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PMID: 8463324 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Molecular cloning of the cDNAs for the four subunits of mouse DNA polymerase alpha-primase complex and their gene expression during cell proliferation and the cell cycle.

The Journal of biological chemistry ·Vol. 268 ·No. 11 ·1993-04-15 ·Pages 8111-22

Miyazawa H, Izumi M, Tada S, Takada R, Masutani M, Ui M, Hanaoka F

Abstract

The DNA polymerase alpha-primase complex purified from mouse FM3A cells is composed of four polypeptides with molecular masses of 180, 68, 54, and 46 kDa. The largest subunit has DNA polymerase activity, the two smallest subunits have DNA primase activity, and the function of the 68-kDa subunit is unknown. We have isolated the cDNAs of the four subunits by low stringency hybridization and reverse transcription polymerase chain reaction and determined their nucleotide sequences. The predicted amino acid sequence of the 180-kDa subunit shows 88, 38, 34, and 32% identity to those of the catalytic subunits of human, Drosophila melanogaster, Schizosaccharomyces pombe, and Saccharomyces cerevisiae DNA polymerase alpha, respectively, and contains seven regions whose orders and sequences are highly conserved among viral and other eukaryotic DNA polymerases. The deduced amino acid sequence of the 68-kDa subunit shows 25% identity to that of the 73-kDa subunit of D. melanogaster DNA polymerase alpha-primase, shows no significant sequence similarity to any other protein in the data bases, but contains a potential phosphorylation site(s) for cdc2 kinase. The amino acid sequence of the 54-kDa subunit shows 32% identity to that of the large subunit of S. cerevisiae DNA primase. During activation of quiescent Swiss mouse 3T3 cells to proliferate, the levels of mRNA of the four subunits of the DNA polymerase alpha-primase complex increased before DNA synthesis. In growing mouse FM3A cells, the transcripts of the four subunits are present throughout the cell cycle and increase slightly prior to the S phase.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Cycle/physiology Cell Division/physiology Cloning, Molecular/methods DNA/genetics,metabolism DNA Polymerase II/genetics DNA Primase Drosophila melanogaster/enzymology,genetics Gene Library Macromolecular Substances Mammary Neoplasms, Experimental Mice Molecular Sequence Data Molecular Weight RNA Nucleotidyltransferases/genetics,metabolism RNA, Messenger/metabolism Restriction Mapping Saccharomyces cerevisiae/enzymology,genetics Schizosaccharomyces/enzymology,genetics Sequence Homology, Amino Acid Tumor Cells, Cultured
Chemicals
Macromolecular Substances RNA, Messenger DNA DNA Primase RNA Nucleotidyltransferases DNA Polymerase II
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Miyazawa H
Cellular Physiology Laboratory, Institute of Physical and Chemical Research (RIKEN), Wako, Saitama, Japan.
Izumi M
Tada S
Takada R
Masutani M
Ui M
Hanaoka F
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1993-04-15
Pages
8111-22
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
D13543, D13544, D13545, D13546
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