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特定氨基酸在β-微管蛋白亚型对神经元生长和维持中的可能作用:来自头足类软体动物的新见解

Possible Roles of Specific Amino Acids in β-Tubulin Isotypes in the Growth and Maintenance of Neurons: Novel Insights From Cephalopod Mollusks.

作者信息

Ludueña Richard F

机构信息

Department of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.

出版信息

Front Mol Neurosci. 2022 Apr 14;15:838393. doi: 10.3389/fnmol.2022.838393. eCollection 2022.

Abstract

Microtubules, are formed of the protein tubulin, which is a heterodimer of α- and β-tubulin subunits. Both α- and β-tubulin exist as numerous isotypes, differing in amino acid sequence and tissue distribution. Among the vertebrate β isotypes, βIII has a very narrow distribution, being found primarily in neurons and in advanced cancers. The places in the amino acid sequence where βIII differs from the other β isotypes are highly conserved in evolution. βIII appears to be highly resistant to reactive oxygen species and it forms highly dynamic microtubules. The first property would be very useful in neurons, which have high concentrations of free radicals, and the high dynamicity would aid neurite outgrowth. The same properties make βIII useful in cancers. Examination of the amino acid sequences indicates a cysteine cluster at positions 124-129 in βIII (CXXCXC). This occurs in all βIII isotypes but not in βI, βII, or βIV. βIII also lacks the easily oxidized C239. Both features could play roles in free radical resistance. Many aggressive tumors over-express βIII. However, a recent study of breast cancer patients showed that many of them mutated their βI, βII, and βIV at particular places to change the residues to those found at the corresponding sites in βIII; these are all sites that are highly conserved in vertebrate βIII. It is possible that these residues are important, not only in the resistance to free radicals, but also in the high dynamicity of βIII. The cephalopod mollusks are well known to be highly intelligent and can remodel their own brains. Interestingly, several cephalopods contain the cysteine cluster as well as up to 7 of the 17 residues that are highly conserved in vertebrate βIII, but are not found in βI, βII, or βIV. In short, it is possible that we are looking at a case of convergent evolution, that a βIII-like isotype may be required for neuronal growth and function and that a structure-function study of the particular residues conserved between vertebrate βIII and cephalopod tubulin isotypes could greatly increase our understanding of the role of the various tubulin isotypes in neuronal growth and function and could aid in the development of novel anti-tumor drugs.

摘要

微管由微管蛋白构成,微管蛋白是α - 微管蛋白亚基和β - 微管蛋白亚基组成的异二聚体。α - 微管蛋白和β - 微管蛋白都有多种同种型,其氨基酸序列和组织分布各不相同。在脊椎动物的β同种型中,βIII的分布非常狭窄,主要存在于神经元和晚期癌症中。βIII与其他β同种型在氨基酸序列上不同的位置在进化过程中高度保守。βIII似乎对活性氧具有高度抗性,并且它形成高度动态的微管。第一个特性在自由基浓度高的神经元中非常有用,而高动态性有助于神经突生长。同样的特性使βIII在癌症中也很有用。对氨基酸序列的研究表明,βIII中124 - 129位存在一个半胱氨酸簇(CXXCXC)。所有βIII同种型都有此结构,但βI、βII或βIV中没有。βIII也缺乏易被氧化的C239。这两个特征都可能在抗自由基中发挥作用。许多侵袭性肿瘤过度表达βIII。然而,最近一项针对乳腺癌患者的研究表明,他们中的许多人在特定位置使βI、βII和βIV发生突变,将这些残基变为βIII相应位点上发现的残基;这些都是脊椎动物βIII中高度保守的位点。这些残基不仅可能在抗自由基方面很重要,而且在βIII的高动态性方面也很重要似乎是有可能的。头足类软体动物以其高度智能且能重塑自身大脑而闻名。有趣的是,几种头足类动物含有半胱氨酸簇以及脊椎动物βIII中17个高度保守残基中的多达7个,而这些残基在βI、βII或βIV中不存在。简而言之,有可能我们正在研究一个趋同进化的例子,即神经元生长和功能可能需要一种类似βIII的同种型,并且对脊椎动物βIII和头足类微管蛋白同种型之间保守的特定残基进行结构 - 功能研究可能会极大地增进我们对各种微管蛋白同种型在神经元生长和功能中作用的理解,并有助于开发新型抗肿瘤药物。

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