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The analysis of chromatin condensation state and transcriptional activity using DNA microarrays

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The DNA microarray-based technique has been developed to semi-quantitatively measure the in vivo global chromatin condensation state at the resolution of a gene. Chromatin was fractionated due to the differential solubility of histone H1-containing and histone H1-free nucleosomes. A set of genes non-randomly distributed between histone H1-free (uncondensed or open) and histone H1-containing (condensed or closed) chromatin fractions has been identified. The transcript levels have been measured for the same group of genes. The correlation between transcriptional activity and chromatin fraction distribution of particular genes has been established.
Rocznik
Tom
Strony
IP13--19
Opis fizyczny
Bibliogr. 5 poz., rys.
Twórcy
autor
  • Department of Experimental and Clinical Radiobiology, Center of Oncology, Gliwice, Poland
  • Department of Automatic Control, Institute of Automation, Silesian Technical University, Gliwice, Poland
Bibliografia
  • [1] WIDLAK P., GARRARD WT., Nucleosomes and regulation of gene expression. Structure of the HIV-1 5’LTR. Acta Biochimica Polonica, vol. 45, pp. 209-219, 1998.
  • [2] CHURCHILL GA., Fundamentals of experimental design for cDNA microarrays. Nature Genetics, supplement, vol. 32, pp. 490-495, 2002.
  • [3] GARRARD WT., Histone H1 and the conformation of transcriptionally active chromatin. Bioessays, vol. 13, pp. 87-88, 1991.
  • [4] HUANG SY., GARRARD WT., Electrophoretic analyses of nucleosomes and other protein-DNA complexes. Methods in Enzymology, vol. 170, pp. 116-142, 1989.
  • [5] POLLACK JR., Parallel analysis of gene copy number and expression using cDNA microarrays. Methods in Molecular Biology, vol. 224, pp. 89-97, 2003.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-PWA4-0020-0002
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