Gene expression profiling of HeLa cells in G1 or G2 phases

被引:25
作者
Chaudhry, MA
Chodosh, LA
McKenna, WG
Muschel, RJ
机构
[1] Univ Penn, Sch Med, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Canc Biol, Abramson Canc Res Inst, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
microarray; genechip; cell cycle;
D O I
10.1038/sj.onc.1205264
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
The cell division cycle is regulated through both transcriptional and post-transcriptional mechanisms. The altered expression of a number of genes at the mRNA level is known to be essential for progression through the cell cycle, however, a comprehensive gene expression profile of human cells remains to be completed. Here we sought to monitor the differential gene expression of genes after the transition of G2 cells into G1 prior to the restriction point. GeneChip containing microarrays of oligonucleotides corresponding to over 12 000 human genes were employed to profile differential gene expression in G1 and G2. After three independent experiments the resultant data was filtered and a set of genes was compiled based on at least threefold-altered expression, no background noise in determining expression and observation in all experiments. Our analysis identified 154 genes that were elevated in G2 phase of cells as compared to early G1 phase including 15 novel genes. This number included mRNAs whose upregulation is known to occur in G2 phase. Surprisingly only 19 genes were upregulated in G1 phase, among these six genes were novel. Some of these genes are candidates for transition through early G1. This gene inventory for G1 and G2 phases of cell cycle will provide the basis for understanding of cell cycle delay as a result of DNA damage.
引用
收藏
页码:1934 / 1942
页数:9
相关论文
共 30 条
[1]  
ALBERTS B, 1994, MOL BIOL CELL, P369
[2]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[3]   Transcriptional regulation and function during the human cell cycle [J].
Cho, RJ ;
Huang, MX ;
Campbell, MJ ;
Dong, HL ;
Steinmetz, L ;
Sapinoso, L ;
Hampton, G ;
Elledge, SJ ;
Davis, RW ;
Lockhart, DJ .
NATURE GENETICS, 2001, 27 (01) :48-54
[4]   Gene number - What if there are only 30,000 human genes? [J].
Claverie, JM .
SCIENCE, 2001, 291 (5507) :1255-1257
[5]   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
[6]   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
[7]   Cdc2-independent induction of premature mitosis by okadaic acid in HeLa cells [J].
Ghosh, S ;
Paweletz, N ;
Schroeter, D .
EXPERIMENTAL CELL RESEARCH, 1998, 242 (01) :1-9
[8]   CELL-DEATH AND THE CELL-CYCLE - A RELATIONSHIP BETWEEN TRANSFORMATION AND NEURODEGENERATION [J].
HEINTZ, N .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (05) :157-159
[9]   Ras-dependent cell cycle commitment during G2 phase [J].
Hitomi, M ;
Stacey, DW .
FEBS LETTERS, 2001, 490 (03) :123-131
[10]  
KATO J, 1999, FRONT BIOSCI, V1, P787