Abstract:We report the cloning of Xenopus laevis Xsap-1 cDNA, encoding a member of the ternary complex factor subfamily of ETS transcription factors. The expression pattern of Xsap-1 was examined during Xenopus embryogenesis using whole-mount in situ hybridization. Spatial expression of Xsap-1 mRNA is first detected at the animal pole at the mid-blastula stage. During neurulation Xsap-1 is expressed in cells participating in neural tube formation, in the sensorial layer of the epidermal ectoderm, and in an anterior reg… Show more
“…Several regulatory serum response elements (SREs) are clustered near its core promoter region (16,17) that are bound cooperatively by the MADS box protein serum response factor (SRF) and one member of the ternary complex factor (TCF) family that includes ELK1, SAP1 (SRF accessory protein-1), and NET [new ets (E twenty-six) factor] (18). Orthologous TCF factors are expressed in humans and mice, and similar factors have been identified in Xenopus and zebrafish (19)(20)(21). These TCFs constitute a subfamily of the larger ets superfamily of DNA binding transcription factors (22).…”
Transcript elongation by polymerase II paused at the Egr1 promoter is activated by mitogen-activated protein kinase phosphorylation of the ternary complex factor (TCF) ELK1 bound at multiple upstream sites and subsequent phospho-ELK1 interaction with mediator through the MED23 subunit. Consequently, Med23 knockout (KO) nearly eliminates Egr1 (early growth response factor 1) transcription in embryonic stem (ES) cells, leaving a paused polymerase at the promoter. Med23 KO did not, however, eliminate Egr1 transcription in fibroblasts. Chromatin immunoprecipitation analysis and direct visualization of fluorescently labeled TCF derivatives and mediator subunits revealed that three closely related TCFs bound to the same control regions. The relative amounts of these TCFs, which responded differently to the loss of MED23, differed in ES cells and fibroblasts. Transcriptome analysis suggests that most genes expressed in both cell types, such as Egr1, are regulated by alternative transcription factors in the two cell types that respond differently to the same signal transduction pathways.
“…Several regulatory serum response elements (SREs) are clustered near its core promoter region (16,17) that are bound cooperatively by the MADS box protein serum response factor (SRF) and one member of the ternary complex factor (TCF) family that includes ELK1, SAP1 (SRF accessory protein-1), and NET [new ets (E twenty-six) factor] (18). Orthologous TCF factors are expressed in humans and mice, and similar factors have been identified in Xenopus and zebrafish (19)(20)(21). These TCFs constitute a subfamily of the larger ets superfamily of DNA binding transcription factors (22).…”
Transcript elongation by polymerase II paused at the Egr1 promoter is activated by mitogen-activated protein kinase phosphorylation of the ternary complex factor (TCF) ELK1 bound at multiple upstream sites and subsequent phospho-ELK1 interaction with mediator through the MED23 subunit. Consequently, Med23 knockout (KO) nearly eliminates Egr1 (early growth response factor 1) transcription in embryonic stem (ES) cells, leaving a paused polymerase at the promoter. Med23 KO did not, however, eliminate Egr1 transcription in fibroblasts. Chromatin immunoprecipitation analysis and direct visualization of fluorescently labeled TCF derivatives and mediator subunits revealed that three closely related TCFs bound to the same control regions. The relative amounts of these TCFs, which responded differently to the loss of MED23, differed in ES cells and fibroblasts. Transcriptome analysis suggests that most genes expressed in both cell types, such as Egr1, are regulated by alternative transcription factors in the two cell types that respond differently to the same signal transduction pathways.
“…A second human elk-1 chromosomal location was first described as the elk-2 locus (Rao et al, 1989), but has finally been shown to correspond to two elk-1-related processed pseudogenes embedded in the IgH locus (Harindranath et al, 1998). TCF like factors have been identified in Xenopus, (Nentwich et al, 2001), Goldfish (Goldman et al, 1998), Zebrafish (Brown et al, 1999) and Caenorhabditis elegans (Beitel et al, 1995).…”
“…In Xenopus, zebrafish and chick, Ets expression is initiated in premigratory crest, while Twist comes on in early migrating crest [33,[38][39][40][41]. In lamprey, four homologues of Twist and three of Ets have been identified; all of these genes are expressed in postmigratory crest cells [32].…”
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