Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA

نویسندگان

  • María A Blasco
  • Han-Woong Lee
  • M.Prakash Hande
  • Enrique Samper
  • Peter M Lansdorp
  • Ronald A DePinho
  • Carol W Greider
چکیده

To examine the role of telomerase in normal and neoplastic growth, the telomerase RNA component (mTR) was deleted from the mouse germline. mTR-/- mice lacked detectable telomerase activity yet were viable for the six generations analyzed. Telomerase-deficient cells could be immortalized in culture, transformed by viral oncogenes, and generated tumors in nude mice following transformation. Telomeres were shown to shorten at a rate of 4.8+/-2.4 kb per mTR-/- generation. Cells from the fourth mTR-/- generation onward possessed chromosome ends lacking detectable telomere repeats, aneuploidy, and chromosomal abnormalities, including end-to-end fusions. These results indicate that telomerase is essential for telomere length maintenance but is not required for establishment of cell lines, oncogenic transformation, or tumor formation in mice.

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عنوان ژورنال:
  • Cell

دوره 91  شماره 

صفحات  -

تاریخ انتشار 1997