Transcription factor Sp1 is essential for early embryonic development but dispensable for cell growth and differentiation.
January 1997
Article
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Transcription factor Sp1 has been implicated in the expression of many genes. Moreover, it has been suggested that Sp1 is linked to the maintenance of methylation-free CpG islands, the cell cycle, and the formation of active chromatin structures. We have inactivated the mouse Sp1 gene. Sp1-/- embryos are retarded in development, show a broad range of abnormalities, and die around day 11 of gestation. In Sp1-/- embryos, the expression of many putative target genes, including cell cycle-regulated genes, is not affected, CpG islands remain methylation free, and active chromatin is formed at the globin loci. However, the expression of the methyl-CpG-binding protein MeCP2 is greatly reduced in Sp1-/- embryos. MeCP2 is thought to be required for the maintenance of differentiated cells. We suggest that Sp1 is an important regulator of this process.
- Male
- Animals
- Support, Non-U.S. Gov't
- Female
- Mice
- Base Sequence
- 0 (Transcription Factor, Sp1)
- Mice, Knockout
- DNA Methylation
- Mice, Inbred C57BL
- Pregnancy
- Chimera
- 0 (DNA Primers)
- DNA Primers/genetics
- Gene Targeting
- Embryo and Fetal Development/genetics/*physiology
- Cell Division/genetics/physiology
- Cell Differentiation/genetics/physiology
- CpG Islands
- Transcription Factor, Sp1/genetics/*physiology
- embryo
- figure
- protein
- expression
- island
- / embryos
- mecp 2
- sp 1 gene
- methylation
- mouse
- mecp 2 protein
- cpg islands
- / es cells
- development
- binding
- analysis
- es cells
- transcription
- hpaii
- aprt gene