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Datamining approaches for examining the low prevalence of N-acetylglutamate synthase deficiency and understanding transcriptional regulation of urea cycle genes.
Caldovic, Ljubica; Ahn, Julie J; Andricovic, Jacklyn; Balick, Veronica M; Brayer, Mallory; Chansky, Pamela A; Dawson, Tyson; Edwards, Alex C; Felsen, Sara E; Ismat, Karim; Jagannathan, Sveta V; Mann, Brendan T; Medina, Jacob A; Morizono, Toshio; Morizono, Michio; Salameh, Shatha; Vashist, Neerja; Williams, Emily C; Zhou, Zhe; Morizono, Hiroki.
Affiliation
  • Caldovic L; Center for Genetic Medicine Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.
  • Ahn JJ; Department of Genomics and Precision Medicine, School of Medicine and Health Sciences, The George Washington University, Washington, DC, USA.
  • Andricovic J; Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
  • Balick VM; Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
  • Brayer M; Department of Biochemistry and Molecular Medicine, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
  • Chansky PA; Department of Biological Sciences, The George Washington University, Washington, DC, USA.
  • Dawson T; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Edwards AC; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Felsen SE; AMPEL BioSolutions LLC, Charlottesville, Virginia, USA.
  • Ismat K; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Jagannathan SV; Center for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.
  • Mann BT; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Medina JA; Center for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.
  • Morizono T; Center for Genetic Medicine Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.
  • Morizono M; Department of Genomics and Precision Medicine, School of Medicine and Health Sciences, The George Washington University, Washington, DC, USA.
  • Salameh S; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Vashist N; Department of Microbiology, Immunology, and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Williams EC; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
  • Zhou Z; College of Science and Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
  • Morizono H; College of Science and Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
J Inherit Metab Dis ; 2023 Oct 17.
Article in En | MEDLINE | ID: mdl-37847851
Ammonia, which is toxic to the brain, is converted into non-toxic urea, through a pathway of six enzymatically catalyzed steps known as the urea cycle. In this pathway, N-acetylglutamate synthase (NAGS, EC 2.3.1.1) catalyzes the formation of N-acetylglutamate (NAG) from glutamate and acetyl coenzyme A. NAGS deficiency (NAGSD) is the rarest of the urea cycle disorders, yet is unique in that ureagenesis can be restored with the drug N-carbamylglutamate (NCG). We investigated whether the rarity of NAGSD could be due to low sequence variation in the NAGS genomic region, high NAGS tolerance for amino acid replacements, and alternative sources of NAG and NCG in the body. We also evaluated whether the small genomic footprint of the NAGS catalytic domain might play a role. The small number of patients diagnosed with NAGSD could result from the absence of specific disease biomarkers and/or short NAGS catalytic domain. We screened for sequence variants in NAGS regulatory regions in patients suspected of having NAGSD and found a novel NAGS regulatory element in the first intron of the NAGS gene. We applied the same datamining approach to identify regulatory elements in the remaining urea cycle genes. In addition to the known promoters and enhancers of each gene, we identified several novel regulatory elements in their upstream regions and first introns. The identification of cis-regulatory elements of urea cycle genes and their associated transcription factors holds promise for uncovering shared mechanisms governing urea cycle gene expression and potentially leading to new treatments for urea cycle disorders.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Inherit Metab Dis Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Inherit Metab Dis Year: 2023 Type: Article Affiliation country: United States