The University of Southampton
University of Southampton Institutional Repository

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
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
0167-4781
303-310
Ganderton, Rosalind H.
0cbaa3a4-8413-4a63-b48f-e582e14a2e35
Briggs, Roger S.J.
a6b65ef0-e90c-4c07-bf5b-b70130c128b3
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), 303-310. (doi:10.1016/S0167-4781(97)00031-6).

Record type: Article

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.

This record has no associated files available for download.

More information

Published date: 26 June 1997
Additional Information: 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

Identifiers

Local EPrints ID: 479039
URI: http://eprints.soton.ac.uk/id/eprint/479039
ISSN: 0167-4781
PURE UUID: 8cf83d3f-7926-4695-b62f-d97b0cb576ee

Catalogue record

Date deposited: 19 Jul 2023 16:35
Last modified: 17 Mar 2024 13:24

Export record

Altmetrics

Contributors

Author: Rosalind H. Ganderton
Author: Roger S.J. Briggs

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×