Abstract

At least four genes encode the human alkaline phosphatases (ALPs). The genes encoding three of these proteins (intestinal, placental, and placental-like ALPs), are linked on the long arm of chromosome 2, while the fourth gene (encoding liver/bone/kidney ALP) is located on chromosome 1. One of the linked genes, intestinal alkaline phosphatase, has been isolated on two overlapping phage clones and sequenced in its entirety. The gene is composed of 11 exons interrupted by 10 introns. Introns in intestinal, placental, and liver/bone/kidney ALPs occur at analogous positions (see accompanying articles), confirming that these genes arose from a single ancestral ALP gene. Multiple intestinal ALP mRNA species can be detected in RNA isolated from adult and fetal intestine and from cell line RNAs. In cell line RNA, the various species are the result of differential use of at least three of the four polyadenylation signals present in the intestinal ALP gene. A 125-base pair fragment located 5' to the first exon can function as a promoter in mammalian cells. This region contains two putative transcription signals, a TATA-like sequence and a consensus binding site for the transcription factor Sp1.

Highlights

  • At least fourgenes encode the humanalkaline phos- which they arepredominantly expressed, include the placental phatases (ALPs)

  • Placental, and liver/bone/kidney alkaline phosphatase (ALPS) occur at analogous positions, confirmingthat these genes arose from a single ancestral ALP gene

  • These membrane-bound gene gave rise to glycoproteins fall into three classes that are classically dis- the placental ALP gene

Read more

Summary

Introduction

At least fourgenes encode the humanalkaline phos- which they arepredominantly expressed, include the placental phatases (ALPs). DNA clones that contain overlapping inserts which encom- Since the gene was isolated on two different DNA fragpass the entire intestinal ALP gene, genomic DNA libraries ments, we cannot be absolutely sure that the sequence prewere constructed from normal human fibroblast DNA and sented was not derived from two separate but nearly identical screened with probes for intestinal and placental ALPs.The genes.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call