Characterization of the 5′-flanking region of the gene encoding the 50 kDa subunit of human DNA polymerase δ

Abstract

DNA polymerase δ consists of at least four subunits: p125, p68, p50, and p12 [Liu et al., J. Biol. Chem. 275 (2000) 18739–18744]. We have isolated genomic DNA clones covering the gene for the human DNA polymerase δ 50 kDa subunit (POLD2) and its 5′-flanking sequence. The POLD2 gene is composed of 11 exons and is distributed over 10 kb of genomic DNA. All exon–intron splice junctions conformed to the GT/AG consensus sequence. The 5′-flanking region of human POLD2 is G+C-rich and does not have a typical TATA box. A computer-based search for potential transcription factor binding sites revealed the existence of a number of motifs including those for AP1, AP2, Sp1, NF-1 and CREB. The functional activity of the regulatory region of the human POLD2 gene was demonstrated by its ability to drive the expression of a chloramphenicol acetyltransferase reporter gene in COS-7 cells.