Genome-scale approaches to the epigenetics of common human disease

被引:100
作者
Feinberg, Andrew P. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Ctr Epigenet, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
关键词
Epigenetics; Epidemiology; DNA methylation; BECKWITH-WIEDEMANN-SYNDROME; MODERATE FOLATE-DEPLETION; AGE-RELATED REACTIVATION; IN-VITRO FERTILIZATION; DNA METHYLATION; CPG ISLANDS; CYTOSINE METHYLATION; P53; GENE; CANCER; HYPOMETHYLATION;
D O I
10.1007/s00428-009-0847-2
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Traditionally, the pathology of human disease has been focused on microscopic examination of affected tissues, chemical and biochemical analysis of biopsy samples, other available samples of convenience, such as blood, and noninvasive or invasive imaging of varying complexity, in order to classify disease and illuminate its mechanistic basis. The molecular age has complemented this armamentarium with gene expression arrays and selective analysis of individual genes. However, we are entering a new era of epigenomic profiling, i.e., genome-scale analysis of cell-heritable nonsequence genetic change, such as DNA methylation. The epigenome offers access to stable measurements of cellular state and to biobanked material for large-scale epidemiological studies. Some of these genome-scale technologies are beginning to be applied to create the new field of epigenetic epidemiology.
引用
收藏
页码:13 / 21
页数:9
相关论文
共 83 条
[1]   Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene [J].
Alarcon, Maricela ;
Abrahams, Brett S. ;
Stone, Jennifer L. ;
Duvall, Jacqueline A. ;
Perederiy, Julia V. ;
Bomar, Jamee M. ;
Sebat, Jonathan ;
Wigler, Michael ;
Martin, Christa L. ;
Ledbetter, David H. ;
Nelson, Stanley E. ;
Cantor, Rita M. ;
Geschwind, Daniel H. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) :150-159
[2]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[3]   A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism [J].
Arking, Dan E. ;
Cutler, David J. ;
Brune, Camille W. ;
Teslovich, Tanya M. ;
West, Kristen ;
Ikeda, Morna ;
Rea, Alexis ;
Guy, Moltu ;
Lin, Shin ;
Cook, Edwin H., Jr. ;
Chakravarti, Aravinda .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) :160-164
[4]   Molecular cytogenetic analysis and resequencing of Contactin Associated Protein-Like 2 in autism spectrum disorders [J].
Bakkaloglu, Betul ;
O'Roak, Brian J. ;
Louvi, Angeliki ;
Gupta, Abha R. ;
Abelson, Jesse E. ;
Morgan, Thomas M. ;
Chawarska, Katarzyna ;
Klin, Ami ;
Ercan-Sencicek, A. Gulhan ;
Stillman, Althea A. ;
Tanriover, Gamze ;
Abrahams, Brett S. ;
Duvall, Jackie A. ;
Robbins, Elissa M. ;
Geschwind, Daniel H. ;
Biederer, Thomas ;
Gunel, Murat ;
Lifton, Richard P. ;
State, Matthew W. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) :165-173
[5]   Phenotype of frailty: Characterization in the women's health and aging studies [J].
Bandeen-Roche, K ;
Xue, QL ;
Ferrucci, L ;
Walston, J ;
Guralnik, JM ;
Chaves, P ;
Zeger, SL ;
Fried, LP .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2006, 61 (03) :262-266
[6]  
Bennett-Baker PE, 2003, GENETICS, V165, P2055
[7]   The DNA methyltransferases of mammals [J].
Bestor, TH .
HUMAN MOLECULAR GENETICS, 2000, 9 (16) :2395-2402
[8]   High-throughput DNA methylation profiling using universal bead arrays [J].
Bibikova, M ;
Lin, ZW ;
Zhou, LX ;
Chudin, E ;
Garcia, EW ;
Wu, B ;
Doucet, D ;
Thomas, NJ ;
Wang, YH ;
Vollmer, E ;
Goldmann, T ;
Seifart, C ;
Jiang, W ;
Barker, DL ;
Chee, MS ;
Floros, J ;
Fan, JB .
GENOME RESEARCH, 2006, 16 (03) :383-393
[9]  
Bibikova Marina, 2009, V507, P149, DOI 10.1007/978-1-59745-522-0_12
[10]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213