An AscI boundary library for the studies of genetic and epigenetic alterations in CpG islands

被引:17
作者
Dai, ZY
Weichenhan, D
Wu, YZ
Hall, JL
Rush, LJ
Smith, LT
Raval, A
Yu, L
Kroll, D
Muehlisch, J
Frühwald, MC
de Jong, P
Catanese, J
Davuluri, RV
Smiraglia, DJ
Plass, C [1 ]
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Div Human Canc Genet, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Vet Biosci, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[5] Med Univ Lubeck, Med Klin 2, D-23538 Lubeck, Germany
[6] Univ Klinikum Munster, Klin & Poliklin Kinderheilkunde, D-48149 Munster, Germany
[7] Childrens Hosp, Oakland Res Inst, Oakland, CA 94609 USA
关键词
D O I
10.1101/gr.197402
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Nod as the restriction landmark site. Here, we describe the development of RLGS using Ascl as the restriction landmark site for genome-wide scans of cancer genomes. The availability of Ascl as a restriction landmark for RLGS allows for scanning almost twice as many CpG islands in the human genome compared with using Nod only. We describe the development of an Ascl-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 Ascl RLGS fragments via two methods by use of this library.
引用
收藏
页码:1591 / 1598
页数:8
相关论文
共 29 条
[1]   Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer [J].
Baylin, SB ;
Esteller, M ;
Rountree, MR ;
Bachman, KE ;
Schuebel, K ;
Herman, JG .
HUMAN MOLECULAR GENETICS, 2001, 10 (07) :687-692
[2]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[3]   Aberrant CpG-island methylation has non-random and tumour-type-specific patterns [J].
Costello, JF ;
Frühwald, MC ;
Smiraglia, DJ ;
Rush, LJ ;
Robertson, GP ;
Gao, X ;
Wright, FA ;
Feramisco, JD ;
Peltomäki, P ;
Lang, JC ;
Schuller, DE ;
Yu, L ;
Bloomfield, CD ;
Caligiuri, MA ;
Yates, A ;
Nishikawa, R ;
Huang, HJS ;
Petrelli, NJ ;
Zhang, XL ;
O'Dorisio, MS ;
Held, WA ;
Cavenee, WK ;
Plass, C .
NATURE GENETICS, 2000, 24 (02) :132-138
[4]  
Costello JF, 1997, CANCER RES, V57, P1250
[5]   Methylation matters [J].
Costello, JF ;
Plass, C .
JOURNAL OF MEDICAL GENETICS, 2001, 38 (05) :285-303
[6]   Global methylation profiling of lung cancer identifies novel methylated genes [J].
Dai, ZY ;
Lakshmanan, RR ;
Zhu, WG ;
Smiraglia, DJ ;
Rush, LJ ;
Frühwald, MC ;
Brena, RM ;
Li, B ;
Wright, FA ;
Ross, P ;
Otterson, GA ;
Plass, C .
NEOPLASIA, 2001, 3 (04) :314-323
[7]  
Frühwald MC, 2001, GENE CHROMOSOME CANC, V30, P38
[8]   Global and gene-specific methylation patterns in cancer:: Aspects of tumor biology and clinical potential [J].
Frühwald, MC ;
Plass, C .
MOLECULAR GENETICS AND METABOLISM, 2002, 75 (01) :1-16
[9]   Aberrant promoter methylation of previously unidentified target genes is a common abnormality in medulloblastomas -: Implications for tumor biology and potential clinical utility [J].
Frühwald, MC ;
O'Dorisio, MS ;
Dai, ZY ;
Tanner, SM ;
Balster, DA ;
Gao, X ;
Wright, FA ;
Plass, C .
ONCOGENE, 2001, 20 (36) :5033-5042
[10]   Gene amplification in PNETs/medulloblastomas:: mapping of a novel amplified gene within the MYCN amplicon [J].
Frühwald, MC ;
O'Dorisio, MS ;
Rush, LJ ;
Reiter, JL ;
Smiraglia, DJ ;
Wenger, G ;
Costello, JF ;
White, PS ;
Krahe, R ;
Brodeur, GM ;
Plass, C .
JOURNAL OF MEDICAL GENETICS, 2000, 37 (07) :501-509