Summary of ssbd-repos-000171

SSBD:database
URL

Name
ssbd-repos-000171 (171-Ochi-Hes1DynNPCs)
URL
DOI
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Title
Hes1 expression dynamics in the wild-type, Hes1 type-1 and Hes1 type-2 mutant NPCs of mice.
Description
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Submited Date
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Release Date
2021-09-30
Updated Date
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License
Funding information
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File formats
Data size
696.4 MB

Organism
Mus musculus
Strain
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Cell Line
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Genes
Hes1
Proteins
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GO Molecular Function (MF)
translation activator activity
GO Biological Process (BP)
gene expression
GO Cellular Component (CC)
NA
Study Type
Female, Homozygote, Theoretical, Transcription Factor HES-1/physiology, Gene Expression Regulation, Introns, Neurons/physiology, Mice, Cell Proliferation, Gene Expression Profiling, Models, Brain, Computer-Assisted, Transcription Factor HES-1, Developmental, Oscillometry, Neurons (D009474), Male, Image Processing, Cell Death, Animals, Cell Differentiation, Neural Stem Cells/cytology, Mutation, Brain/embryology, Neural Stem Cells, Neurogenesis
Imaging Methods
time lapse microscopy

Method Summary
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Related paper(s)

Shohei Ochi, Yui Imaizumi, Hiromi Shimojo, Hitoshi Miyachi, Ryoichiro Kageyama (2020) Oscillatory expression of Hes1 regulates cell proliferation and neuronal differentiation in the embryonic brain., Development (Cambridge, England), Volume 147, Number 4

Published in 2020 Feb 26 (Electronic publication in Feb. 26, 2020, midnight )

(Abstract) The expression of the transcriptional repressor Hes1 oscillates in many cell types, including neural progenitor cells (NPCs), but the significance of Hes1 oscillations in development is not fully understood. To examine the effect of altered oscillatory dynamics of Hes1, we generated two types of Hes1 knock-in mice, a shortened (type-1) and an elongated (type-2) Hes1 gene, and examined their phenotypes focusing on neural development. Although both mutations affected Hes1 oscillations, the type-1 mutation dampened Hes1 oscillations more severely, resulting in much lower amplitudes. The average levels of Hes1 expression in type-1 mutant NPCs were also lower than in wild-type NPCs but similar to or slightly higher than those in Hes1 heterozygous mutant mice, which exhibit no apparent defects. Whereas type-2 mutant mice were apparently normal, type-1 mutant mice displayed smaller brains than wild-type mice and upregulated proneural gene expression. Furthermore, proliferation of NPCs decreased and cell death increased in type-1 mutant embryos. When Hes3 and Hes5 were additionally deleted, neuronal differentiation was also accelerated, leading to microcephaly. Thus, robust Hes1 oscillations are required for maintenance and proliferation of NPCs and the normal timing of neurogenesis, thereby regulating brain morphogenesis.
(MeSH Terms)

Contact(s)
Ryoichiro Kageyama
Organization(s)
Kyoto University , Institute for Frontier Life and Medical Sciences
Image Data Contributors
Quantitative Data Contributors

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