Discovering altered genomic expression patterns in heart: transcriptome determination by serial analysis of gene expression

被引:12
作者
Anisimov, SV [1 ]
Lakatta, EG [1 ]
Boheler, KR [1 ]
机构
[1] NIA, Cardiovasc Sci Lab, NIH, Baltimore, MD 21224 USA
关键词
SAGE; heart failure; rodent; human; transcriptome;
D O I
10.1016/S1388-9842(01)00131-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The development of cardiovascular diseases such as heart failure involve functional changes that are beneficial short-term, but may be fatal long-term. Current therapeutic approaches are tailored to limit progression of a disease and to maintain quality of life. At a molecular level, these disease processes involve quantitative and qualitative changes in gene expression. Although some changes in mRNA abundance may not have direct protein correlates, analysis of all the mRNAs present in a cell population (the cells transcriptome) has become a focal point of genomic research. The aim is to provide information about the dynamics of total genome expression in response to environmental changes and point to candidate genes responsible for the cascade of events that result in a disease state. One way of performing these analyses utilizes the technique of Serial Analysis of Gene Expression (SAGE). This method evaluates thousands of expressed transcripts both quantitatively and qualitatively in a single assay. In the first of two reviews on transcriptome analysis, we describe the current state of genomic research for determination of the transcriptome by Serial Analysis of Gene Expression, present the first limited SAGE analysis of rodent heart gene expression, and discuss how results generated with this approach can be applied to the study and treatment of cardiovascular diseases. Published by Elsevier Science Ireland Ltd on behalf of European Society of Cardiology.
引用
收藏
页码:271 / 281
页数:11
相关论文
共 46 条
  • [1] The significance of digital gene expression profiles
    Audic, S
    Claverie, JM
    [J]. GENOME RESEARCH, 1997, 7 (10): : 986 - 995
  • [2] Targeted overexpression of the sarcoplasmic reticulum Ca2+-ATPase increases cardiac contractility in transgenic mouse hearts
    Baker, DL
    Hashimoto, K
    Grupp, IL
    Ji, Y
    Reed, T
    Loukianov, E
    Grupp, G
    Bhagwhat, A
    Hoit, B
    Walsh, R
    Marban, E
    Periasamy, M
    [J]. CIRCULATION RESEARCH, 1998, 83 (12) : 1205 - 1214
  • [3] BARTON PJR, 1995, MOL BIOL CARDIAC DEV
  • [4] High-throughput gene expression analysis using SAGE
    Bertelsen, AH
    Velculescu, VE
    [J]. DRUG DISCOVERY TODAY, 1998, 3 (04) : 152 - 159
  • [5] Molecular classification of cutaneous malignant melanoma by gene expression profiling
    Bittner, M
    Meitzer, P
    Chen, Y
    Jiang, Y
    Seftor, E
    Hendrix, M
    Radmacher, M
    Simon, R
    Yakhini, Z
    Ben-Dor, A
    Sampas, N
    Dougherty, E
    Wang, E
    Marincola, F
    Gooden, C
    Lueders, J
    Glatfelter, A
    Pollock, P
    Carpten, J
    Gillanders, E
    Leja, D
    Dietrich, K
    Beaudry, C
    Berens, M
    Alberts, D
    Sondak, V
    Hayward, N
    Trent, J
    [J]. NATURE, 2000, 406 (6795) : 536 - 540
  • [6] GENE-EXPRESSION IN CARDIAC-HYPERTROPHY
    BOHELER, KR
    SCHWARTZ, K
    [J]. TRENDS IN CARDIOVASCULAR MEDICINE, 1992, 2 (05) : 176 - 182
  • [7] Matrix gene expression and decompensated heart failure: The aged SHR model
    Boluyt, MO
    Bing, OHL
    [J]. CARDIOVASCULAR RESEARCH, 2000, 46 (02) : 239 - 249
  • [8] TRANSCRIPTIONAL REGULATION DURING CARDIAC GROWTH AND DEVELOPMENT
    CHIEN, KR
    ZHU, H
    KNOWLTON, KU
    MILLERHANCE, W
    VANBILSEN, M
    OBRIEN, TX
    EVANS, SM
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1993, 55 : 77 - 95
  • [9] Genes and physiology: Molecular physiology in genetically engineered animals
    Chien, KR
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) : 901 - 909
  • [10] REGULATION OF CARDIAC GENE-EXPRESSION DURING MYOCARDIAL GROWTH AND HYPERTROPHY - MOLECULAR STUDIES OF AN ADAPTIVE PHYSIOLOGICAL-RESPONSE
    CHIEN, KR
    KNOWLTON, KU
    ZHU, H
    CHIEN, S
    [J]. FASEB JOURNAL, 1991, 5 (15) : 3037 - 3046