Implication of abnormal epigenetic patterns for human diseases

被引:78
作者
Santos-Reboucas, C. B. [1 ]
Pimentel, M. M. G. [1 ]
机构
[1] Univ Estado Rio De Janeiro, Dept Biol Celular & Genet, Serv Genet Humana, Inst Biol Roberto Alcantara Gomes, BR-20550013 Rio De Janeiro, Brazil
关键词
epigenetic diseases; epigenome; DNA methylation; imprinting; chromatin remodeling; PcG proteins;
D O I
10.1038/sj.ejhg.5201727
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
Significant evidences have brought new insights on the mechanisms by which epigenetic machinery proteins regulate gene expression, leading to a redefinition of chromatin regulation in terms of modification of core histones, DNA methylation, RNA-mediated silencing pathways, action of methylation-dependent sensitive insulators and Polycomb/Trithorax group proteins. Consistent with these fundamental aspects, an increasing number of human pathologies have been found to be associated with aberrant epigenetics regulation, including cancer, mental retardation, neurodegenerative symptoms, imprinting disorders, syndromes involving chromosomal instabilities and a great number of human life-threatening diseases. The possibility of reversing epigenetic marks, in contrast to genetic code, may provide new pharmacological targets for emerging therapeutic intervention.
引用
收藏
页码:10 / 17
页数:8
相关论文
共 95 条
[21]   Homocysteine and stroke [J].
Hankey, GJ ;
Eikelboom, JW .
CURRENT OPINION IN NEUROLOGY, 2001, 14 (01) :95-102
[22]   Maternal folate polymorphisms and the etiology of human nondisjunction [J].
Hassold, TJ ;
Burrage, LC ;
Chan, ER ;
Judis, LM ;
Schwartz, S ;
James, SJ ;
Jacobs, PA ;
Thomas, NS .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (02) :434-439
[23]   Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation [J].
Heard, E ;
Rougeulle, C ;
Arnaud, D ;
Avner, P ;
Allis, CD ;
Spector, DL .
CELL, 2001, 107 (06) :727-738
[24]   Folate levels in psychiatric outpatients [J].
Herrán, A ;
García-Unzueta, MT ;
Amado, JA ;
López-Cordovilla, JJ ;
Díez-Manrique, JF ;
Vázquez-Barquero, JL .
PSYCHIATRY AND CLINICAL NEUROSCIENCES, 1999, 53 (04) :531-533
[25]   Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease [J].
Hockly, E ;
Richon, VM ;
Woodman, B ;
Smith, DL ;
Zhou, XB ;
Rosa, E ;
Sathasivam, K ;
Ghazi-Noori, S ;
Mahal, A ;
Lowden, PAS ;
Steffan, JS ;
Marsh, JL ;
Thompson, LM ;
Lewis, CM ;
Marks, PA ;
Bates, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (04) :2041-2046
[26]   HIGH-RESOLUTION METHYLATION ANALYSIS OF THE HUMAN HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE GENE 5' REGION ON THE ACTIVE AND INACTIVE X-CHROMOSOMES - CORRELATION WITH BINDING-SITES FOR TRANSCRIPTION FACTORS [J].
HORNSTRA, IK ;
YANG, TP .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (02) :1419-1430
[27]  
Huang Luyun, 2003, P175
[28]  
Issa JP, 2000, CURR TOP MICROBIOL, V249, P101
[29]   Phase 1 study of low-dose prolonged exposure schedules of the hypomethylating agent 5-aza-2′-deoxycytidine (decitabine) in hematopoietic malignancies [J].
Issa, JPJ ;
Garcia-Manero, G ;
Giles, FJ ;
Mannari, R ;
Thomas, D ;
Faderl, S ;
Bayar, E ;
Lyons, J ;
Rosenfeld, CS ;
Cortes, J ;
Kantarjian, HM .
BLOOD, 2004, 103 (05) :1635-1640
[30]   X-linked Coffin-Lowry syndrome (CLS, MIM 303600, RPS6KA3 gene, protein product known under various names:: pp90rsk2, RSK2, ISM, MAPKAP1) [J].
Jacquot, S ;
Zeniou, M ;
Touraine, R ;
Hanauer, A .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 (01) :2-5