Mesodermal- Vs. neuronal-specific expression of MafK is elicited by different promoters

Hozumi Motohashi, Kazuhiko Igarashi, Kou Onodera, Satoru Takahashi, Haruo Ohtani, Masato Nakafuku, Makoto Nishizawa, James Douglas Engel, Masayuki Yamamoto

Research output: Contribution to journalArticlepeer-review

39 Citations (Scopus)

Abstract

Background: Small members of the Maf family of transcriptional regulatory proteins share similar basic-leucine zipper domains but have no intrinsic ability to activate transcription. One member of the family (MafK) has been shown to mediate both negative and positive regulation: in addition to forming a homodimer which represses transcription, MafK can also form a heterodimer with p45 (the large subunit of erythroid transcription factor NF-E2) to activate transcription. Results: We examined the expression of mafK during murine development. mafK mRNA was first detected in 7.5 days post coitus (dpc) embryonic mesoderm and persisted in mesodermal derivatives (mesenchymal and haematopoietic cells) thereafter. However, around 13 dpc mafK. was also strongly induced in neuronal cells and it is broadly expressed in neurones in postnatal mouse. The neuronal expression of mafK is directed by a distinct promoter located 6 kbp 3′ to the mesoderm-specific promoter. mafK in neurones associates with a different partner molecule from p45. In transgenic mice, a regulatory domain in the immediate vicinity of the mesodermal promoter was found to direct mesenchymal, but not haematopoietic, expression of mafK. Conclusion: The cell type- and developmental stage-specific expression of MafK suggests that, in addition to its demonstrated role in erythroid transcriptional regulation, MafK also plays an important regulatory role in other mesodermally and neuroectodermally derived tissues during mouse embryonic development.

Original languageEnglish
Pages (from-to)223-238
Number of pages16
JournalGenes to Cells
Volume1
Issue number2
DOIs
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Genetics
  • Cell Biology

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