Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qter.
Open Access
- 1 September 1981
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 78 (9) , 5734-5738
- https://doi.org/10.1073/pnas.78.9.5734
Abstract
The regional gene assignments for human porphobilinogen deaminase (PBGD; EC 4.3.1.8) and esterase A4 (ESA4; EC3.1.1.1) chromosome 11 have been determined with somatic cell hybridization and immunologic, electrophoretic, and cytogenetic techniques. Dimethyl sulfoxide-induced erythroid differentiation of hybrid clones derived from the fusion of tetraploid Friend murine erythroleukemia (2S MEL) cells deficient in thymidine kinase and human Lesch--Nyhan fibroblasts (HLN) deficient in hypoxanthine phosphoribosyltransferase (HPRT-; EC 2.4.2.8) were examined for expression of human PBGD, ESA4, and lactate dehydrogenase A (LDHA; EC 1.1.1.27). Human PBGD was detected by rocket immunoelectrophoresis with rabbit anti-human PBGD IgG and by isoelectric focusing. The human chromosome complement of each clone was determined by cytogenetic and enzyme marker analyses. Of the five primary 2S MEL--HLN clones examined, three were positive for human PBGD. These were subcloned to yield a total of 10 secondary, tertiary, or quaternary clones. Analyses of these subclones permitted the regional assignment of human PBGD and ESA4 to the long arm of chromosome 11. Finer regional assignment of the loci for human PBGD and ESA4 was facilitated when two 2S MEL (HPRT-)--human fibroblast (HX/11) hybrids, each containing the X chromosome--autosome translocation (der11), t(X;11)(q25-26;q23) as the only human chromosome, were examined for expression of human PBGD, ESA4, and LDHA. One clone, HX/11-2, contained the intact X/11 translocated chromosome; in the other, HX/11-3, 11p was deleted, and the human X/11 derivative was translocated onto a mouse chromosome. HX/11-2 expressed human LDHA, but HX/11-3 did not, verifying that the latter human 11/X derivative did not include 11pter leads to 11p12; PBGD and ESA4 were not detected in either hybrid. These results confirm the location of the gene for human PBGD on chromosome 11 and establish the assignment of the loci for PBGD and ESA4 in the region 11q23 leads to 11qter.This publication has 43 references indexed in Scilit:
- Synthesis of δ‐Aminolaevulinate Synthase in vitro Using Hepatic mRNA from Chick Embryos with Induced PorphyriaEuropean Journal of Biochemistry, 1980
- Genetics of Somatic Mammalian Cells: Demonstration of a Human Esterase Activator Gene Linked to the AdeB GeneProceedings of the National Academy of Sciences, 1972
- Decreased Red Cell Uroporphyrinogen I Synthetase Activity in Intermittent Acute PorphyriaJournal of Clinical Investigation, 1972
- Intermittent Acute Porphyria — Demonstration of a Genetic Defect in Porphobilinogen MetabolismNew England Journal of Medicine, 1972
- Genetics of Human-Mouse Somatic Cell Hybrids: Linkage of Human Genes for Lactate Dehydrogenase- A and Esterase-A 4Proceedings of the National Academy of Sciences, 1972
- Quinacrine Fluorescence for Identifying Metaphase Chromosomes, with Special Reference to PhotomicrographyStain Technology, 1972
- The serum porphobilinogen and hepatic porphobilinogen deaminase in normal and porphyric individuals.1971
- INDUCTION IN VITRO OF SYNTHESIS OF DELTA-AMINOLEVULINIC ACID SYNTHETASE IN CHEMICAL PORPHYRIA - A RESPONSE TO CERTAIN DRUGS SEX HORMONES AND FOREIGN CHEMICALS1966
- Induction of the synthesis of delta-aminolevulinic acid synthetase in liver parenchyma cells in culture by chemical that induce acute porphyria.1963
- ENZYMATIC SYNTHESIS OF PORPHYRINS FROM PORPHOBILINOGEN .1. UROPORPHYRIN-I1958