线粒体δ -1-吡咯-5-羧酸脱氢酶(ALDH4A1)的序列、系统发育和进化。果蝇中第二个基因座(ALDH4A2)的证据。

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Roger S. Holmes
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引用次数: 0

摘要

ALDH4A1基因编码δ-1-吡咯啉-5-羧酸盐代谢的线粒体酶,从脯氨酸或鸟氨酸产生谷氨酸。使用已报道的人类和小鼠ALDH4A1氨基酸序列对几种脊椎动物和无脊椎动物基因组进行了分析。ALDH4A1序列和结构是高度保守的,包括参与催化、辅酶结合和酶结构的残基,先前报道了小鼠和人ALDH4A1。人类ALDH4A1基因包含15个编码外显子,在人类肝脏和肾脏皮层中表达更高。脊椎动物ALDH4A1线粒体前导序列表现出不同的序列。系统发育研究支持ALDH4A1基因在无脊椎动物进化中的出现,该基因在随后的脊椎动物进化过程中一直作为单一的ALDH4A1基因被保守和保留。例外情况包括大西洋三文鱼(Salmo salar)和非洲蟾蜍(Xenopus laevis)基因的多倍体。对相关果蝇物种的ALDH4A1序列的检查支持了第二个ALDH4A基因(ALDH4A2)的出现以及这两个基因在过去5000万年中的时间依赖性进化变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sequences, phylogeny and evolution of mitochondrial delta-1-pyrroline-5-carboxylate dehydrogenases (ALDH4A1). Evidence for a second locus (ALDH4A2) in Drosophila

ALDH4A1 genes encode mitochondrial enzymes of delta-1-pyrroline-5-carboxylate metabolism, generating glutamate from either proline or ornithine. Analyses were undertaken of several vertebrate and invertebrate genomes using reported human and mouse ALDH4A1 amino acid sequences. ALDH4A1 sequences and structures were highly conserved, including residues involved in catalysis, coenzyme binding and enzyme structure, previously reported for mouse and human ALDH4A1. The human ALDH4A1 gene contained 15 coding exons and was more highly expressed in human liver and kidney cortex. Vertebrate ALDH4A1 mitochondrial leader sequences exhibited diverse sequences. Phylogeny studies supported the appearance of the ALDH4A1 gene in invertebrate evolution which has been conserved and retained throughout subsequent vertebrate evolution as a single ALDH4A1 gene. Exceptions included polyploidy observed for the Atlantic salmon (Salmo salar) and African toad (Xenopus laevis) genes. An examination of ALDH4A1 sequences from related Drosophila species supported the appearance of a second ALDH4A gene (ALDH4A2) and time dependent evolutionary changes over the past 50 million years for both genes.

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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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