞器所需基因的调控机制提供了分子工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5156/360281/a1630a243a2f/molcellb00132-0315-a.jpg

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