The many roles of the Alzheimer-associated gene PM20D1

Diana Garro-Núñez, Pablo Mora-Cubillo, Sammy Fonseca-Bone, María Jesús Picado-Martínez, Michael Fonseca-Brenes, Henriette Raventós-Vorst, Gabriela Chavarría-Soley
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Abstract

PM20D1 is a little studied enzyme until recently, belonging to the mammalian M20 peptidase family, which catalyzes both the synthesis and hydrolysis of N-acyl amino acids (NAAs). NAAs are bioactive lipids biosynthesized from free fatty acids and free amino acids. These molecules have been associated with many biological functions; however, most of the biochemical mechanisms have not yet been described. The best-known biochemical mechanism is the one involved in thermogenesis, which also has implications for reactive oxygen species levels and cell preservation. In the last few years, genetic variation in PM20D1, as well as changes in its methylation and expression levels, have been reported to be associated with several disease phenotypes, including Alzheimer’s disease. In this review, we explore the current knowledge regarding the PM20D1 gene, including aspects such as its biology, potential functions, regulation of its expression, and role in different phenotypes such as Alzheimer’s disease, obesity, Parkinson’s disease, and several other disorders.
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阿尔茨海默病相关基因PM20D1的许多作用
PM20D1是一种研究较少的酶,属于哺乳动物M20肽酶家族,催化n -酰基氨基酸(NAAs)的合成和水解。NAAs是由游离脂肪酸和游离氨基酸生物合成的具有生物活性的脂质。这些分子与许多生物功能有关;然而,大多数生物化学机制尚未被描述。最著名的生化机制是产热机制,它也涉及活性氧水平和细胞保存。在过去几年中,PM20D1的遗传变异及其甲基化和表达水平的变化被报道与几种疾病表型相关,包括阿尔茨海默病。在这篇综述中,我们探讨了PM20D1基因的现有知识,包括其生物学、潜在功能、表达调控以及在不同表型(如阿尔茨海默病、肥胖、帕金森病和其他几种疾病)中的作用。
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