Identification of genes periodically expressed in the human cell cycle and their expression in tumors. Author Michael Whitfield, Gavin Sherlock, Alok Saldanha, John Murray, Catherine Ball, Karen Alexander, John Matese, Charles Perou, Myra Hurt, Patrick Brown, David Botstein Publication Year 2002 Type Journal Article Abstract 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/. Keywords Gene Expression Regulation, Transcription, Genetic, Humans, Cell Cycle, Genetic Variation, Proteins, Multigene Family, Oligonucleotide Array Sequence Analysis, Genome, Human, Gene Expression Regulation, Neoplastic, Neoplasms, Mitosis, Cell Division, HeLa Cells, Enzymes, Transfection, DNA Replication Journal Mol Biol Cell Volume 13 Issue 6 Pages 1977-2000 Date Published 06/2002 Alternate Journal Mol. Biol. Cell Google ScholarBibTeXEndNote X3 XML