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An AscI Boundary Library for the Studies of Genetic and Epigenetic Alterations in CpG Islands
Author(s) -
Zunyan Dai,
Dieter Weichenhan,
Yue-Zhong Wu,
Julia Hall,
Laura J. Rush,
Laura T. Smith,
Aparna Raval,
Li Yu,
Daniela Kroll,
J Muehlisch,
Michael C. Frühwald,
Peter J. de Jong,
Joe Catanese,
Ramana V. Davuluri,
Dominic J. Smiraglia,
Christoph Plass
Publication year - 2002
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.197402
Subject(s) - biology , genetics , dna methylation , epigenetics , genome , cpg site , gene , positional cloning , computational biology , locus (genetics) , gene expression
Knudson's two-hit hypothesis postulates that genetic alterations in both alleles are required for the inactivation of tumor-suppressor genes. Genetic alterations include small or large deletions and mutations. Over the past years, it has become clear that epigenetic alterations such as DNA methylation are additional mechanisms for gene silencing. Restriction Landmark Genomic Scanning (RLGS) is a two-dimensional gel electrophoresis that assesses the methylation status of thousands of CpG islands. RLGS has been applied successfully to scan cancer genomes for aberrant DNA methylation patterns. So far, the majority of this work was done using NotI as the restriction landmark site. Here, we describe the development of RLGS using AscI as the restriction landmark site for genome-wide scans of cancer genomes. The availability of AscI as a restriction landmark for RLGS allows for scanning almost twice as many CpG islands in the human genome compared with using NotI only. We describe the development of an AscI-EcoRV boundary library that supports the cloning of novel methylated genes. Feasibility of this system is shown in three tumor types, medulloblastomas, lung cancers, and head and neck cancers. We report the cloning of 178 AscI RLGS fragments via two methods by use of this library.

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