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铁还原酶结构域(FRD)超家族的进化:模块性、功能多样化和特征基序。

Evolution of the ferric reductase domain (FRD) superfamily: modularity, functional diversification, and signature motifs.

机构信息

Department of Biochemistry, Science II, University of Geneva, Geneva, Switzerland.

出版信息

PLoS One. 2013;8(3):e58126. doi: 10.1371/journal.pone.0058126. Epub 2013 Mar 7.

Abstract

A heme-containing transmembrane ferric reductase domain (FRD) is found in bacterial and eukaryotic protein families, including ferric reductases (FRE), and NADPH oxidases (NOX). The aim of this study was to understand the phylogeny of the FRD superfamily. Bacteria contain FRD proteins consisting only of the ferric reductase domain, such as YedZ and short bFRE proteins. Full length FRE and NOX enzymes are mostly found in eukaryotic cells and all possess a dehydrogenase domain, allowing them to catalyze electron transfer from cytosolic NADPH to extracellular metal ions (FRE) or oxygen (NOX). Metazoa possess YedZ-related STEAP proteins, possibly derived from bacteria through horizontal gene transfer. Phylogenetic analyses suggests that FRE enzymes appeared early in evolution, followed by a transition towards EF-hand containing NOX enzymes (NOX5- and DUOX-like). An ancestral gene of the NOX(1-4) family probably lost the EF-hands and new regulatory mechanisms of increasing complexity evolved in this clade. Two signature motifs were identified: NOX enzymes are distinguished from FRE enzymes through a four amino acid motif spanning from transmembrane domain 3 (TM3) to TM4, and YedZ/STEAP proteins are identified by the replacement of the first canonical heme-spanning histidine by a highly conserved arginine. The FRD superfamily most likely originated in bacteria.

摘要

一个含血红素的跨膜铁还原酶结构域(FRD)存在于细菌和真核蛋白家族中,包括铁还原酶(FRE)和 NADPH 氧化酶(NOX)。本研究旨在了解 FRD 超家族的系统发育。细菌中含有仅由铁还原酶结构域组成的 FRD 蛋白,如 YedZ 和短 bFRE 蛋白。全长 FRE 和 NOX 酶主要存在于真核细胞中,均具有脱氢酶结构域,使其能够催化细胞质 NADPH 向细胞外金属离子(FRE)或氧气(NOX)的电子转移。原生动物具有与 YedZ 相关的 STEAP 蛋白,可能通过水平基因转移来自细菌。系统发育分析表明,FRE 酶在进化早期出现,随后过渡到含有 EF 手的 NOX 酶(NOX5-和 DUOX 样)。NOX(1-4)家族的祖先基因可能失去了 EF 手,并且在这个分支中进化出了越来越复杂的新调节机制。确定了两个特征基序:通过跨越从跨膜域 3(TM3)到 TM4 的四个氨基酸基序将 NOX 酶与 FRE 酶区分开来,并且通过用高度保守的精氨酸取代第一个典型的血红素跨越组氨酸来鉴定 YedZ/STEAP 蛋白。FRD 超家族很可能起源于细菌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f2b/3591440/75f8198c3979/pone.0058126.g001.jpg

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