Fujii Junichi, Ochi Haruki, Yamada Sohsuke
Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Yamagata University, 2-2-2 Iidanishi, Yamagata, 990-9585, Japan.
Institute for Promotion of Medical Science Research, Faculty of Medicine, Yamagata University, 2-2-2 Iida-Nishi, Yamagata, 990-9585, Japan.
Free Radic Biol Med. 2025 Feb 1;227:336-354. doi: 10.1016/j.freeradbiomed.2024.12.015. Epub 2024 Dec 4.
Peroxiredoxin (PRDX) primarily employs electrons from thioredoxin in order to reduce peroxides. PRDX4 mainly resides either in the endoplasmic reticulum (ER) lumen or in extracellular spaces. Due to the usage of alternative promoters, a first exon is transcribed from different regions of the Prdx4 gene, which results in two types of mRNAs. The first type is designated as Prdx4. It is translated with a cleavable, hydrophobic signal sequence and is expressed in most cells throughout the body. The second type is designated as Prdx4t. The peroxidase activity of PRDX4 is involved in both the reduction of hydrogen peroxides and in the oxidative folding of nascent proteins in the ER. Prdx4 appears to have evolved from an ancestral gene in Eutherians simultaneously with the evolution of sperm protamine to cysteine-rich peptides, and, therefore, the testis-specific PRDX4t is likely involved in spermatogenesis through the oxidative folding of protamine. The dysfunction of PRDX4 leads to oxidative damage and ER stress, and is related to various diseases including diabetes and cancer. In this review article we refer to the results of biological and medical research in order to unveil the functional consequences of this unique member of the PRDX family.
过氧化物酶(PRDX)主要利用硫氧还蛋白的电子来还原过氧化物。PRDX4主要存在于内质网(ER)腔或细胞外空间。由于使用了不同的启动子,第一个外显子从Prdx4基因的不同区域转录,这导致了两种类型的mRNA。第一种类型被指定为Prdx4。它通过一个可切割的疏水信号序列进行翻译,并在全身大多数细胞中表达。第二种类型被指定为Prdx4t。PRDX4的过氧化物酶活性既参与过氧化氢的还原,也参与内质网中新生蛋白质的氧化折叠。Prdx4似乎与精子鱼精蛋白向富含半胱氨酸的肽的进化同时从真兽类的一个祖先基因进化而来,因此,睾丸特异性的PRDX4t可能通过鱼精蛋白的氧化折叠参与精子发生。PRDX4功能障碍会导致氧化损伤和内质网应激,并与包括糖尿病和癌症在内的各种疾病有关。在这篇综述文章中,我们参考生物学和医学研究结果,以揭示PRDX家族这一独特成员的功能后果。