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钙池结合蛋白结构的系统发生和生化分析及其变体与心脏疾病的关联。

Phylogenetic and biochemical analysis of calsequestrin structure and association of its variants with cardiac disorders.

机构信息

Department of Biochemistry, University of Alberta, Edmonton, Alberta, T6G 2H7, Canada.

Division of Infectious Disease, Department of Medicine, University of Alberta, Edmonton, AB, T6G 2G3, Canada.

出版信息

Sci Rep. 2020 Oct 22;10(1):18115. doi: 10.1038/s41598-020-75097-3.

Abstract

Calsequestrin is among the most abundant proteins in muscle sarcoplasmic reticulum and displays a high capacity but a low affinity for Ca binding. In mammals, calsequestrin is encoded by two genes, CASQ1 and CASQ2, which are expressed almost exclusively in skeletal and cardiac muscles, respectively. Phylogenetic analysis indicates that calsequestrin is an ancient gene in metazoans, and that the duplication of the ancestral calsequestrin gene took place after the emergence of the lancelet. CASQ2 gene variants associated with catecholaminergic polymorphic ventricular tachycardia (CPVT) in humans are positively correlated with a high degree of evolutionary conservation across all calsequestrin homologues. The mutations are distributed in diverse locations of the calsequestrin protein and impart functional diversity but remarkably manifest in a similar phenotype in humans.

摘要

钙结合蛋白封端蛋白是肌肉肌浆网中最丰富的蛋白质之一,具有高容量但低亲和力的钙结合能力。在哺乳动物中,钙结合蛋白封端蛋白由两个基因 CASQ1 和 CASQ2 编码,它们分别在骨骼肌和心肌中几乎特异性表达。系统发生分析表明钙结合蛋白封端蛋白是后生动物中的一个古老基因,在被囊动物出现后,祖先钙结合蛋白封端蛋白基因发生了复制。与人类儿茶酚胺多形性室性心动过速(CPVT)相关的 CASQ2 基因突变与所有钙结合蛋白同源物的高度进化保守性呈正相关。这些突变分布在钙结合蛋白封端蛋白的不同位置,赋予了功能多样性,但在人类中却表现出惊人的相似表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab0f/7582152/cf447d332c9c/41598_2020_75097_Fig1_HTML.jpg

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