SEQUENCE-ANALYSIS OF A CDNA FOR LYSYL HYDROXYLASE ISOLATED FROM HUMANSKIN FIBROBLASTS FROM A NORMAL DONOR - DIFFERENCES FROM HUMAN PLACENTAL LYSYL HYDROXYLASE CDNA
Hn. Yeowell et al., SEQUENCE-ANALYSIS OF A CDNA FOR LYSYL HYDROXYLASE ISOLATED FROM HUMANSKIN FIBROBLASTS FROM A NORMAL DONOR - DIFFERENCES FROM HUMAN PLACENTAL LYSYL HYDROXYLASE CDNA, Journal of investigative dermatology, 102(3), 1994, pp. 382-384
Using polymerase chain reaction, we have isolated and sequenced a 3-kb
cDNA for lysyl hydroxylase (LH) from human skin fibroblasts from an n
ormal donor. Apart from two polymorphic sites, no differences were obs
erved between the 2184 nt coding regions of LH cDNA from fibroblasts a
nd placenta. However, four differences were observed in the 3' non-cod
ing regions of the two cDNAs; three were single base changes and the f
ourth a deletion of a single base. The absence of the single nucleotid
e in the LH cDNA from fibroblasts resulted in the loss of an HpaII sit
e that is present in the placental LH cDNA; this was confirmed in HpaI
I digests of fibroblast and placental LH cDNAs from the same donor. No
rthern blots showed that the LH gene was strongly expressed in fibrobl
asts and Placenta and, to a lesser extent, in aortal lung, vein, carti
lage, and artery.