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Dramatic attenuation of hypusine formation on eukaryotic initiation factor 5A during senescence of IMR‐90 human diploid fibroblasts
Author(s) -
Chen Zong Ping,
Chen Kuang Yu
Publication year - 1997
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/(sici)1097-4652(199703)170:3<248::aid-jcp5>3.0.co;2-o
Subject(s) - biology , polyamine , biochemistry , eukaryotic initiation factor , senescence , spermidine , population , microbiology and biotechnology , enzyme , messenger rna , translation (biology) , gene , demography , sociology
Deoxyhypusine synthase catalyzes the conversion of lysine to deoxyhypusine residue on the eukaryotic initiation factor 5A (eIF‐5A) precursor using spermidine as the substrate. Subsequent hydroxylation of the deoxyhypusine residue completes hypusine formation on eIF‐5A. Hypusine formation is one of the most specific polyamine‐dependent biochemical events in eukaryotic cells. Although changes in polyamine metabolism have been demonstrated in human diploid fibroblasts during senescence (Chen and Chang, 1986, J. Cell. Physiol., 128:27–32.), it is unclear whether or not polyamine‐dependent hypusine formation itself is an age‐dependent biochemical event. In the present study, hypusine‐forming activity was measured by a radiolabeling assay in cells whose polyamines have been depleted by prior treatment of α‐difluoromethyl ornithine (DFMO). In addition, an in vitro cross‐labeling assay was developed for simultaneous measurement of the deoxyhypusine synthase activity and protein substrate (eIF‐5A precursor) amount. We showed that the hypusine‐forming activity in low‐passage presenescent IMR‐90 cells [population doubling level (PDL) = 15–23, termed young cells] was prominently induced by serum whereas little or no hypusine‐forming activity could be detected in late‐passage senescent cells (PDL = 46–54, termed old cells). The striking difference in hypusine‐forming activity between young and old cells was due to changes in both deoxyhypusine synthase activity and eIF‐5A precursor amount in IMR‐90 cells during senescence. However, Northern blot analysis showed no significant difference in the eIF‐5A messenger RNA (mRNA) between young and old cells, suggesting that the age‐dependent attenuation of eIF‐5A precursor protein may be regulated at either translational or posttranslational level. J. Cell. Physiol. 170:248–254, 1997. © 1997 Wiley‐Liss, Inc.