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酵母肌球蛋白II:非传统的传统肌球蛋白的一个新亚类?

Yeast myosin II: a new subclass of unconventional conventional myosins?

作者信息

May K M, Win T Z, Hyams J S

机构信息

Department of Biology, University College, London, UK.

出版信息

Cell Motil Cytoskeleton. 1998;39(3):195-200. doi: 10.1002/(SICI)1097-0169(1998)39:3<195::AID-CM2>3.0.CO;2-4.

Abstract

Myosin II is the founder member of a large and structurally diverse clan of actin-based motor proteins. The native myosin II molecule is a hexamer consisting of two heavy chains, two essential light chains (ELC), and two regulatory light chains (RLC). For convenience, the myosin IIs are often subdivided into four subclasses: vertebrate skeletal and cardiac muscle myosin II form one subclass, vertebrate smooth muscle and nonmuscle myosin II a second, invertebrate muscle a third, and protozoan myosin II a fourth [Sellers and Goodson, 1995]. Different mechanisms of regulation may exist between myosins within a single subclass yet all myosin IIs share a common three-domain structure; the N-terminus of the heavy chain forms two globular heads that contain the ATP- and actin-binding sites and the alpha-helical neck region that is stabilised by the binding of the two classes of light chains, whilst the C-terminus forms an extended coiled-coil tail that can consist of anywhere between 700 and 1,200 amino acids. In nonmuscle cells, myosin II has at least two well-defined functions, cell locomotion and cytokinesis. Yeast cells do not locomote, and their mechanism of cytokinesis involves the deposition of a cross-wall or septum. However, in the fission yeast, Schizosaccharomyces pombe, deposition of the septum is anticipated by the appearance of a contractile actomyosin ring [Marks and Hyams, 1985; May et al., 1997; Kitayama et al., 1997] and actin is also present at the bud neck during cytokinesis in the budding yeast, Saccharomyces cerevisiae [Kilmartin and Adams, 1984]. Here we report a phylogenetic analysis of the N-terminal head domains of the myosin IIs from both yeasts, a structural analysis of the tail domains of these proteins and we speculate as to the nature of the light chains that regulate their function. On the basis of these findings, we propose that the yeast myosin IIs constitute a divergent fifth class of "unconventional" conventional myosins.

摘要

肌球蛋白II是基于肌动蛋白的运动蛋白大家族中结构多样的创始成员。天然的肌球蛋白II分子是一个六聚体,由两条重链、两条必需轻链(ELC)和两条调节轻链(RLC)组成。为方便起见,肌球蛋白II通常分为四个亚类:脊椎动物骨骼肌和心肌肌球蛋白II为一个亚类,脊椎动物平滑肌和非肌肉肌球蛋白II为第二个亚类,无脊椎动物肌肉肌球蛋白II为第三个亚类,原生动物肌球蛋白II为第四个亚类[塞勒斯和古德森,1995年]。单个亚类中的肌球蛋白之间可能存在不同的调节机制,但所有肌球蛋白II都具有共同的三结构域结构;重链的N端形成两个球状头部,包含ATP和肌动蛋白结合位点,以及由两类轻链结合稳定的α螺旋颈部区域,而C端形成一个延伸的卷曲螺旋尾部,其长度可以在700到1200个氨基酸之间。在非肌肉细胞中,肌球蛋白II至少有两个明确的功能,即细胞运动和胞质分裂。酵母细胞不会移动,它们的胞质分裂机制涉及横壁或隔膜的沉积。然而,在裂殖酵母中,隔膜的沉积是由收缩性肌动球蛋白环的出现所预示的[马克斯和海姆斯,1985年;梅等人,1997年;北山等人,1997年],并且在芽殖酵母酿酒酵母的胞质分裂过程中,肌动蛋白也存在于芽颈处[基尔马丁和亚当斯,1984年]。在此,我们报告了对这两种酵母中肌球蛋白II的N端头部结构域的系统发育分析、这些蛋白质尾部结构域的结构分析,并推测了调节其功能的轻链的性质。基于这些发现,我们提出酵母肌球蛋白II构成了“非常规”传统肌球蛋白的一个不同的第五类。

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