
doi: 10.1007/bf00173159
pmid: 8587124
Cyclin-dependent kinase inhibitors are a growing family of molecules that regulate important transitions in the cell cycle. At least one of these molecules, p16, has been implicated in human tumorigenesis while its close homolog, p15, is induced by cell contact and transforming growth factor-beta (TGF-beta). To investigate the evolutionary and functional features of p15 and p16, we have isolated mouse (Mus musculus) homologs of each gene. Comparative analysis of these sequences provides evidence that the genes have similar functions in mouse and human. In addition, the comparison suggests that a gene conversion event is part of the evolution of the human p15 and p16 genes.
Base Sequence, Tumor Suppressor Proteins, Molecular Sequence Data, Cell Cycle Proteins, Hominidae, Evolution, Molecular, Mice, Animals, Humans, Amino Acid Sequence, Enzyme Inhibitors, Carrier Proteins, Protein Kinase Inhibitors, Sequence Alignment, Sequence Analysis, Conserved Sequence, Cyclin-Dependent Kinase Inhibitor p16, Cyclin-Dependent Kinase Inhibitor p15
Base Sequence, Tumor Suppressor Proteins, Molecular Sequence Data, Cell Cycle Proteins, Hominidae, Evolution, Molecular, Mice, Animals, Humans, Amino Acid Sequence, Enzyme Inhibitors, Carrier Proteins, Protein Kinase Inhibitors, Sequence Alignment, Sequence Analysis, Conserved Sequence, Cyclin-Dependent Kinase Inhibitor p16, Cyclin-Dependent Kinase Inhibitor p15
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