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基体定位和原生动物 RP2 和 FOR20 蛋白靶向的变化。

Variation in Basal Body Localisation and Targeting of Trypanosome RP2 and FOR20 Proteins.

机构信息

Faculty of Health and Medicine, Division of Biomedical and Life Sciences, Lancaster University, Lancaster LA1 4YQ, UK.

Department of Biological Sciences, School of Applied Sciences, University of Huddersfield, Queensgate, Huddersfield, HD1 3DH, UK.

出版信息

Protist. 2017 Aug;168(4):452-466. doi: 10.1016/j.protis.2017.07.002. Epub 2017 Jul 13.

Abstract

TOF-LisH-PLL motifs define FOP family proteins; some members are involved in flagellum assembly. The critical role of FOP family protein FOR20 is poorly understood. Here, we report relative localisations of the four FOP family proteins in parasitic Trypanosoma brucei: TbRP2, TbOFD1 and TbFOP/FOP1-like are mature basal body proteins whereas TbFOR20 is present on pro- and mature basal bodies - on the latter it localises distal to TbRP2. We discuss how the data, together with published work for another protist Giardia intestinalis, informs on likely FOR20 function. Moreover, our localisation study provides convincing evidence that the antigen recognised by monoclonal antibody YL1/2 at trypanosome mature basal bodies is FOP family protein TbRP2, not tyrosinated α-tubulin as widely stated in the literature. Curiously, FOR20 proteins from T. brucei and closely related African trypanosomes possess short, negatively-charged N-terminal extensions absent from FOR20 in other trypanosomatids and other eukaryotes. The extension is necessary for protein targeting, but insufficient to re-direct TbRP2 to probasal bodies. Yet, FOR20 from the American trypanosome T. cruzi, which lacks any extension, localises to pro- and mature basal bodies when expressed in T. brucei. This identifies unexpected variation in FOR20 architecture that is presently unique to one clade of trypanosomatids.

摘要

TOF-LisH-PLL 基序定义了 FOP 家族蛋白;有些成员参与鞭毛组装。FOP 家族蛋白 FOR20 的关键作用尚未被充分了解。在这里,我们报告了寄生的非洲锥虫 Trypanosoma brucei 中四个 FOP 家族蛋白的相对定位:TbRP2、TbOFD1 和 TbFOP/FOP1-like 是成熟基体蛋白,而 TbFOR20 存在于前基体和成熟基体上——在后基体上,它位于 TbRP2 的远端。我们讨论了这些数据,以及另一种原生动物贾第虫肠道的已发表工作,如何为 FOR20 功能提供信息。此外,我们的定位研究提供了令人信服的证据,证明被单克隆抗体 YL1/2 识别的抗原是成熟基体上的 FOP 家族蛋白 TbRP2,而不是文献中广泛报道的酪氨酸化α-微管蛋白。奇怪的是,来自非洲锥虫 T. brucei 和密切相关的锥虫的 FOR20 蛋白具有短的、带负电荷的 N 端延伸,而其他鞭毛原生动物和其他真核生物的 FOR20 中则没有。该延伸对于蛋白靶向是必需的,但不足以将 TbRP2 重新导向基体前体。然而,当在 T. brucei 中表达时,来自美洲锥虫 T. cruzi 的缺乏任何延伸的 FOR20 也能定位于前基体和成熟基体。这表明 FOR20 结构存在意外的变化,目前这种变化在一个锥虫类群中是独特的。

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