2000
DOI: 10.1074/jbc.275.17.12879
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The Zinc Finger Repressor, ZBP-89, Binds to the Silencer Element of the Human Vimentin Gene and Complexes with the Transcriptional Activator, Sp1

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Cited by 60 publications
(100 citation statements)
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“…Mutation of this sequence within À261/ þ 72CAT resulted in little reporter gene activity, which did not increase with the inclusion of additional 5 0 -end DNA up to position À1114 (Izmailova et al, 1999a). Other DNA elements include a TATA box, a PEA3 site (Chen et al, 1996), an NF-kB element (Lilienbaum and Paulin, 1993), a proximal silencer (PS), which binds the repressor protein ZBP-89 (Wieczorek et al, 2000), and an antisilencer element (ASE) (Izmailova and Zehner, 1999b).…”
Section: Localization Of Dna Sequences Required For C-jun Induction Omentioning
confidence: 99%
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“…Mutation of this sequence within À261/ þ 72CAT resulted in little reporter gene activity, which did not increase with the inclusion of additional 5 0 -end DNA up to position À1114 (Izmailova et al, 1999a). Other DNA elements include a TATA box, a PEA3 site (Chen et al, 1996), an NF-kB element (Lilienbaum and Paulin, 1993), a proximal silencer (PS), which binds the repressor protein ZBP-89 (Wieczorek et al, 2000), and an antisilencer element (ASE) (Izmailova and Zehner, 1999b).…”
Section: Localization Of Dna Sequences Required For C-jun Induction Omentioning
confidence: 99%
“…Various 5 0 -deletion constructs À757/ þ 72, À353/ þ 72, or À261/ þ 72 and site-mutated constructs (À353/ þ 72mNF-kB, À353/ þ 72mPEA3, À353/ þ 72mSp1) of the human vimentin promoter were fused to the CAT gene as previously described (Wieczorek et al, 2000;Zhang et al, 2003). The pCMV-c-Jun plasmid and the various mutants (TAM67, DBM-3, and LZM-1) were kindly provided by Dr Michael Birrer (NCI/NIH), pCMV-Sp1 by Dr Juanita Merchant (University of Michigan), pPac-b-gal, pPacSp1, and the various deletion constructs of Sp1 by Dr Robert Tjian (UC-Berkeley), and pPac-c-Jun by Dr John Noti (Guthrie Res.…”
Section: Plasmidsmentioning
confidence: 99%
“…Mt␤ (identical to BFCOL1, BERF-1) and its human and rat homologues (ht␤, ZBP-89, ZFP148) are reported to bind regulatory regions of various genes, such as the V␤8.1 promoter and the V␣ silencer of the T-cell receptor genes (17), the gastrin promoter (29), the type I collagen promoter (27), the ␤-enolase enhancer (28), the ornithine decarboxylase promoter (30), the p21WAF1 promoter (31), the matrix metalloproteinase-3 promoter (32), the pT␣ enhancer (33), and the silencer element of the vimentin gene (34). Our data showing that mt␤ is ubiquitously expressed at both mRNA and protein levels are consistent with previously published reports and the fact that mt␤ functions in the various promoters and enhancers in various tissues.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, the binding site of mt␤ appears to be important for the pT␣ enhancer element (33). In contrast, mt␤ represses transcription from the gastrin gene (29), the ␤-enolase gene (28), the ornithine decarboxylase gene (30), and the vimentin gene (34). It is currently unknown how mt␤/BFCOL1/BERF-1 (ht␤/ZBP-89/ZFP148 in humans) manifests opposite activities on transcription of different genes.…”
Section: Discussionmentioning
confidence: 99%
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