SIRT6 deficiency results in developmental retardation in cynomolgus monkeys

Nature. 2018 Aug;560(7720):661-665. doi: 10.1038/s41586-018-0437-z. Epub 2018 Aug 22.

Abstract

SIRT6 acts as a longevity protein in rodents1,2. However, its biological function in primates remains largely unknown. Here we generate a SIRT6-null cynomolgus monkey (Macaca fascicularis) model using a CRISPR-Cas9-based approach. SIRT6-deficient monkeys die hours after birth and exhibit severe prenatal developmental retardation. SIRT6 loss delays neuronal differentiation by transcriptionally activating the long non-coding RNA H19 (a developmental repressor), and we were able to recapitulate this process in a human neural progenitor cell differentiation system. SIRT6 deficiency results in histone hyperacetylation at the imprinting control region of H19, CTCF recruitment and upregulation of H19. Our results suggest that SIRT6 is involved in regulating development in non-human primates, and may provide mechanistic insight into human perinatal lethality syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Animals, Newborn
  • Brain / cytology
  • Brain / embryology
  • CCCTC-Binding Factor / metabolism
  • Cell Differentiation / genetics
  • Developmental Disabilities / genetics*
  • Female
  • Fetal Death
  • Gene Deletion
  • Gene Editing
  • Genomic Imprinting
  • Histones / metabolism
  • Human Embryonic Stem Cells / cytology
  • Human Embryonic Stem Cells / metabolism
  • Humans
  • Macaca fascicularis / genetics*
  • Male
  • Muscles / cytology
  • Muscles / embryology
  • Neural Stem Cells / cytology
  • Neurogenesis / genetics
  • RNA, Long Noncoding / genetics
  • Sirtuins / deficiency*
  • Sirtuins / genetics*
  • Sirtuins / metabolism
  • Transcriptome / genetics

Substances

  • CCCTC-Binding Factor
  • H19 long non-coding RNA
  • Histones
  • RNA, Long Noncoding
  • Sirtuins