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The Chromatin Structure at the Promoter of a Glyceraldehyde Phosphate Dehydrogenase Gene from Saccharomyces Cerevisiae Reflects Its Functional State

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Journal Mol Cell Biol
Specialty Cell Biology
Date 1988 Dec 1
PMID 2854200
Citations 22
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Abstract

The chromatin structure of TDH3, one of three genes encoding glyceraldehyde phosphate dehydrogenases in Saccharomyces cerevisiae, was analyzed by nuclease digestion. A large hypersensitive region was found at the TDH3 promoter extending from the RNA initiation site at position -40 to position -560. This hypersensitive domain is nucleosome free and includes all putative cis-acting regulatory DNA elements. It is equally present in cells grown on fermentable as well as nonfermentable carbon sources. In a mutant which lacks the trans-activating protein GCR1 and which as a consequence expresses TDH3 at less than 5% of the wild-type level, the chromatin structure is different. Hypersensitivity between -40 and -370 is lost, due to the deposition of nucleosomes on a stretch that is nucleosome free in wild-type cells. Hypersensitivity is retained, however, further upstream (from -370 to -560). A similarly altered chromatin structure, as in a ger1 mutant, is found in wild-type cells when they approach stationary phase. This is the first evidence for a growth-dependent regulation of the TDH3 promoter.

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References
1.
Wintersberger U, Smith P, Letnansky K . Yeast chromatin. Preparation from isolated nuclei, histone composition and transcription capacity. Eur J Biochem. 1973; 33(1):123-30. DOI: 10.1111/j.1432-1033.1973.tb02663.x. View

2.
Matsumoto K, Uno I, Ishikawa T . Genetic analysis of the role of cAMP in yeast. Yeast. 1985; 1(1):15-24. DOI: 10.1002/yea.320010103. View

3.
Holland M, Holland J . Isolation and characterization of a gene coding for glyceraldehyde-3-phosphate dehydrogenase from Saccharomyces cerevisiae. J Biol Chem. 1979; 254(12):5466-74. View

4.
Holland J, Holland M . The primary structure of a glyceraldehyde-3-phosphate dehydrogenase gene from Saccharomyces cerevisiae. J Biol Chem. 1979; 254(19):9839-45. View

5.
Nedospasov S, Georgiev G . Non-random cleavage of SV40 DNA in the compact minichromosome and free in solution by micrococcal nuclease. Biochem Biophys Res Commun. 1980; 92(2):532-9. DOI: 10.1016/0006-291x(80)90366-6. View