Structure of human phenylethanolamine n-methyltransferase gene: existence of two types of mRNA with different transcription initiation sites

T Sasaoka; N Kaneda; Y Kurosawa; K Fujita; T Nagatsu

doi:10.1016/0197-0186(89)90176-9

Structure of human phenylethanolamine n-methyltransferase gene: existence of two types of mRNA with different transcription initiation sites

Neurochem Int. 1989;15(4):555-65. doi: 10.1016/0197-0186(89)90176-9.

Authors

T Sasaoka¹, N Kaneda, Y Kurosawa, K Fujita, T Nagatsu

Affiliation

¹ Department of Biochemistry, Nagoya University School of Medicine, Nagoya 466, Japan.

PMID: 20504532
DOI: 10.1016/0197-0186(89)90176-9

Abstract

The chromosomal gene for human phenylethanolamine N-methyltransferase (PNMT; EC 2.1.1.28) was isolated from a human genomic library using a cloned human PNMT cDNA as a probe, and the nucleotide sequence was determined. PNMT is encoded in a single gene which consists of three exons. We observed newly the presence of minor PNMT mRNA (type B) besides the major mRNA (type A) as reported previously (Kaneda et al., J. Biol. Chem. 263, 7672-7677, 1988) by Northern hybridization. Type B mRNA carries an approximately 700 nucleotide-long untranslated region in the 5? terminus. This suggests that two types of mRNA are produced from a single gene through the use of two alternative promoters. A TATA-like sequence locates 30 base pair upstream from the cap site of type A mRNA. Upstream of the cap site, there are several sequences resembling Spl binding sites and glucocorticoid responsive elements, with the latter also found in the first intron.