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POLN, a nuclear PolA family DNA polymerase homologous to the DNA cross-link sensitivity protein Mus308.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2003 Aug 22; Vol. 278 (34), pp. 32014-9. Date of Electronic Publication: 2003 Jun 06. - Publication Year :
- 2003
-
Abstract
- The Drosophila Mus308 gene is unusual in encoding both a family A DNA polymerase domain and a DNA/RNA helicase domain. A mus308 mutation was shown to result in increased sensitivity to DNA cross-linking agents, leading to the hypothesis that Mus308 functions in the repair of DNA interstrand cross-links. Recently a mammalian ortholog of Mus308, POLQ, has been identified. We report here the identification, cloning, and characterization of POLN and its gene product, a new mammalian DNA polymerase also related to Mus308. The human cDNA encodes a protein of 900 amino acid residues. The region starting from residue 419 shares 33% identity (48% similarity) with the equivalent region of Escherichia coli DNA polymerase I. POLN is expressed in human cell lines with numerous alternatively spliced transcripts, and a full-length human coding region that comprises 24 exons within 160 kilobases of genomic DNA. Expression analysis by northern blotting and in situ hybridization showed highest expression of full-length POLN in human and mouse testis. POLN localized to the nucleus when expressed as a enhanced green fluorescent protein (GFP)-tagged protein in human fibroblasts. GFP-tagged recombinant POLN had DNA polymerase activity on activated calf thymus DNA and on a singly primed template.
- Subjects :
- Amino Acid Sequence
Animals
Base Sequence
Chromosome Mapping
DNA Polymerase I chemistry
DNA Polymerase I genetics
DNA Primers
DNA Repair Enzymes
DNA-Directed DNA Polymerase
Humans
Male
Mice
Molecular Sequence Data
Sequence Homology, Amino Acid
Testis enzymology
DNA metabolism
DNA Polymerase I metabolism
Drosophila Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 278
- Issue :
- 34
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12794064
- Full Text :
- https://doi.org/10.1074/jbc.M305646200