Stabilizing heterochromatin by DGCR8 alleviates senescence and osteoarthritis.
Animals
Cellular Senescence
Heterochromatin
/ genetics
Humans
Lamin Type B
/ genetics
Male
Mesenchymal Stem Cells
/ metabolism
Mice
Mice, Inbred C57BL
Mice, Inbred NOD
MicroRNAs
/ genetics
Osteoarthritis
/ genetics
Protein Stability
RNA-Binding Proteins
/ genetics
Tripartite Motif-Containing Protein 28
/ genetics
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
26 07 2019
26 07 2019
Historique:
received:
17
05
2018
accepted:
03
06
2019
entrez:
28
7
2019
pubmed:
28
7
2019
medline:
31
12
2019
Statut:
epublish
Résumé
DiGeorge syndrome critical region 8 (DGCR8) is a critical component of the canonical microprocessor complex for microRNA biogenesis. However, the non-canonical functions of DGCR8 have not been studied. Here, we demonstrate that DGCR8 plays an important role in maintaining heterochromatin organization and attenuating aging. An N-terminal-truncated version of DGCR8 (DR8
Identifiants
pubmed: 31350386
doi: 10.1038/s41467-019-10831-8
pii: 10.1038/s41467-019-10831-8
pmc: PMC6659673
doi:
Substances chimiques
DGCR8 protein, human
0
Dgcr8 protein, mouse
0
Heterochromatin
0
Lamin Type B
0
MicroRNAs
0
RNA-Binding Proteins
0
TRIM28 protein, human
EC 2.3.2.27
Tripartite Motif-Containing Protein 28
EC 2.3.2.27
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3329Références
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