Identification of differentially expressed genes in cardiac hypertrophy by analysis of expressed sequence tags

被引:100
作者
Hwang, DM
Dempsey, AA
Lee, CY
Liew, CC
机构
[1] Univ Toronto, Toronto Hosp, Dept Lab Med & Pathobiol, Ctr Cardiovasc Res,Cardiac Gene Unit, Toronto, ON M5G 1L5, Canada
[2] Chinese Univ Hong Kong, Dept Biochem, Shatin, Hong Kong, Peoples R China
关键词
D O I
10.1006/geno.2000.6171
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cardiac hypertrophy is an adaptive response to chronic hemodynamic overload. We employed a whole-genome approach using expressed sequence tags (ESTs) to characterize gene transcription and identify new genes overexpressed in cardiac hypertrophy. Analysis of general transcription patterns revealed a proportional increase in transcripts related to cell/organism defense and a decrease in transcripts related to cell structure and motility in hypertrophic hearts compared to normal hearts. Detailed comparison of individual gene expression identified 64 genes potentially overexpressed in hypertrophy, of 232 candidate genes derived from a set of 77,692 cardiac ESTs, including 47,856 ESTs generated in our laboratory. Of these, 29 were good candidates (P < 0.0002) and 35 were weaker candidates (P < 0.005). RT-PCR of a number of these candidate genes demonstrated correspondence of EST-based predictions of gene expression with irt vitro levels. Consistent with an organ under various stresses, up to one-half of the good candidates predicted to exhibit differential expression were genes potentially involved in stress response. Analyses of general transcription patterns and of single-gene expression levels were also suggestive of increased protein synthesis in the hypertrophic myocardium, Overall, these results depict a scenario compatible with current understanding of cardiac hypertrophy. However, the identification of several genes not previously known to exhibit increased expression in cardiac hypertrophy (e.g., prostaglandin D synthases; CD59 antigen) also suggests a number of new avenues for further investigation. These data demonstrate the utility of genome-based resources for investigating questions of cardiovascular biology and medicine. (C) 2000 Academic Press.
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页码:1 / 14
页数:14
相关论文
共 84 条
[1]   3,400 NEW EXPRESSED SEQUENCE TAGS IDENTIFY DIVERSITY OF TRANSCRIPTS IN HUMAN BRAIN [J].
ADAMS, MD ;
KERLAVAGE, AR ;
FIELDS, C ;
VENTER, JC .
NATURE GENETICS, 1993, 4 (03) :256-267
[2]   RAPID CDNA SEQUENCING (EXPRESSED SEQUENCE TAGS) FROM A DIRECTIONALLY CLONED HUMAN INFANT BRAIN CDNA LIBRARY [J].
ADAMS, MD ;
SOARES, MB ;
KERLAVAGE, AR ;
FIELDS, C ;
VENTER, JC .
NATURE GENETICS, 1993, 4 (04) :373-386
[3]   SEQUENCE IDENTIFICATION OF 2,375 HUMAN BRAIN GENES [J].
ADAMS, MD ;
DUBNICK, M ;
KERLAVAGE, AR ;
MORENO, R ;
KELLEY, JM ;
UTTERBACK, TR ;
NAGLE, JW ;
FIELDS, C ;
VENTER, JC .
NATURE, 1992, 355 (6361) :632-634
[4]  
ADAMS MD, 1995, NATURE, V377, P3
[5]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[6]   THE IDENTIFICATION OF NOVEL GENE-SEQUENCES OF THE HUMAN ADULT TESTIS [J].
AFFARA, NA ;
BENTLEY, E ;
DAVEY, P ;
PELMEAR, A ;
JONES, MH .
GENOMICS, 1994, 22 (01) :205-210
[7]   EXPRESSION AND CHROMOSOMAL LOCALIZATION OF CDNA CLONES FROM AN ENRICHED HUMAN RETINAL-PIGMENT EPITHELIAL (RPE) CELL-LINE LIBRARY - IDENTIFICATION OF 2 RPE-SPECIFIC GENES [J].
AGARWAL, N ;
SWAROOP, A ;
ZHENG, K ;
LIOU, JD ;
OROURKE, K ;
GRAVES, KA ;
GIESER, L ;
DELMONTE, M ;
YANGFENG, TL .
CYTOGENETICS AND CELL GENETICS, 1995, 69 (1-2) :71-74
[8]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P410
[9]   Secretion of cardiac plasminogen activator during hypoxia-induced right ventricular hypertrophy [J].
Bansal, DD ;
Klein, RM ;
Hausmann, EHS ;
MacGregor, RR .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (11) :3105-3114
[10]   Analysis of a sequenced cDNA library from multiple sclerosis lesions [J].
Becker, KG ;
Mattson, DH ;
Powers, JM ;
Gado, AM ;
Biddison, WE .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 77 (01) :27-38