Vertebrate chromosomes terminate in variable numbers of T(2)AG(3) nucl
eotide repeats, In order to study telomere repeats at individual chrom
osomes, we developed novel, quantitative fluorescence in situ hybridiz
ation procedures using labeled (C(3)TA(2))(3) peptide nucleic acid and
digital imaging microscopy. Telomere fluorescence intensity values fr
om metaphase chromosomes of cultured human hematopoietic cells decreas
ed with the replication history of the cells, varied up to six-fold wi
thin a metaphase, and were similar between sister chromatid telomeres.
Surprisingly, telomere fluorescence intensity values within normal ad
ult bone marrow metaphases did not show a normal distribution, suggest
ing that a minimum number of repeats at each telomere is required and/
or maintained during normal hematopoiesis.