Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cells

Satoshi Kawase, Takao Imai, Chikako Miyauchi-Hara, Kunio Yaguchi, Yoshinori Nishimoto, Shin Ichi Fukami, Yumi Matsuzaki, Atsushi Miyawaki, Shigeyoshi Itohara, Hideyuki Okano

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Abstract

Background: The specific genetic regulation of neural primordial cell determination is of great interest in stem cell biology. The Musashi1 (Msi1) protein, which belongs to an evolutionarily conserved family of RNA-binding proteins, is a marker for neural stem/progenitor cells (NS/PCs) in the embryonic and post-natal central nervous system (CNS). Msi1 regulates the translation of its downstream targets, including m-Numb and p21 mRNAs. In vitro experiments using knockout mice have shown that Msi1 and its isoform Musashi2 (Msi2) keep NS/PCs in an undifferentiated and proliferative state. Msi1 is expressed not only in NS/PCs, but also in other somatic stem cells and in tumours. Based on previous findings, Msi1 is likely to be a key regulator for maintaining the characteristics of self-renewing stem cells. However, the mechanisms regulating Msi1 expression are not yet clear. Results: To identify the DNA region affecting Msi1 transcription, we inserted the fusion gene ffLuc, comprised of the fluorescent Venus protein and firefly Luciferase, at the translation initiation site of the mouse Msi1 gene locus contained in a 184-kb bacterial artificial chromosome (BAC). Fluorescence and Luciferase activity, reflecting the Msi1 transcriptional activity, were observed in a stable BAC-carrying embryonic stem cell line when it was induced toward neural lineage differentiation by retinoic acid treatment. When neuronal differentiation was induced in embryoid body (EB)-derived neurosphere cells, reporter signals were detected in Msi1-positive NSCs and GFAP-positive astrocytes, but not in MAP2-positive neurons. By introducing deletions into the BAC reporter gene and conducting further reporter experiments using a minimized enhancer region, we identified a region, "D5E2," that is responsible for Msi1 transcription in NS/PCs. Conclusions: A regulatory element for Msi1 transcription in NS/PCs is located in the sixth intron of the Msi1 gene. The 595-bp D5E2 intronic enhancer can transactivate Msi1 gene expression with cell-type specificity markedly similar to the endogenous Msi1 expression patterns.

Original languageEnglish
Article number14
JournalMolecular Brain
Volume4
Issue number1
DOIs
Publication statusPublished - 2011

Fingerprint

Neural Stem Cells
Stem Cells
Bacterial Artificial Chromosomes
Venus
Embryoid Bodies
Firefly Luciferases
Adult Stem Cells
RNA-Binding Proteins
Gene Fusion
Embryonic Stem Cells
Tretinoin
Luciferases
Reporter Genes
Knockout Mice
Astrocytes
Introns
Genes
Cell Biology
Protein Isoforms
Proteins

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Molecular Biology

Cite this

Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cells. / Kawase, Satoshi; Imai, Takao; Miyauchi-Hara, Chikako; Yaguchi, Kunio; Nishimoto, Yoshinori; Fukami, Shin Ichi; Matsuzaki, Yumi; Miyawaki, Atsushi; Itohara, Shigeyoshi; Okano, Hideyuki.

In: Molecular Brain, Vol. 4, No. 1, 14, 2011.

Research output: Contribution to journalArticle

Kawase, S, Imai, T, Miyauchi-Hara, C, Yaguchi, K, Nishimoto, Y, Fukami, SI, Matsuzaki, Y, Miyawaki, A, Itohara, S & Okano, H 2011, 'Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cells', Molecular Brain, vol. 4, no. 1, 14. https://doi.org/10.1186/1756-6606-4-14
Kawase, Satoshi ; Imai, Takao ; Miyauchi-Hara, Chikako ; Yaguchi, Kunio ; Nishimoto, Yoshinori ; Fukami, Shin Ichi ; Matsuzaki, Yumi ; Miyawaki, Atsushi ; Itohara, Shigeyoshi ; Okano, Hideyuki. / Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cells. In: Molecular Brain. 2011 ; Vol. 4, No. 1.
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