Molecular Biology of the Cell · 2002 · 400 citations · 98 references
Life SciencesMolecular BiologyOncologyCell CycleGene ExpressionMolecular OncologyCancer GenomicsCancer TranscriptomicsCell Cycle ControlCell Cycle Gene RegulationCell-cycle PhasesCell-cycle RegulationCancer Cell Line ModelsCell Cycle DynamicsCell Cycle Gene Expression OscillationsCell Cycle TranscriptomicsCell Cycle-dependent Gene ExpressionFunctional Marker DiscoveryGenome-wide Characterization
Cell cycle‑regulated transcripts of genes involved in fundamental processes such as DNA replication and chromosome segregation appear more highly expressed in proliferative tumors because they contain more cycling cells. The study aims to provide a comprehensive catalog of cell‑cycle regulated genes to serve as a starting point for functional discovery. The genome‑wide program of gene expression during the cell division cycle in a human cancer cell line (HeLa) was characterized using cDNA microarrays. More than 850 transcripts varied periodically, clustering into groups of known cell‑cycle genes and uncharacterized genes, and most genes linked to tumor proliferation were also periodic, though some were not. The full dataset is available at http://genome-www.stanford.edu/Human-CellCycle/HeLa/.
The genome-wide program of gene expression during the cell division cycle in a human cancer cell line (HeLa) was characterized using cDNA microarrays. Transcripts of >850 genes showed periodic variation during the cell cycle. Hierarchical clustering of the expression patterns revealed coexpressed groups of previously well-characterized genes involved in essential cell cycle processes such as DNA replication, chromosome segregation, and cell adhesion along with genes of uncharacterized function. Most of the genes whose expression had previously been reported to correlate with the proliferative state of tumors were found herein also to be periodically expressed during the HeLa cell cycle. However, some of the genes periodically expressed in the HeLa cell cycle do not have a consistent correlation with tumor proliferation. Cell cycle-regulated transcripts of genes involved in fundamental processes such as DNA replication and chromosome segregation seem to be more highly expressed in proliferative tumors simply because they contain more cycling cells. The data in this report provide a comprehensive catalog of cell cycle regulated genes that can serve as a starting point for functional discovery. The full dataset is available at http://genome-www.stanford.edu/Human-CellCycle/HeLa/ .
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