The stem cell-associated transcription co-factor, ZNF521, interacts with GLI1 and GLI2 and enhances the activity of the Sonic hedgehog pathway.
Animals
Cell Line
Cerebellar Neoplasms
/ genetics
Chromatin Assembly and Disassembly
/ genetics
Chromatin Immunoprecipitation
DNA-Binding Proteins
/ genetics
Databases, Genetic
Gene Expression Profiling
Gene Expression Regulation
/ genetics
Hedgehog Proteins
/ agonists
Histone Deacetylases
/ genetics
Humans
Medulloblastoma
/ genetics
Mice
Multigene Family
Nuclear Proteins
/ antagonists & inhibitors
Protein Binding
Signal Transduction
/ genetics
Up-Regulation
Zinc Finger Protein GLI1
/ antagonists & inhibitors
Zinc Finger Protein Gli2
/ antagonists & inhibitors
Journal
Cell death & disease
ISSN: 2041-4889
Titre abrégé: Cell Death Dis
Pays: England
ID NLM: 101524092
Informations de publication
Date de publication:
26 09 2019
26 09 2019
Historique:
received:
03
12
2018
accepted:
29
08
2019
revised:
17
08
2019
entrez:
28
9
2019
pubmed:
29
9
2019
medline:
28
8
2020
Statut:
epublish
Résumé
ZNF521 is a transcription co-factor with recognized regulatory functions in haematopoietic, osteo-adipogenic and neural progenitor cells. Among its diverse activities, ZNF521 has been implicated in the regulation of medulloblastoma (MB) cells, where the Hedgehog (HH) pathway, has a key role in the development of normal cerebellum and of a substantial fraction of MBs. Here a functional cross-talk is shown for ZNF521 with the HH pathway, where it interacts with GLI1 and GLI2, the major HH transcriptional effectors and enhances the activity of HH signalling. In particular, ZNF521 cooperates with GLI1 and GLI2 in the transcriptional activation of GLI (glioma-associated transcription factor)-responsive promoters. This synergism is dependent on the presence of the N-terminal, NuRD-binding motif in ZNF521, and is sensitive to HDAC (histone deacetylase) and GLI inhibitors. Taken together, these results highlight the role of ZNF521, and its interaction with the NuRD complex, in determining the HH response at the level of transcription. This may be of particular relevance in HH-driven diseases, especially regarding the MBs belonging to the SHH (sonic HH) subgroup where a high expression of ZNF521 is correlated with that of HH pathway components.
Identifiants
pubmed: 31558698
doi: 10.1038/s41419-019-1946-x
pii: 10.1038/s41419-019-1946-x
pmc: PMC6763495
doi:
Substances chimiques
DNA-Binding Proteins
0
GLI1 protein, human
0
GLI2 protein, human
0
Hedgehog Proteins
0
Nuclear Proteins
0
Zinc Finger Protein GLI1
0
Zinc Finger Protein Gli2
0
zinc finger protein 521, human
0
Histone Deacetylases
EC 3.5.1.98
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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