Correlation between gene functions and developmental expression patterns in the mouse cerebellum

被引:28
作者
Matoba, R
Kato, K [1 ]
Kurooka, C
Maruyama, C
Sakakibara, Y
Matsubara, K
机构
[1] Japan Sci & Technol Corp, CREST, Nara, Japan
[2] Nara Inst Sci & Technol, Taisho Lab Funct Genom, Nara 6300101, Japan
关键词
ATAC-PCR; cerebellum; cluster analysis; functional genomics;
D O I
10.1046/j.1460-9568.2000.01034.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Quantitative changes of 419 gene transcripts during postnatal mouse cerebellar development were accurately determined with a novel polymerase chain reaction (PCR)-based technique. About 70% of the genes showed differences in expression levels, and the magnitude of difference was relatively small. By hierarchic cluster analysis of developmental expression patterns, the genes were categorized into 19 clusters, which were subsequently assembled into four major groups: group 1, with elevation of gene expression throughout the time course; group 2, with relatively unchanged levels; group 3, with transiently high expression at similar to 12 days; and group 4, with highest expression at similar to 4 days. Genes related to brain functions were segregated into several clusters of group 1 and group 3: the same clusters in which cerebellum-specific genes were also segregated. Genes for protein synthesis belonged to group 4, Genes with housekeeping functions belonged to group 2. Western blotting analysis of representative protein products of each group revealed correlation with the mRNA level for those belonging to group 1 and group 4, but not necessarily in the other groups. The close correlation of algorithmically categorized temporal expression patterns of genes with their functions will be useful for estimating the functions of thousands of novel genes.
引用
收藏
页码:1357 / 1371
页数:15
相关论文
共 22 条
[2]  
[Anonymous], CLUSTANGRAPHICS PRIM
[3]   COMPLEXITY AND CHARACTERIZATION OF POLYADENYLATED RNA IN MOUSE-BRAIN [J].
BANTLE, JA ;
HAHN, WE .
CELL, 1976, 8 (01) :139-150
[4]   The transcriptional program of sporulation in budding yeast [J].
Chu, S ;
DeRisi, J ;
Eisen, M ;
Mulholland, J ;
Botstein, D ;
Brown, PO ;
Herskowitz, I .
SCIENCE, 1998, 282 (5389) :699-705
[5]   DEVELOPMENT OF MACROGLIAL CELLS IN RAT CEREBELLUM .1. USE OF ANTIBODIES TO FOLLOW EARLY INVIVO DEVELOPMENT AND MIGRATION OF OLIGODENDROCYTES [J].
CURTIS, R ;
COHEN, J ;
FOKSEANG, J ;
HANLEY, MR ;
GREGSON, NA ;
REYNOLDS, R ;
WILKIN, GP .
JOURNAL OF NEUROCYTOLOGY, 1988, 17 (01) :43-54
[6]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[7]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[8]   The cells and molecules that make a cerebellum [J].
Goldowitz, D ;
Hamre, K .
TRENDS IN NEUROSCIENCES, 1998, 21 (09) :375-382
[9]   IDENTIFICATION OF DIFFERENTIALLY EXPRESSED GENES BY RESTRICTION ENDONUCLEASE-BASED GENE-EXPRESSION FINGERPRINTING [J].
IVANOVA, NB ;
BELYAVSKY, AV .
NUCLEIC ACIDS RESEARCH, 1995, 23 (15) :2954-2958
[10]   SEQUENCE COMPLEXITY OF POLYADENYLATED RNA OBTAINED FROM RAT-BRAIN REGIONS AND CULTURED RAT CELLS OF NEURAL ORIGIN [J].
KAPLAN, BB ;
SCHACHTER, BS ;
OSTERBURG, HH ;
DEVELLIS, JS ;
FINCH, CE .
BIOCHEMISTRY, 1978, 17 (25) :5516-5524