0000000000429464

AUTHOR

Roberto Gristina

0000-0002-2957-3377

showing 3 related works from this author

Triiodothyronine-Induced Shortening of Chromatin Repeat Length in Neurons Cultured in a Chemically Denned Medium

1987

Abstract: At the time of terminal differentiation, mammalian cortical neurons undergo a dramatic change in the structural organization of their chromatin: the nucleosomal repeat length shortens from ∼200 base pairs in fetuses to a value of 165 base pairs after birth. These events occur several days after the end of neuronal proliferation. Previously, we reported that rat cortical neurons cultured in a very selective synthetic medium were not yet programmed to these events at the end of mitotic cycles. Herein, we report that addition of triiodothyronine to neuronal cultures induces a shortening of the chromatin repeat length comparable to the natural one. Copyright © 1987, Wiley Blackwell. A…

Neuronal terminal differentiationTime FactorsCellular differentiationBiologySettore BIO/19 - Microbiologia GeneraleChromatin structureBiochemistryCellular and Molecular NeuroscienceSettore BIO/10 - BiochimicamedicineAnimalsNucleosomeMitosisCells CulturedCerebral CortexNeuronsGeneticsNucleosomal Repeat LengthTriiodothyronineDNAChromatinCulture MediaRatsChromatinCell biologyChemically denned medium)Chemically defined mediummedicine.anatomical_structurenervous systemTriiodothyronineSettore MED/26 - NeurologiaNeuronJournal of Neurochemistry
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Cloning and analysis of cDNA for rat histone H1°

1993

Regulation of gene expressionCloningbiologyCellular differentiationMolecular cloningMolecular biologychemistry.chemical_compoundHistonechemistryHistone H1Complementary DNAGeneticsbiology.proteinDNANucleic Acids Research
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The dynamic properties of neuronal chromatin are modulated by triiodothyronine.

1992

The effect of triiodothyronine (T3) on the rate of synthesis of nuclear proteins was studied during terminal differentiation of rat cortical neurons cultured in a serum-free medium. To this aim total and acid soluble nuclear proteins were analyzed by different electrophoretic techniques. Our results show that: 1) during maturation in vitro, neuronal nuclei undergo a dramatic change in the rate at which different classes of histones and high mobility group (HMG) proteins are synthesized; the synthetic activity, measured as incorporation of radioactive precursors into nuclear proteins, slows indeed down with age: especially evident is the decrease in core histones synthesis; at day 15, on the…

CNS developmentLysineBiologyBiochemistryCellular and Molecular NeuroscienceSettore BIO/10 - BiochimicamedicineAnimalsSettore BIO/06 - Anatomia Comparata E CitologiaNuclear proteinCells CulturedNeuronsTriiodothyronineLysineGeneral MedicineneuronChromatinChromatinCell biologyRatsCell nucleusmedicine.anatomical_structureHigh-mobility groupHistoneBiochemistrySolubilitybiology.proteinTriiodothyronineSettore MED/26 - NeurologiaElectrophoresis Polyacrylamide GelNeuronNeurochemical research
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