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Dissociation of telomerase activity and telomere length maintenance in primitive human hematopoietic cells
Author(s) -
Jean Wang,
Jennifer K Warner,
Natalie Erdmann,
Peter M. Lansdorp,
Lea Harrington,
John E. Dick
Publication year - 2005
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0504161102
Subject(s) - telomere , telomerase , haematopoiesis , biology , ectopic expression , microbiology and biotechnology , telomerase reverse transcriptase , stem cell , telomerase rna component , senescence , cord blood , cell culture , cell division , cell , cancer research , genetics , dna , gene
Primitive human hematopoietic cells have low endogenous telomerase activity, yet telomeres are not maintained. In contrast, ectopic telomerase expression in fibroblasts and other cells leads to telomere length maintenance or elongation. It is unclear whether this disparity can be attributed to telomerase level or stems from fundamentally different telomere biology. Here, we show that telomerase overexpression does not prevent proliferation-associated telomere shortening in human hematopoietic cells, pointing to the existence of cell type-specific differences in telomere dynamics. Furthermore, we observed eventual stabilization of telomere length without detectable changes in telomerase activity during establishment of two leukemic cell lines from normal cord blood cells, indicating that additional cooperating events are required for telomere maintenance in immortalized human hematopoietic cells.

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