Detailed methylation analysis of CpG islands on human chromosome region 9p21
β Scribed by Robert J. Weeks; Ian M. Morison
- Book ID
- 102220585
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 395 KB
- Volume
- 45
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Deletion of 9p21 is the most commonly reported chromosomal abnormality in pediatric acute lymphoblastic leukemia, and published data suggest that the maternal chromosome is preferentially deleted. Preferential maternal deletion of 9p21 and reports of a differentially methylated region (DMR) and of parental effects in mice with lymphoma suggest there may be an unrecognized imprinted locus in this region. To screen for DMRs, we used the mcrBC/__Hpa__II screening method and peripheralβblood DNA. Of 36 CpG islands within an 8.5βMb region of 9p21, seven were identified as putative DMRs and were further analyzed by bisulfite sequencing. Neither any of the CpG islands nor a previously published putative DMR nearby showed evidence of differential parental methylation; however, the published DMR did demonstrate sequenceβdependent differential methylation. Our data, which showed heterogeneous and lowβlevel methylation of CpG islands, have obvious implications for methylation studies. This article contains Supplementary Material available at http://www.interscience.wiley.com/jpages/1045β2257/suppmat. Β© 2005 WileyβLiss, Inc.
π SIMILAR VOLUMES
We examined 149 lung cancer cell lines for homozygous deletions using 24 DNA markers, which were mapped and ordered in chromosome band 9p21, to define the target regions for 9p21 deletions in human lung cancer. Homozygous deletions were detected in 39 (26%) cell lines and clustered at 2 independent
The finger motif is a tandemly repeated DNA-binding domain recently identified in the primary structure of several eukaryotic transcriptional regulatory proteins. It has been proposed that some members of the finger-gene family are implicated in both normal cell proliferation and differentiation. We
Chromosome 9p has been reported to be a critical region of loss in various cancers. Our present study was designed to determine the frequency of deletions at different loci of chromosome 9p in microdissected samples of normal prostatic epithelium and carcinoma from the same patients. For this purpos