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The status of the human gene catalogue.
Amaral, Paulo; Carbonell-Sala, Silvia; De La Vega, Francisco M; Faial, Tiago; Frankish, Adam; Gingeras, Thomas; Guigo, Roderic; Harrow, Jennifer L; Hatzigeorgiou, Artemis G; Johnson, Rory; Murphy, Terence D; Pertea, Mihaela; Pruitt, Kim D; Pujar, Shashikant; Takahashi, Hazuki; Ulitsky, Igor; Varabyou, Ales; Wells, Christine A; Yandell, Mark; Carninci, Piero; Salzberg, Steven L.
Afiliação
  • Amaral P; INSPER Institute of Education and Research, Sao Paulo, Brazil.
  • Carbonell-Sala S; Centre for Genomic Regulation (CRG), Barcelona, Spain.
  • De La Vega FM; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.
  • Faial T; Tempus Labs, Chicago, IL, USA.
  • Frankish A; Nature Genetics, San Francisco, CA, USA.
  • Gingeras T; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, UK.
  • Guigo R; Department of Functional Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.
  • Harrow JL; Centre for Genomic Regulation (CRG), Barcelona, Spain.
  • Hatzigeorgiou AG; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Johnson R; Centre for Genomics Research, Discovery Sciences, AstraZeneca, Royston, UK.
  • Murphy TD; Department of Computer Science and Biomedical Informatics, Universithy of Thessaly, Lamia, Greece.
  • Pertea M; Hellenic Pasteur Institute, Athens, Greece.
  • Pruitt KD; School of Biology and Environmental Science, University College Dublin, Dublin, Ireland.
  • Pujar S; Conway Institute of Biomedical and Biomolecular Research, University College Dublin, Dublin, Ireland.
  • Takahashi H; Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Ulitsky I; Department for BioMedical Research, University of Bern, Bern, Switzerland.
  • Varabyou A; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.
  • Wells CA; Center for Computational Biology, Johns Hopkins University, Baltimore, MD, USA.
  • Yandell M; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA.
  • Carninci P; Department of Computer Science, Johns Hopkins University, Baltimore, MD, USA.
  • Salzberg SL; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.
Nature ; 622(7981): 41-47, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37794265
ABSTRACT
Scientists have been trying to identify every gene in the human genome since the initial draft was published in 2001. In the years since, much progress has been made in identifying protein-coding genes, currently estimated to number fewer than 20,000, with an ever-expanding number of distinct protein-coding isoforms. Here we review the status of the human gene catalogue and the efforts to complete it in recent years. Beside the ongoing annotation of protein-coding genes, their isoforms and pseudogenes, the invention of high-throughput RNA sequencing and other technological breakthroughs have led to a rapid growth in the number of reported non-coding RNA genes. For most of these non-coding RNAs, the functional relevance is currently unclear; we look at recent advances that offer paths forward to identifying their functions and towards eventually completing the human gene catalogue. Finally, we examine the need for a universal annotation standard that includes all medically significant genes and maintains their relationships with different reference genomes for the use of the human gene catalogue in clinical settings.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Isoformas de Proteínas / Anotação de Sequência Molecular / Genes Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nature Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Isoformas de Proteínas / Anotação de Sequência Molecular / Genes Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nature Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Brasil