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J. Biol. Chem., Vol. 269, Issue 39, 24027-24033, 09, 1994
XR Zeng, H Hao, Y Jiang and MY Lee
The expression of polymerase delta (pol delta) during the cell cycle was
studied in Molt 4 cells separated by counter-flow centrifugal elutriation.
Northern blotting showed that pol delta mRNA levels increased by 3-fold at
the G1/S border. Levels of pol delta protein determined by Western blotting
also peaked at the G1/S border with qualitatively similar changes as the
mRNA levels. Thus, pol delta gene expression appears to be regulated during
the cell cycle at the transcriptional level. The mRNA half-life for pol
delta was determined to be about 8 h and the protein half-life about 10 h.
Parallel examination of the expression of proliferating cell nuclear
antigen showed that the mRNA levels also increased about 2-fold at the G1/S
border, while the protein levels of proliferating cell nuclear antigen
increased steadily through the whole cell cycle period, and remained high
at G2/M. Analysis of pol alpha expression showed qualitatively similar
behavior as pol delta, but the magnitude of the changes were higher. Pulse
labeling of cells metabolically arrested in G1,S, or G2/M with 32Pi showed
that pol delta is a phosphoprotein and that it is most actively
phosphorylated during the S phase.
Regulation of human DNA polymerase delta during the cell cycle
Department of Medicine, University of Miami School of Medicine, Florida 33101.
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