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. 1984 Sep;3(9):2015-20.
doi: 10.1002/j.1460-2075.1984.tb02084.x.

Tissue-specific DNaseI hypersensitive sites in the 5'-flanking sequences of the tryptophan oxygenase and the tyrosine aminotransferase genes

Tissue-specific DNaseI hypersensitive sites in the 5'-flanking sequences of the tryptophan oxygenase and the tyrosine aminotransferase genes

P Becker et al. EMBO J. 1984 Sep.

Abstract

The genes for tryptophan oxygenase (TO) and tyrosine aminotransferase (TAT) are expressed in a tissue- and development-specific manner and are regulated by glucocorticoids (TO and TAT) and glucagon or its intracellular mediator cAMP (TAT) in rat liver. We have analyzed the chromatin structure of these genes in the vicinity of the 5' ends with regard to DNaseI hypersensitivity and have found DNaseI hypersensitive sites upstream of each of the promoters. Mapping of this region reveals three closely spaced cleavage sites near the TO promoter and a doublet of sites near the TAT promoter. In both genes additional cleavage sites are found further upstream. All hypersensitive sites of both genes are absent in kidney nuclei and therefore appear to be specific for the tissue expressing the genes. A correlation of expression and modified chromatin structure was also observed in a hepatoma cell line expressing TAT but not TO: hypersensitive sites are present in TAT but not in TO chromatin. Upon glucocorticoid induction an additional hypersensitive site is detected approximately 2 kb upstream of the TAT promoter in liver and hepatoma cells.

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References

    1. J Biol Chem. 1967 Oct 10;242(19):4372-7 - PubMed
    1. Nat New Biol. 1972 Sep 6;239(88):9-14 - PubMed
    1. Science. 1976 Sep 3;193(4256):848-56 - PubMed
    1. Cancer Res. 1976 Oct;36(10):3594-9 - PubMed
    1. Cell. 1979 Feb;16(2):225-37 - PubMed

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