Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R01 CA079057
NCI NIH HHS - United States
MOP97764
CIHR - Canada
MOP84412
CIHR - Canada
PubMed
24946904
PubMed Central
PMC4083431
DOI
10.1038/ncomms5181
PII: ncomms5181
Knihovny.cz E-zdroje
- MeSH
- adenosintrifosfatasy metabolismus MeSH
- analýza rozptylu MeSH
- bromodeoxyuridin MeSH
- chromatinová imunoprecipitace MeSH
- chromozomální proteiny, nehistonové metabolismus MeSH
- fluorescence MeSH
- galaktosidy MeSH
- histony metabolismus MeSH
- homeodoménové proteiny metabolismus MeSH
- hybridizace in situ MeSH
- imunohistochemie MeSH
- indoly MeSH
- koncové značení zlomů DNA in situ MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- metoda rotující tyčky MeSH
- mikročipová analýza MeSH
- morfogeneze genetika fyziologie MeSH
- mozeček embryologie MeSH
- myši transgenní MeSH
- myši MeSH
- nervové kmenové buňky metabolismus fyziologie MeSH
- počítačové zpracování obrazu MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- Purkyňovy buňky metabolismus MeSH
- restrukturace chromatinu fyziologie MeSH
- toloniumchlorid MeSH
- transmisní elektronová mikroskopie MeSH
- vývojová regulace genové exprese genetika fyziologie MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- 5-bromo-4-chloro-3-indolyl beta-galactoside MeSH Prohlížeč
- adenosintrifosfatasy MeSH
- bromodeoxyuridin MeSH
- chromozomální proteiny, nehistonové MeSH
- En1 protein, mouse MeSH Prohlížeč
- galaktosidy MeSH
- histony MeSH
- homeodoménové proteiny MeSH
- indoly MeSH
- Smarca5 protein, mouse MeSH Prohlížeč
- toloniumchlorid MeSH
Chromatin compaction mediates progenitor to post-mitotic cell transitions and modulates gene expression programs, yet the mechanisms are poorly defined. Snf2h and Snf2l are ATP-dependent chromatin remodelling proteins that assemble, reposition and space nucleosomes, and are robustly expressed in the brain. Here we show that mice conditionally inactivated for Snf2h in neural progenitors have reduced levels of histone H1 and H2A variants that compromise chromatin fluidity and transcriptional programs within the developing cerebellum. Disorganized chromatin limits Purkinje and granule neuron progenitor expansion, resulting in abnormal post-natal foliation, while deregulated transcriptional programs contribute to altered neural maturation, motor dysfunction and death. However, mice survive to young adulthood, in part from Snf2l compensation that restores Engrailed-1 expression. Similarly, Purkinje-specific Snf2h ablation affects chromatin ultrastructure and dendritic arborization, but alters cognitive skills rather than motor control. Our studies reveal that Snf2h controls chromatin organization and histone H1 dynamics for the establishment of gene expression programs underlying cerebellar morphogenesis and neural maturation.
Department of Cell Biology Albert Einstein College of Medicine Bronx New York 10461 USA
Regenerative Medicine Program Ottawa Hospital Research Institute Ottawa Ontario Canada K1H 8L6
Vision Program Ottawa Hospital Research Institute Ottawa Ontario Canada K1H 8L6
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GEO
GSE42371