RESUMO
Adhesion-G protein-coupled receptors (GPCRs) are a poorly studied subgroup of the GPCRs, which have diverse biological roles and are major targets for therapeutic intervention. Among them, the Brain Angiogenesis Inhibitor (BAI) family has been linked to several psychiatric disorders, but despite their very high neuronal expression, the function of these receptors in the central nervous system has barely been analyzed. Our results, obtained using expression knockdown and overexpression experiments, reveal that the BAI3 receptor controls dendritic arborization growth and branching in cultured neurons. This role is confirmed in Purkinje cells in vivo using specific expression of a deficient BAI3 protein in transgenic mice, as well as lentivirus driven knockdown of BAI3 expression. Regulation of dendrite morphogenesis by BAI3 involves activation of the RhoGTPase Rac1 and the binding to a functional ELMO1, a critical Rac1 regulator. Thus, activation of the BAI3 signaling pathway could lead to direct reorganization of the actin cytoskeleton through RhoGTPase signaling in neurons. Given the direct link between RhoGTPase/actin signaling pathways, neuronal morphogenesis and psychiatric disorders, our mechanistic data show the importance of further studying the role of the BAI adhesion-GPCRs to understand the pathophysiology of such brain diseases.
Assuntos
Dendritos/fisiologia , Proteínas do Tecido Nervoso/fisiologia , Neurogênese/fisiologia , Proteínas Adaptadoras de Transdução de Sinal/metabolismo , Animais , Células Cultivadas , Dendritos/ultraestrutura , Técnicas de Silenciamento de Genes , Proteínas de Membrana , Camundongos , Camundongos Transgênicos , Proteínas do Tecido Nervoso/genética , Neurogênese/genética , Células de Purkinje/fisiologia , Células de Purkinje/ultraestrutura , Transdução de Sinais/fisiologiaRESUMO
Genetic analysis in mice has most commonly employed two general strategies: phenotypic screens for spontaneous or induced mutations and genotypic analysis using homologous recombination or gene trapping to produce deletion or insertion mutants. Here we use bacterial artificial chromosome (BAC)-mediated gene-dosage analysis in transgenic mice to reveal novel genetic functions that are not evident from conventional loss-of-function mutations. We demonstrate a role for the zinc-finger transcription factor Zipro1 (formerly Ru49 and Zfp38) in the proliferation of granule cell precursors in the developing cerebellum, and document the contribution of this process to the final stages of cerebellar morphogenesis. We also show that Zipro1 is expressed in skin, and increased Zipro1 dosage results in a hair-loss phenotype associated with increased epithelial cell proliferation and abnormal hair follicle development.
Assuntos
Cerebelo/citologia , Cromossomos Bacterianos , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/fisiologia , Dosagem de Genes , Pele/citologia , Células-Tronco/metabolismo , Transativadores/genética , Transativadores/fisiologia , Animais , Contagem de Células , Morte Celular , Divisão Celular , Cerebelo/anatomia & histologia , Proteínas de Ligação a DNA/análise , Proteínas de Ligação a DNA/metabolismo , Técnicas Genéticas , Cabelo/metabolismo , Camundongos , Camundongos Transgênicos , Modelos Genéticos , Fenótipo , Transativadores/análise , Transativadores/metabolismoRESUMO
The treatment of axonal disorders, such as diseases associated with axonal injury and degeneration, is limited by the inability to directly target therapeutic protein expression to injured axons. Current gene therapy approaches rely on infection and transcription of viral genes in the cell body. Here, we describe an approach to target gene expression selectively to axons. Using a genetically engineered mouse containing epitope-labeled ribosomes, we find that neurons in adult animals contain ribosomes in distal axons. To use axonal ribosomes to alter local protein expression, we utilized a Sindbis virus containing an RNA genome that has been modified so that it can be directly used as a template for translation. Selective application of this virus to axons leads to local translation of heterologous proteins. Furthermore, we demonstrate that selective axonal protein expression can be used to modify axonal signaling in cultured neurons, enabling axons to grow over inhibitory substrates typically encountered following axonal injury. We also show that this viral approach also can be used to achieve heterologous expression in axons of living animals, indicating that this approach can be used to alter the axonal proteome in vivo. Together, these data identify a novel strategy to manipulate protein expression in axons, and provides a novel approach for using gene therapies for disorders of axonal function.
Assuntos
Axônios/fisiologia , Marcação de Genes/métodos , Vetores Genéticos , Sindbis virus/genética , Adenilil Ciclases/genética , Animais , Axônios/metabolismo , Camundongos , Regeneração Nervosa , Ribossomos/virologia , Medula EspinalRESUMO
Initiation of DNA replication is mediated by the assembly of nucleoprotein complexes at cis-acting DNA sequences known as origins of replication. Recent studies in several systems show that accessory transcription factors accentuate origin utilization by multiple mechanisms. The remarkable similarities in the activities of accessory transcription factors at promoters and origins of replication suggest that transcription factors play a pivotal role in the regulation of chromosomal DNA synthesis in eukaryotic organisms.
Assuntos
Replicação do DNA/fisiologia , Fatores de Transcrição/fisiologia , Animais , Cromatina/metabolismo , Células Eucarióticas/metabolismo , Modelos Biológicos , Conformação de Ácido Nucleico , Nucleoproteínas/metabolismo , Saccharomyces cerevisiae/metabolismoRESUMO
The expression of a hsp70 gene in human cells has previously been shown to be related to the growth state of the cells. As an alternative to in vitro synchronization procedures, we have measured steady-state levels of the RNA for a heat-shock protein 70 (hsp70) in human peripheral blood mononuclear cells (PBMC) that are naturally quiescent in a G0 state. The probe used recognized, on RNA blots, one single band. The levels of this hsp70 RNA are elevated in circulating PBMC and decrease when the cells are incubated with serum, or phytohemagglutinin, or simply when they are incubated in culture medium. The levels of hsp70 RNA decrease within 30 min after in vitro culture, and are accompanied by an increase in the levels of c-fos RNA. These findings, together with other recent reports in the literature, suggest a possible role of the hsp70 proteins in the regulation of cell growth.
Assuntos
Genes , Proteínas de Choque Térmico/genética , Oncogenes , RNA Mensageiro/genética , Linfócitos T/metabolismo , Transcrição Gênica , Linhagem Celular , Transformação Celular Neoplásica , Humanos , Acetato de Tetradecanoilforbol/farmacologiaRESUMO
Orderly progression through the somatic cell division cycle is accompanied by phase-specific transcription of a variety of different genes. During S phase, transcription of mammalian histone H2B genes requires a specific promoter element and its cognate transcription factor Oct1 (OTF1). A possible mechanism for regulating histone H2B transcription during the cell cycle is direct modulation of Oct1 activity by phase-specific posttranslational modifications. Analysis of Oct1 during progression through the cell cycle revealed a complex temporal program of phosphorylation. A p34cdc2-related protein kinase that is active during mitosis may be responsible for one mitotic phosphorylation of Oct1. However, the temporally controlled appearance of Oct1 phosphopeptides suggests the involvement of multiple kinases and phosphatases. These results support the idea that cell cycle-regulated transcription factors may be direct substrates for phase-specific regulatory enzymes.
Assuntos
Ciclo Celular , Proteínas de Ligação a DNA/metabolismo , Fatores de Transcrição/metabolismo , Proteína Quinase CDC2/metabolismo , Proteínas de Ligação a DNA/isolamento & purificação , Células HeLa/citologia , Células HeLa/fisiologia , Histonas/genética , Fator C1 de Célula Hospedeira , Humanos , Mitose , Fator 1 de Transcrição de Octâmero , Mapeamento de Peptídeos , Fosfopeptídeos/isolamento & purificação , Fosforilação , Fase S , Fatores de Transcrição/isolamento & purificaçãoRESUMO
Oct-1 is a transcription factor involved in the cell cycle regulation of histone H2B gene transcription and in the transcription of other cellular housekeeping genes. Oct-1 is hyperphosphorylated as cells enter mitosis, and mitosis-specific phosphorylation is reversed as cells exit mitosis. A mitosis-specific phosphorylation site in the homeodomain of Oct-1 was phosphorylated in vitro by protein kinase A. Phosphorylation of this site correlated with inhibition of Oct-1 DNA binding activity in vivo and in vitro. The inhibition of Oct-1 DNA binding during mitosis suggests a mechanism by which the general inhibition of transcription during mitosis might occur.
Assuntos
Proteínas de Ligação a DNA/metabolismo , Fatores de Transcrição/metabolismo , Sequência de Aminoácidos , Animais , Sequência de Bases , Bovinos , Ciclo Celular , Clonagem Molecular , DNA de Neoplasias/metabolismo , Proteínas de Ligação a DNA/genética , Genes Homeobox , Células HeLa , Histonas/genética , Fator C1 de Célula Hospedeira , Humanos , Mitose , Dados de Sequência Molecular , Miocárdio/enzimologia , Fator 1 de Transcrição de Octâmero , Oligodesoxirribonucleotídeos , Mapeamento de Peptídeos , Fosfopeptídeos/isolamento & purificação , Fosforilação , Proteínas Quinases/metabolismo , Fatores de Transcrição/genéticaRESUMO
Vertebrate central nervous system (CNS) histogenesis depends on glia-guided migration of postmitotic neurons to form neuronal laminae. Previous studies have established that the neuronal protein astrotactin functions in murine cerebellar granule cell migration in vitro. The gene encoding astrotactin predicts a protein with three epidermal growth factor repeats and two fibronectin type III repeats. Astrotactin messenger RNA is expressed in postmitotic neuronal precursors in the cerebellum, hippocampus, cerebrum, and olfactory bulb, where migration establishes laminar structures. Fab fragments of antibodies to a recombinant astrotactin peptide blocked migration of cerebellar granule neurons in vitro along astroglial fibers. Transfection of astrotactin complementary DNA into 3T3 cells indicated that astrotactin acts as a ligand for neuron-glia binding during neuronal migration.
Assuntos
Encéfalo/metabolismo , Glicoproteínas/genética , Glicoproteínas/fisiologia , Proteínas do Tecido Nervoso/genética , Proteínas do Tecido Nervoso/fisiologia , Neuroglia/metabolismo , Neurônios/fisiologia , Células 3T3 , Sequência de Aminoácidos , Animais , Astrócitos/metabolismo , Northern Blotting , Movimento Celular , Cerebelo/citologia , Cerebelo/metabolismo , Expressão Gênica , Glicoproteínas/química , Hipocampo/metabolismo , Ligantes , Camundongos , Dados de Sequência Molecular , Proteínas do Tecido Nervoso/química , Neurônios/citologia , Bulbo Olfatório/metabolismo , TransfecçãoRESUMO
Octamer transcription factor-1 (OTF-1) and nuclear factor III (NF-III) are sequence-specific DNA binding proteins that activate transcription and DNA replication, respectively. It is shown here that OTF-1 is physically and biologically indistinguishable from NF-III. This conclusion is based on the following observations. First, the two proteins have identical mobilities by SDS-polyacrylamide gel electrophoresis. Second, OTF-1 binds to the adenovirus origin of DNA replication at the same site and with the same affinity as NF-III. Third, OTF-1 can substitute for NF-III in activating the initiation of adenovirus DNA replication in vitro. Fourth, the ability of OTF-1 to stimulate viral DNA replication is dependent on the presence of an intact NF-III binding site within the origin of replication. Fifth, NF-III can substitute for OTF-1 in activating in vitro transcription from the human histone H2b promoter. These data suggest the possibility that NF-III/OTF-1 is a protein that functions in both cellular DNA replication and transcription.
Assuntos
Replicação do DNA/efeitos dos fármacos , Proteínas de Ligação a DNA/farmacologia , Proteínas Nucleares/farmacologia , Fatores de Transcrição/farmacologia , Transcrição Gênica/efeitos dos fármacos , Adenoviridae/fisiologia , Proteínas de Ligação a DNA/metabolismo , Eletroforese em Gel de Poliacrilamida , Células HeLa , Histonas/genética , Fator C1 de Célula Hospedeira , Humanos , Peso Molecular , Proteínas Nucleares/metabolismo , Fator 1 de Transcrição de Octâmero , Regiões Promotoras Genéticas , Fatores de Transcrição/metabolismo , Replicação Viral/efeitos dos fármacosRESUMO
Cell-cycle-regulated transcription is a characteristic feature of complex cell cycles in organisms as divergent as yeasts and humans. Increasing evidence suggests that transcriptional regulation may control key events in the eukaryotic cell cycle. In this review we will address the mechanisms that may regulate transcription during the cell cycle and the roles which periodic transcription may serve in the control of cell cycle progression.
Assuntos
Ciclo Celular/genética , Regulação da Expressão Gênica , Transcrição Gênica , Saccharomyces/genéticaRESUMO
Using a polyclonal antibody against postnatal cerebellar cells, we have isolated a new, brain-specific member of the lipid-binding protein family (BLBP). Members of this family, such as cellular retinoic acid-binding protein, have been shown to carry small hydrophobic signaling molecules between cellular compartments. The expression of BLBP is spatially and temporally correlated with neuronal differentiation in many parts of the mouse CNS, including postnatal cerebellum, embryonic spinal cord, and cerebral cortex. In situ hybridization and immunocytochemistry show that BLBP is transiently expressed in radial glia in both the embryonic ventricular zone and the postnatal cerebellum. Subcellular localization studies by immunoelectron microscopy demonstrate that BLBP is present in the nucleus as well as the cytoplasm. Affinity-purified anti-BLBP antibodies block glial and neuronal differentiation in primary cell cultures, but have no effect on cell proliferation or adhesion. Based on these results, we propose that BLBP is required for the establishment of the radial glial fiber system in developing brain, a system that is necessary for the migration of immature neurons to establish cortical layers.
Assuntos
Proteínas de Transporte/fisiologia , Cerebelo/crescimento & desenvolvimento , Proteínas do Tecido Nervoso/fisiologia , Transdução de Sinais , Sequência de Aminoácidos , Animais , Anticorpos/farmacologia , Sequência de Bases , Proteínas de Transporte/imunologia , Diferenciação Celular/efeitos dos fármacos , Células Cultivadas , Cerebelo/química , Córtex Cerebral/química , Córtex Cerebral/embriologia , Proteína 7 de Ligação a Ácidos Graxos , Proteínas de Ligação a Ácido Graxo , Imuno-Histoquímica , Hibridização In Situ , Camundongos , Microscopia Imunoeletrônica , Dados de Sequência Molecular , Proteínas do Tecido Nervoso/imunologia , Neuroglia/citologia , Neurônios/citologia , Medula Espinal/química , Medula Espinal/embriologiaRESUMO
When CNS precursor cells purified from the external germinal layer of the early postnatal mouse cerebellum are cultured in cellular reaggregates, DNA synthesis increased 10-fold above that of cells dispersed in a monolayer or embedded in a collagen matrix. Dividing precursor cells gave rise to neurons immunopositive for the neural antigens N-CAM, L1, and TAG-1, but not to astroglial cells immunopositive for glial filament protein. Moreover, proliferating precursor cells did not generate other types of cerebellar neurons, as judged by the lack of expression of glutamic acid decarboxylase, the synthetic enzyme for gamma-amino-n-butyric acid. By contrast, the addition of astroglial cells, or astroglial cell membranes, to cellular reaggregates of granule cell neuroblasts arrested precursor cell DNA synthesis in a dose-dependent manner. These results suggest that homotypic contact interactions among CNS neural progenitors control precursor cell proliferation and fate in generative zones of developing brain.
Assuntos
Comunicação Celular/fisiologia , Divisão Celular/fisiologia , Cerebelo/citologia , Neurônios/fisiologia , Aminobutiratos/metabolismo , Animais , Astrócitos/enzimologia , Astrócitos/fisiologia , Células Cultivadas , Cerebelo/embriologia , Colágeno/fisiologia , DNA/biossíntese , Glutamato Descarboxilase/genética , Técnicas In Vitro , Camundongos , Neuroglia/enzimologia , Neuroglia/fisiologia , Neurônios/enzimologiaRESUMO
Elapid snake venom neurotoxins exert their effects through high-affinity interactions with specific neurotransmitter receptors. A novel murine gene, lynx1, is highly expressed in the brain and contains the cysteine-rich motif characteristic of this class of neurotoxins. Primary sequence and gene structure analyses reveal an evolutionary relationship between lynx1 and the Ly-6/neurotoxin gene family. lynx1 is expressed in large projection neurons in the hippocampus, cortex, and cerebellum. In cerebellar neurons, lynx1 protein is localized to a specific subdomain including the soma and proximal dendrites. lynx1 binding to brain sections correlates with the distribution of nAChRs, and application of lynx1 to Xenopus oocytes expressing nAChRs results in an increase in acetylcholine-evoked macroscopic currents. These results identify lynx1 as a novel protein modulator for nAChRs in vitro, which could have important implications in the regulation of cholinergic function in vivo.
Assuntos
Sistema Nervoso Central/metabolismo , Glicoproteínas de Membrana/fisiologia , Neuropeptídeos/fisiologia , Receptores Nicotínicos/metabolismo , Proteínas Adaptadoras de Transdução de Sinal , Sequência de Aminoácidos/genética , Animais , Bungarotoxinas/genética , Sistema Nervoso Central/citologia , Feminino , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/metabolismo , Camundongos , Dados de Sequência Molecular , Família Multigênica/genética , Neurônios/metabolismo , Neuropeptídeos/genética , Neuropeptídeos/metabolismo , Oócitos , XenopusRESUMO
Recent work in yeast shows that eukaryotic origins of DNA replication are multipartite regulatory elements resembling promoters of transcription. As for the regulation of transcription, accessory transcription factors appear to function in concert with basic origin recognition factors to regulate initiation of DNA synthesis at specific subsets of origins. The participation of transcription factors in the regulation of DNA replication may facilitate temporal control of transcription and replication during the cell cycle, as well as providing a mechanism for integrating origin selection with the cellular transcriptional program.
Assuntos
DNA Fúngico/genética , Células Eucarióticas/fisiologia , Replicon , Saccharomyces cerevisiae/genética , Análise Mutacional de DNA , Regulação da Expressão Gênica , Sequências Reguladoras de Ácido Nucleico , Transcrição GênicaRESUMO
H1TF2 is a CCAAT transcription factor that binds to the histone H1 subtype-specific consensus sequence, which has previously been shown to be necessary for temporal regulation of histone H1 transcription during the cell cycle (F. La Bella, P. Gallinari, J. McKinney, and N. Heintz, Genes Dev. 3:1982-1990, 1989). In this study, we report that H1TF2 is a heteromeric CCAAT-binding protein composed of two polypeptide doublets of 33 and 34 kDa and 43 and 44 kDa that are not antigenically related. The 33- and 34-kDa species were not detected in our previous studies (P. Gallinari, F. La Bella, and N. Heintz, Mol. Cell. Biol. 9:1566-1575, 1989) because of technical problems in detection of these heavily glycosylated subunits. The cloning of H1TF2A, the large subunit of this factor, reveals it to be a glutamine-rich protein with extremely limited similarity to previously cloned CCAAT-binding proteins. A monospecific antiserum produced against bacterially synthesized H1TF2A was used to establish that HeLa cell H1TF2A is phosphorylated in vivo and that, in contrast to the H2b transcription factor Oct1 (S. B. Roberts, N. Segil, and N. Heintz, Science 253:1022-1026, 1991; N. Segil, S. B. Roberts, and N. Heintz, Cold Spring Harbor Symp. Quant. Biol. 56:285-292, 1991), no gross change in H1TF2A phosphorylation is evident during the cell cycle. Further immunoprecipitation studies demonstrated that H1TF2 is heterodimeric in the absence of DNA in vivo and identified several H1TF2-interacting proteins that may play a role in H1TF2 function in vivo.
Assuntos
Proteínas Estimuladoras de Ligação a CCAAT , Ciclo Celular , Proteínas de Ligação a DNA/genética , Proteínas de Ligação a DNA/metabolismo , Histonas/fisiologia , Fatores de Transcrição/metabolismo , Sequência de Aminoácidos , Sequência de Bases , Fator de Ligação a CCAAT , Clonagem Molecular , Expressão Gênica , Genes , Células HeLa , Humanos , Substâncias Macromoleculares , Dados de Sequência Molecular , Peso Molecular , Proteínas RecombinantesRESUMO
Replication of the Chinese hamster dihydrofolate reductase gene (dhfr) initiates near a fragment of stably bent DNA that binds multiple cellular factors. Investigation of protein interactions with the dhfr bent DNA sequences revealed a novel nuclear protein that also binds to domain B of the yeast origin of replication, the autonomously replicating sequence ARS1. The origin-specific DNA-binding activity was purified 9,000-fold from HeLa cell nuclear extract in five chromatographic steps. Protein-DNA cross-linking experiments showed that a 60-kDa polypeptide, which we call RIP60, contained the origin-specific DNA-binding activity. Oligonucleotide displacement assays showed that highly purified fractions of RIP60 also contained an ATP-dependent DNA helicase activity. Covalent radiolabeling with ATP indicated that the DNA helicase activity resided in a 100-kDa polypeptide, RIP100. The cofractionation of an ATP-dependent DNA helicase with an origin-specific DNA-binding activity suggests that RIP60 and RIP100 may be involved in initiation of chromosomal DNA synthesis in mammalian cells.
Assuntos
Adenosina Trifosfatases/isolamento & purificação , DNA Helicases/isolamento & purificação , Proteínas de Ligação a DNA/isolamento & purificação , Adenosina Trifosfatases/metabolismo , Trifosfato de Adenosina/metabolismo , Animais , Sequência de Bases , Linhagem Celular , Núcleo Celular/metabolismo , DNA/genética , DNA/metabolismo , DNA Helicases/metabolismo , Proteínas de Ligação a DNA/metabolismo , Desoxirribonuclease I , Células HeLa/metabolismo , Humanos , Dados de Sequência Molecular , Mapeamento de Nucleotídeos , Ligação Proteica , Mapeamento por Restrição , Tetra-Hidrofolato Desidrogenase/genéticaRESUMO
Transcriptional regulation of mammalian histone genes during S phase is achieved through activation of specific factors which interact with subtype-specific histone gene promoter sequences. It has previously been shown that in HeLa cells this induction is not mediated by obligatory changes in the DNA binding activity of histone gene transcription factors as cells progress through the cell cycle. Recently, it has been reported that the DNA binding properties of a putative histone gene transcription factor may be quite different in normal and transformed cells (J. Holthuis, T. A. Owen, A. J. van Wijnen, K. L. Wright, A. Ramsey-Ewing, M. B. Kennedy, R. Carter, S. C. Cosenza, K. J. Soprano, J. B. Lian, J. L. Stein, and G. S. Stein, Science 247:1454-1457, 1990). To determine whether the properties of well-characterized histone gene transcription factors are altered in transformed versus normal cells, we have examined the DNA binding activity of human histone transcription factors during the WI38 (a primary line of normal human fetal lung fibroblasts) cell cycle. The results demonstrate that the properties of Oct1, H4TF1, and H4TF2 are similar in WI38 and HeLa cells and that their DNA binding activities are constitutive during interphase of both normal and transformed cell lines. Although it remains possible that these factors are directly or indirectly perturbed as a result of cellular transformation, it appears unlikely that transformation results in gross changes in DNA binding activity as cells progress toward division.
Assuntos
Histonas/genética , Fatores de Transcrição/metabolismo , Western Blotting , Ciclo Celular , Linhagem Celular , DNA/metabolismo , Proteínas de Ligação a DNA/metabolismo , Fator C1 de Célula Hospedeira , Humanos , Fator 1 de Transcrição de OctâmeroRESUMO
Definition of mechanisms regulating human histone H1 gene transcription during the cell cycle requires the isolation and biochemical characterization of protein factors which interact with specific promoter elements. Two distinct binding activities have been identified in nuclear extracts from HeLa cells and mapped within a 180-base-pair (bp) region of a cell cycle-regulated H1 gene promoter. H1TF1 bound to an H1-specific A + C-rich sequence (AC box), 100 bp upstream of the cap site; H1TF2 interacted with the H1 subtype-specific consensus element and was dependent on the presence of an intact CCAAT box for binding. H1TF2 was purified through a combination of ion-exchange and oligonucleotide affinity chromatographies. Analysis of purified fractions by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and UV crosslinking showed that H1TF2 was a single polypeptide of 47 kilodaltons. This factor was distinct from previously characterized CCAAT-binding proteins in both molecular size and binding properties. Fractions containing H1TF2 activity activated transcription in vitro only if programmed with an H1 DNA template carrying an intact H1TF2-binding site.
Assuntos
Proteínas de Ligação a DNA/isolamento & purificação , Histonas/metabolismo , Sítios de Ligação , Linhagem Celular , Proteínas de Ligação a DNA/metabolismo , Desoxirribonucleotídeos/metabolismo , Regulação da Expressão Gênica , Histonas/genética , Humanos , Regiões Promotoras Genéticas , Transcrição GênicaRESUMO
Specific DNA-binding and in vitro transcription activities of H4TF-1 and H4TF-2 are inactivated by chelating agents. Binding activity is restored by addition of Zn2+, and H4TF-2 is also reactivated by Fe2+. In contrast, preformed factor-DNA complexes are resistant to chelators. Therefore, metal ions are a required component of the H4TF-1 and H4TF-2 DNA-binding domains.