PMID- 9160753 OWN - NLM STAT- MEDLINE DCOM- 19970612 LR - 20190705 IS - 0092-8674 (Print) IS - 0092-8674 (Linking) VI - 89 IP - 4 DP - 1997 May 16 TI - Transcription factor Sp1 is essential for early embryonic development but dispensable for cell growth and differentiation. PG - 619-28 AB - 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. FAU - Marin, M AU - Marin M AD - Erasmus University Rotterdam, Department of Cell Biology, The Netherlands. FAU - Karis, A AU - Karis A FAU - Visser, P AU - Visser P FAU - Grosveld, F AU - Grosveld F FAU - Philipsen, S AU - Philipsen S LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Cell JT - Cell JID - 0413066 RN - 0 (DNA Primers) RN - 0 (Sp1 Transcription Factor) SB - IM MH - Animals MH - Base Sequence MH - Cell Differentiation/genetics/physiology MH - Cell Division/genetics/physiology MH - Chimera MH - CpG Islands MH - DNA Methylation MH - DNA Primers/genetics MH - Embryonic and Fetal Development/genetics/*physiology MH - Female MH - Gene Targeting MH - Male MH - Mice MH - Mice, Inbred C57BL MH - Mice, Knockout MH - Pregnancy MH - Sp1 Transcription Factor/genetics/*physiology EDAT- 1997/05/16 00:00 MHDA- 1997/05/16 00:01 CRDT- 1997/05/16 00:00 PHST- 1997/05/16 00:00 [pubmed] PHST- 1997/05/16 00:01 [medline] PHST- 1997/05/16 00:00 [entrez] AID - S0092-8674(00)80243-3 [pii] AID - 10.1016/s0092-8674(00)80243-3 [doi] PST - ppublish SO - Cell. 1997 May 16;89(4):619-28. doi: 10.1016/s0092-8674(00)80243-3.