CpG island methylation and promoter usage in the parathyroid hormone- related protein gene of cultured lung cells
CpG island methylation and promoter usage in the parathyroid hormone- related protein gene of cultured lung cells
Excessive production of a parathyroid hormone-related protein (PTHrP) by turnouts commonly results in the syndrome of humoral hypercalcaemia of malignancy. We have investigated whether epigenetic changes play a role in over-expression of the PTHrP gene, using cultures lung cells as a model system. Study of the methylation status of CpG dinucleotides in the 5' region of the gene showed that in normal cells the CpG island was completely unmethylated. In the lung squamous cell carcinoma cell line, BEN, two-thirds of the CpG island was substantially methylated. RT-PCR analysis showed that this heavy methylation did not prevent expression of any of the three PTHrP gene promoters. This is a surprising finding, since methylation is usually associated with inhibition of gene activity. Methylation of the 5' non- coding region of the PTHrP gene may not play a role in the regulation of adjacent promoters. Alternatively, maintenance of a demethylated state in the 170 bp at the 3' end of the CpG island may be fundamental for the use of PTHrP promoters.
DNA methylation, Established cell line, Parathyroid hormone-related protein, Promoter usage
303-310
Ganderton, Rosalind H.
0cbaa3a4-8413-4a63-b48f-e582e14a2e35
Briggs, Roger S.J.
a6b65ef0-e90c-4c07-bf5b-b70130c128b3
26 June 1997
Ganderton, Rosalind H.
0cbaa3a4-8413-4a63-b48f-e582e14a2e35
Briggs, Roger S.J.
a6b65ef0-e90c-4c07-bf5b-b70130c128b3
Ganderton, Rosalind H. and Briggs, Roger S.J.
(1997)
CpG island methylation and promoter usage in the parathyroid hormone- related protein gene of cultured lung cells.
Biochimica et Biophysica Acta - Gene Structure and Expression, 1352 (3), .
(doi:10.1016/S0167-4781(97)00031-6).
Abstract
Excessive production of a parathyroid hormone-related protein (PTHrP) by turnouts commonly results in the syndrome of humoral hypercalcaemia of malignancy. We have investigated whether epigenetic changes play a role in over-expression of the PTHrP gene, using cultures lung cells as a model system. Study of the methylation status of CpG dinucleotides in the 5' region of the gene showed that in normal cells the CpG island was completely unmethylated. In the lung squamous cell carcinoma cell line, BEN, two-thirds of the CpG island was substantially methylated. RT-PCR analysis showed that this heavy methylation did not prevent expression of any of the three PTHrP gene promoters. This is a surprising finding, since methylation is usually associated with inhibition of gene activity. Methylation of the 5' non- coding region of the PTHrP gene may not play a role in the regulation of adjacent promoters. Alternatively, maintenance of a demethylated state in the 170 bp at the 3' end of the CpG island may be fundamental for the use of PTHrP promoters.
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Published date: 26 June 1997
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Funding Information:
We would like to thank the following for their help with these studies: Dr S.J. Cooke and Dr S.L. Zhang for provision of cultured cells, Professor R.J. Thompson for provision of laboratory space, Miss L.J. Hinks for invaluable technical advice and Mrs W. Keeling for typing of the manuscript. The BEN cell line was donated by Professor A. Munro-Neville from the Ludwig Institute for Cancer Research. The work was funded by the Cancer Research Campaign.
Keywords:
DNA methylation, Established cell line, Parathyroid hormone-related protein, Promoter usage
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Local EPrints ID: 479039
URI: http://eprints.soton.ac.uk/id/eprint/479039
ISSN: 0167-4781
PURE UUID: 8cf83d3f-7926-4695-b62f-d97b0cb576ee
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Date deposited: 19 Jul 2023 16:35
Last modified: 17 Mar 2024 13:24
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Author:
Rosalind H. Ganderton
Author:
Roger S.J. Briggs
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