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Quantitative proteomic analysis of human breast epithelial cells with differential telomere length.


ABSTRACT: Telomeres play important functional roles in cell proliferation, cell cycle regulation, and genetic stability, in which telomere length is critical. In this study, quantitative proteome comparisons for the human breast epithelial cells with short and long telomeres (184-hTERTL vs. 184-hTERTS and 90P-hTERTL vs. 90P-hTERTS), resulting from transfection of the human telomerase reverse transcriptase (hTERT) gene, were performed using cleavable isotope-coded affinity tags. More than 2000 proteins were quantified in each comparative experiment, with approximately 77% of the proteins identified in both analyses. In the cells with long telomeres, significant and consistent alterations were observed in metabolism (amino acid, nucleotide, and lipid metabolism), genetic information transmission (transcription and translation regulation, spliceosome and ribosome complexes), and cell signaling. Interestingly, the DNA excision repair pathway is enhanced, while integrin and its ligands are downregulated in the cells with long telomeres. These results may provide valuable information related to telomere functions.

SUBMITTER: Yu LR 

PROVIDER: S-EPMC2268026 | biostudies-literature | 2007 May

REPOSITORIES: biostudies-literature

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Quantitative proteomic analysis of human breast epithelial cells with differential telomere length.

Yu Li-Rong LR   Chan King C KC   Tahara Hidetoshi H   Lucas David A DA   Chatterjee Koushik K   Issaq Haleem J HJ   Veenstra Timothy D TD  

Biochemical and biophysical research communications 20070322 4


Telomeres play important functional roles in cell proliferation, cell cycle regulation, and genetic stability, in which telomere length is critical. In this study, quantitative proteome comparisons for the human breast epithelial cells with short and long telomeres (184-hTERTL vs. 184-hTERTS and 90P-hTERTL vs. 90P-hTERTS), resulting from transfection of the human telomerase reverse transcriptase (hTERT) gene, were performed using cleavable isotope-coded affinity tags. More than 2000 proteins wer  ...[more]

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