Identification of calcium- and nitric oxide-regulated genes by differential analysis of library expression (DAzLE)

被引:22
作者
Li, HW
Gu, XJ
Dawson, VL
Dawson, TM
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Inst Cell Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Physiol, Baltimore, MD 21205 USA
关键词
D O I
10.1073/pnas.0305145101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Using a method of expression profiling called differential analysis of cDNA library expression (DAzLE), we report the expression profile of late response genes in a model of activity-dependent neuronal survival and neurite outgrowth. Using DAzLE, we isolated differentially expressed genes from cultured rat embryonic cortical neurons after KCl (50 mM)-mediated membrane depolarization. We identified 469 activity-dependent regulated genes, of which 174 are genes of unknown function. The regulation of 63 genes was found to be nitric oxide (NO)-dependent. Identifiable genes fell into several major categories, including signal transduction pathways, neuronal development, DNA replication, gene transcription, protein metabolism, energy regulatory proteins, and antiapoptotic proteins. These genes may be important in activity-dependent neuron survival and development. Furthermore, these late response genes provide the tools to begin to investigate downstream events in activity-dependent neuronal survival and development. The major advantage of DAzLE is that it provides a nearly complete and relatively comprehensive differential screening profile that has the potential to be a powerful and useful tool in other fields of study.
引用
收藏
页码:647 / 652
页数:6
相关论文
共 45 条
[11]   RDA of lymphocyte subsets [J].
Frazer, JK ;
Pascual, V ;
Capra, JD .
JOURNAL OF IMMUNOLOGICAL METHODS, 1997, 207 (01) :1-12
[12]   REQUIREMENT FOR BDNF IN ACTIVITY-DEPENDENT SURVIVAL OF CORTICAL-NEURONS [J].
GHOSH, A ;
CARNAHAN, J ;
GREENBERG, ME .
SCIENCE, 1994, 263 (5153) :1618-1623
[13]   Extracellular-signal-regulated kinase signalling in neurons [J].
Grewal, SS ;
York, RD ;
Stork, PJS .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (05) :544-553
[14]   Hippocampal plasticity involves extensive gene induction and multiple cellular mechanisms [J].
Hevroni, D ;
Rattner, A ;
Bundman, M ;
Lederfein, D ;
Gabarah, A ;
Mangelus, M ;
Silverman, MA ;
Kedar, H ;
Naor, C ;
Kornuc, M ;
Hanoch, T ;
Seger, R ;
Theill, LE ;
Nedivi, E ;
Richter-Levin, G ;
Citri, Y .
JOURNAL OF MOLECULAR NEUROSCIENCE, 1998, 10 (02) :75-98
[15]  
HONG SJ, 2003, IN PRESS P NATL ACAD
[16]   IDENTIFYING DIFFERENCES IN MESSENGER-RNA EXPRESSION BY REPRESENTATIONAL DIFFERENCE ANALYSIS OF CDNA [J].
HUBANK, M ;
SCHATZ, DG .
NUCLEIC ACIDS RESEARCH, 1994, 22 (25) :5640-5648
[17]   Use of RDA analysis of knockout mice to identify myeloid genes regulated in vivo by PU.1 and C/EBPα [J].
Iwama, A ;
Zhang, P ;
Darlington, GJ ;
McKercher, SR ;
Maki, R ;
Tenen, DG .
NUCLEIC ACIDS RESEARCH, 1998, 26 (12) :3034-3043
[18]   A literature network of human genes for high-throughput analysis of gene expression [J].
Jenssen, TK ;
Lægreid, A ;
Komorowski, J ;
Hovig, E .
NATURE GENETICS, 2001, 28 (01) :21-+
[19]   RaSH, a rapid subtraction hybridization approach for identifying and cloning differentially expressed genes [J].
Jiang, HP ;
Kang, DC ;
Alexandre, D ;
Fisher, PB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12684-12689
[20]  
Jiang HP, 1995, ONCOGENE, V11, P2477