Anthony Antonellis, Maximiliano Barrientos, Eva Bensasson, Teri DeClercq, Pablo Garrigós, Rachel Heilmann, Rita Horvath, Desiree Magee, Angelica Moresco, Ashley Rowland, Ingrid Vallee, Rebecca Alexander, Haissi Cui, Ita Gruić-Sovulj, Tamara L. Hendrickson, Sunghoon Kim, Jiqiang Ling, Susan A. Martinis, Karin Musier-Forsyth, Xiang-Lei Yang, Ilka U. Heinemann, Lluis Ribas de Pouplana
{"title":"A call for unified use of human aminoacyl-tRNA synthetase (ARS) gene nomenclature","authors":"Anthony Antonellis, Maximiliano Barrientos, Eva Bensasson, Teri DeClercq, Pablo Garrigós, Rachel Heilmann, Rita Horvath, Desiree Magee, Angelica Moresco, Ashley Rowland, Ingrid Vallee, Rebecca Alexander, Haissi Cui, Ita Gruić-Sovulj, Tamara L. Hendrickson, Sunghoon Kim, Jiqiang Ling, Susan A. Martinis, Karin Musier-Forsyth, Xiang-Lei Yang, Ilka U. Heinemann, Lluis Ribas de Pouplana","doi":"10.1002/1873-3468.70418","DOIUrl":null,"url":null,"abstract":"<p>Aminoacyl-tRNA synthetases (ARSs) are a family of enzymes that attach amino acids to tRNAs. To date, all 37 human ARS genes have been implicated in genetic diseases, affecting over a thousand patients worldwide. At the 2025 Federation of European Biochemical Societies (FEBS) Special Meeting ‘Expanding Frontiers in Aminoacyl-tRNA Synthetase Research’, patients, families, and advocacy groups communicated the need for a unified approach for reporting on ARS gene names and associated conditions in the scientific literature. This request stemmed from the current use of multiple nomenclature systems and the desire of these individuals to rapidly identify published data on specific ARS genes. Here, we summarize ARS gene nomenclature and request that the scientific community adhere to a single nomenclature system.</p>","PeriodicalId":12142,"journal":{"name":"FEBS Letters","volume":"600 16","pages":"2211-2218"},"PeriodicalIF":3.0000,"publicationDate":"2026-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/1873-3468.70418","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEBS Letters","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/1873-3468.70418","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Aminoacyl-tRNA synthetases (ARSs) are a family of enzymes that attach amino acids to tRNAs. To date, all 37 human ARS genes have been implicated in genetic diseases, affecting over a thousand patients worldwide. At the 2025 Federation of European Biochemical Societies (FEBS) Special Meeting ‘Expanding Frontiers in Aminoacyl-tRNA Synthetase Research’, patients, families, and advocacy groups communicated the need for a unified approach for reporting on ARS gene names and associated conditions in the scientific literature. This request stemmed from the current use of multiple nomenclature systems and the desire of these individuals to rapidly identify published data on specific ARS genes. Here, we summarize ARS gene nomenclature and request that the scientific community adhere to a single nomenclature system.
期刊介绍:
FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.