EVIDENCE FOR A PUTATIVE TELOMERASE REPRESSOR GENE IN THE 3P14.2-P21.1REGION

Telomeres, which are the repeated sequences located on both ends of ch romosomes in eukaryotes, are known to shorten with each cell division, and their eventual loss is thought to result in cellular senescence. Unlike normal somatic cells, most tumor cells show activation of telom erase, a ribonucleoprotein enzyme that stably maintains telomere lengt h by addition of the sequences of TTAGGG repeats to telomeres. The KC1 2 cell line derived from a renal cell carcinoma in a patient with von Hippel-Lindau disease showed telomerase activity and loss of heterozyg osity on the short arm of chromosome 3. Introduction of a normal human chromosome 3 into KC12 cells by microcell fusion induced cellular sen escence, accompanied by suppression of telomerase activity and shorten ing of telomere length. Microcell hybrids that escaped from cellular s enescence maintained telomere length and telomerase activity similar t o those of the parental KC12 cells. We previously showed a similar sup pression of telomerase activity by introduction of chromosome 3 into a nother renal cell carcinoma cell line, RCC23. The putative telomerase repressor gene was mapped to chromosome region 3p14.2-p21.1 by deletio n mapping of KC12 + chromosome 3 revertants that escaped from cellular senescence and by transfer of subchromosomal fragments of chromosome 3 into RCC23 cells. (C) 1998 Wiley-Liss, Inc.