δ-Aminolevulinate dehydratase: Induced expression and regional assignment of the human gene to chromosome 9q13»qter

✍ Scribed by A. -L. Wang; K. H. Astrin; W. F. Anderson; R. J. Desnick

• Publisher: Springer
• Year: 1985
• Tongue: English
• Weight: 471 KB
• Volume: 70
• Category: Article
• ISSN: 0340-6717
• DOI: 10.1007/bf00389449

✦ Synopsis

The structural gene encoding human 5-aminolevulinate dehydratase has been assigned to the long arm of chromosome 9 by somatic cell hybridization techniques using murine erythroleukemia-human fibroblast somatic cell hybrids. Dimethyl sulfoxide induction of erythroid differentiation in these hybrid cells resulted in a 3 to 12-fold increase in the levels of total g-aminolevulinate dehydratase. Human 6aminolevulinate dehydratase was detected by an immunodiscrimination assay using polyclonal mouse anti-human 6aminolevulinate dehydratase antibodies. Of four primary hybrid clones, each from an independent fusion, one hybrid line, XX-8, was positive for human 8-aminolevulinate dehydratase. Examination of 23 secondary, tertiary, and quaternary XX-8 subclones revealed that the expression of the human isozyme segregated with human chromosome 9q, confirming the provisional regional assignment made by classical linkage studies. One positive quaternary clone, XX-8-H21-H7-2, expressed human 8-aminolevulinate dehydratase activity and contained only human 9q13~qter. In addition, studies of tertiary and quaternary subclones from two series, XX-8-A31 and XX-8-H21-H7, indicated that murine regulatory factors increased the human as well as the murine enzymatic activity following induction of erythroid differentiation.