Literature DB >> 6946513

Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qter.

A L Wang, F X Arredondo-Vega, P F Giampietro, M Smith, W F Anderson, R J Desnick.   

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.

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Year:  1981        PMID: 6946513      PMCID: PMC348846          DOI: 10.1073/pnas.78.9.5734

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  42 in total

1.  Induction of the synthesis of delta-aminolevulinic acid synthetase in liver parenchyma cells in culture by chemical that induce acute porphyria.

Authors:  S GRANICK
Journal:  J Biol Chem       Date:  1963-06       Impact factor: 5.157

2.  The enzymatic synthesis of porphyrins from porphobilinogen. I. Uroporphyrin I.

Authors:  L BOGORAD
Journal:  J Biol Chem       Date:  1958-08       Impact factor: 5.157

3.  Quinacrine fluorescence for identifying metaphase chromosomes, with special reference to photomicrography.

Authors:  W R Breg
Journal:  Stain Technol       Date:  1972-03

4.  Intermittent acute porphyria--demonstration of a genetic defect in porphobilinogen metabolism.

Authors:  U A Meyer; L J Strand; M Doss; A C Rees; H S Marver
Journal:  N Engl J Med       Date:  1972-06-15       Impact factor: 91.245

5.  The serum porphobilinogen and hepatic porphobilinogen deaminase in normal and porphyric individuals.

Authors:  K Miyagi; R Cardinal; I Bossenmaier; C J Watson
Journal:  J Lab Clin Med       Date:  1971-11

6.  Synthesis of delta-aminolaevulinate synthase in vitro using hepatic mRNA from chick embryos with induced porphyria.

Authors:  J D Brooker; B K May; W H Elliott
Journal:  Eur J Biochem       Date:  1980-05

7.  The induction in vitro of the synthesis of delta-aminolevulinic acid synthetase in chemical porphyria: a response to certain drugs, sex hormones, and foreign chemicals.

Authors:  S Granick
Journal:  J Biol Chem       Date:  1966-03-25       Impact factor: 5.157

8.  Genetics of somatic mammalian cells: demonstration of a human esterase activator gene linked to the adeB gene.

Authors:  F T Kao; T T Puck
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

9.  Genetics of human-mouse somatic cell hybrids: linkage of human genes for lactate dehydrogenase-A and esterase-A 4 .

Authors:  T B Shows
Journal:  Proc Natl Acad Sci U S A       Date:  1972-02       Impact factor: 11.205

10.  Decreased red cell uroporphyrinogen I synthetase activity in intermittent acute porphyria.

Authors:  L J Strand; U A Meyer; B F Felsher; A G Redeker; H S Marver
Journal:  J Clin Invest       Date:  1972-10       Impact factor: 14.808

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  20 in total

1.  Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2----q26.3.

Authors:  K H Astrin; C A Warner; H W Yoo; P J Goodfellow; S F Tsai; R J Desnick
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

2.  A MspI polymorphism for the human porphobilinogen deaminase gene.

Authors:  D H Llewellyn; N A Kalsheker; G H Elder; P R Harrison; S Chretien; M Goossens
Journal:  Nucleic Acids Res       Date:  1987-02-11       Impact factor: 16.971

3.  DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria.

Authors:  J S Lee; M Anvret; J Lindsten; L Lannfelt; P Gellerfors; L Wetterberg; Y Floderus; S Thunell
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

Review 4.  Heme biosynthesis and the porphyrias.

Authors:  John D Phillips
Journal:  Mol Genet Metab       Date:  2019-04-22       Impact factor: 4.797

5.  Molecular genetics of acute intermittent porphyria.

Authors:  A Goldberg
Journal:  Br Med J (Clin Res Ed)       Date:  1985-08-24

6.  Acute intermittent porphyria: characterization of a novel mutation in the structural gene for porphobilinogen deaminase. Demonstration of noncatalytic enzyme intermediates stabilized by bound substrate.

Authors:  R J Desnick; L T Ostasiewicz; P A Tishler; P Mustajoki
Journal:  J Clin Invest       Date:  1985-08       Impact factor: 14.808

7.  A PstI polymorphism for the human porphobilinogen deaminase gene (PBG).

Authors:  J S Lee; M Anvret
Journal:  Nucleic Acids Res       Date:  1987-08-11       Impact factor: 16.971

8.  Localization of the structural gene for human apolipoprotein A-I on the long arm of human chromosome 11.

Authors:  P Cheung; F T Kao; M L Law; C Jones; T T Puck; L Chan
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205

9.  Acute intermittent porphyria: identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal expression of the erythroid-specific enzyme.

Authors:  C H Chen; K H Astrin; G Lee; K E Anderson; R J Desnick
Journal:  J Clin Invest       Date:  1994-11       Impact factor: 14.808

Review 10.  Porphobilinogen deaminase gene structure and molecular defects.

Authors:  J C Deybach; H Puy
Journal:  J Bioenerg Biomembr       Date:  1995-04       Impact factor: 2.945

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