Telomeres are repeated DNA sequences, positioned at the ends of chromosomes
and are essential for the stable maintenance of chromosomes. The telomere
length serves as a mitotic clock determining the remaining replicative capa
city of the cell. Telomeric sequences are lost during each cell division, l
eading to a process thought to contribute to senescence and cell death. The
enzyme telomerase adds 5'-TTAGGG-3' repeats to the mammalian telomeres and
maintains the telomere length. Telomerase is normally inactive in most som
atic cells but telomerase activity is observed in malignancies. In this stu
dy telomerase activity was analyzed in patients with chronic myeloid leukem
ia (CML) and lymphoma by PCR and ELISA. This approach combines highly speci
fic amplification of the telomerase-mediated elongation products with nonra
dioactive detection in a highly sensitive photometric ELISA. The PCR produc
ts were also analyzed by Southern blotting. The telomerase-specific PCR pro
ducts were seperated by electrophoresis and transferred to a nylon membrane
with subsequent detection of the biotinylated amplificates. High activity
levers were detected in 17 CML ( 34 %) patients. On the other hand, no acti
vity was observed in lymphoma patients. An increase in the shorter telomeri
c bands was observed in CML patients who displayed a high level of telomera
se activity. In contrast to the low enzyme activity, evidence of telomeric
repeats were also found in some lymphoma patients by Southern blotting. Thi
s may indicate that lymphoma cells may make use of different pathways for m
aintaining the length of their telomeres.