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Epigenetic control of chromosome-associated lncRNA genes essential for replication and stability.
Heskett, Michael B; Vouzas, Athanasios E; Smith, Leslie G; Yates, Phillip A; Boniface, Christopher; Bouhassira, Eric E; Spellman, Paul T; Gilbert, David M; Thayer, Mathew J.
Affiliation
  • Heskett MB; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.
  • Vouzas AE; Department of Molecular and Medical Genetics Oregon Health & Science University, Portland, OR, 97239, USA.
  • Smith LG; Department of Biological Science, Florida State University, Tallahassee, FL, 32306, USA.
  • Yates PA; Department of Chemical Physiology and Biochemistry Oregon Health & Science University, Portland, OR, 97239, USA.
  • Boniface C; Department of Chemical Physiology and Biochemistry Oregon Health & Science University, Portland, OR, 97239, USA.
  • Bouhassira EE; Cancer Early Detection Advanced Research Center, Knight Cancer Institute Oregon Health & Science University, Portland, OR, 97239, USA.
  • Spellman PT; Department of Cell Biology and Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
  • Gilbert DM; Department of Molecular and Medical Genetics Oregon Health & Science University, Portland, OR, 97239, USA.
  • Thayer MJ; Cancer Early Detection Advanced Research Center, Knight Cancer Institute Oregon Health & Science University, Portland, OR, 97239, USA.
Nat Commun ; 13(1): 6301, 2022 10 22.
Article in En | MEDLINE | ID: mdl-36273230
ABSTRACT
ASARs are long noncoding RNA genes that control replication timing of entire human chromosomes in cis. The three known ASAR genes are located on human chromosomes 6 and 15, and are essential for chromosome integrity. To identify ASARs on all human chromosomes we utilize a set of distinctive ASAR characteristics that allow for the identification of hundreds of autosomal loci with epigenetically controlled, allele-restricted behavior in expression and replication timing of coding and noncoding genes, and is distinct from genomic imprinting. Disruption of noncoding RNA genes at five of five tested loci result in chromosome-wide delayed replication and chromosomal instability, validating their ASAR activity. In addition to the three known essential cis-acting chromosomal loci, origins, centromeres, and telomeres, we propose that all mammalian chromosomes also contain "Inactivation/Stability Centers" that display allele-restricted epigenetic regulation of protein coding and noncoding ASAR genes that are essential for replication and stability of each chromosome.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Long Noncoding Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2022 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Long Noncoding Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2022 Document type: Article Affiliation country: United States