Interaction of the CCAAT displacement protein with shared regulatory elements required for transcription of paired histone genes
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Summary
Analysis of the transcription of histone gene pairs containing deletions and site-specific mutations of intergenic DNA revealed that both promoters are distinct but that they overlap physically and share multiple regulatory elements, providing a possible basis for the coordinate regulation of their in vivo activities.
- Type
- article
- Published
- 1995-07-01
- Cited by
- 55
- References
- 42
- Access
- Open access
- OpenAlex
- https://openalex.org/W1841366287
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:31359115
Keywords
Biology, Promoter, Histone, Genetics, Intergenic region
References
- DNA-binding specificity of the cut repeats from the human cut-like protein
- Genomic organization and nucleotide sequence of two distinct histone gene clusters from Xenopus laevis. Identification of novel conserved upstream sequence elements.
- Directional regulatory activity of cis-acting elements in the bidirectional alpha 1(IV) and alpha 2(IV) collagen gene promoter.
- Biochemical analysis of the B subunit of the heteromeric CCAAT-binding factor. A DNA-binding domain and a subunit interaction domain are specified by two separate segments.
- CCAAT displacement protein as a repressor of the myelomonocytic-specific gp91-phox gene promoter.
- Histone H2B gene transcription during Xenopus early development requires functional cooperation between proteins bound to the CCAAT and octamer motifs
- A variant octamer motif in a Xenopus H2B histone gene promoter is not required for transcription in frog oocytes
- A specific CCAAT-binding protein, CBP/tk, may be involved in the regulation of thymidine kinase gene expression in human IMR-90 diploid fibroblasts during senescence.
- The regulation of histone gene expression during the cell cycle.
- A family of human CCAAT-box-binding proteins active in transcription and DNA replication: cloning and expression of multiple cDNAs
- Mutually exclusive interaction of the CCAAT-binding factor and of a displacement protein with overlapping sequences of a histone gene promoter.
- Principles of medical genetics: By T. D. Gelehrter and F. S. Collins. York, pennsylvania: Williams and Wilkins. (1990). 324 pp. $34.95
- The organization and expression of histone gene families.
- S-phase-specific regulation by deletion mutants of the human thymidine kinase promoter.
- Patterns of expression of cut, a protein required for external sensory organ development in wild-type and cut mutant Drosophila embryos.
- Human CCAAT displacement protein is homologous to the Drosophila homeoprotein, cut
- Primary structure and expression of a product from cut, a locus involved in specifying sensory organ identity in Drosophila
- Individual Xenopus histone genes are replication-independent in oocytes and replication-dependent in Xenopus or mouse somatic cells.
- Cooperation between CCAAT and octamer motifs in the distal sequence element of the rat U3 small nucleolar RNA promoter.
- The E2F transcription factor is a cellular target for the RB protein.
Cited by
- The Aspergillus nidulans multimeric CCAAT binding complex AnCF is negatively autoregulated via its hapB subunit gene.
- Novel basic-region helix-loop-helix transcription factor (AnBH1) of Aspergillus nidulans counteracts the CCAAT-binding complex AnCF in the promoter of a penicillin biosynthesis gene.
- Conserved regulatory elements establish the dynamic expression of Rpx/HesxI in early vertebrate development.
- Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation
- The integrated activities of IRF-2 (HiNF-M), CDP/cut (HiNF-D) and H4TF-2 (HiNF-P) regulate transcription of a cell cycle controlled human histone H4 gene: mechanistic differences between distinct H4 genes
- The CCAAT displacement protein/cut homeodomain protein represses osteocalcin gene transcription and forms complexes with the retinoblastoma protein-related protein p107 and cyclin A.
- The homeodomain transcription factor CDP/cut interacts with the cell cycle regulatory element of histone H4 genes packaged into nucleosomes
- Selective expression of specific histone H4 genes reflects distinctions in transcription factor interactions with divergent H4 promoter elements.
- The human and mouse replication-dependent histone genes.
- Developmentally-regulated interaction of a transcription factor complex containing CDP/cut with the early histone H3 gene promoter of the sea urchin Tetrapygus niger is associated with changes in chromatin structure and gene expression.
- C/EBPɛ mediates myeloid differentiation and is regulated by the CCAAT displacement protein (CDP/cut)
- HAP-Like CCAAT-binding complexes in filamentous fungi: implications for biotechnology.
- Hair defects and pup loss in mice with targeted deletion of the first cut repeat domain of the Cux/CDP homeoprotein gene.
- Role of the multifunctional CDP/Cut/Cux homeodomain transcription factor in regulating differentiation, cell growth and development.
- CCAAT Displacement Activity Involves CUT Repeats 1 and 2, Not the CUT Homeodomain*
- Regulation of murine Tap1 and Lmp2 genes in macrophages by interferon gamma is mediated by STAT1 and IRF-1
- Cux/CDP homeodomain protein binds to an enhancer in the rat c-mos locus and represses its activity.
- Regulation of the homeodomain CCAAT displacement/cut protein function by histone acetyltransferases p300/CREB-binding protein (CBP)-associated factor and CBP.
- The promoter of the rat 5α-reductase type 1 gene is bidirectional and Sp1-dependent
- Evaluation of a potential regulatory role for inverted CCAAT boxes in the human topoisomerase II alpha promoter.
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