Literature DB >> 2872999

Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways.

S P Craig, V J Buckle, A Lamouroux, J Mallet, I Craig.   

Abstract

Phenylalanine hydroxylase (PAH) and tyrosine hydroxylase (TH) are consecutive enzymes in the metabolic pathway leading to the production of catecholamine neurotransmitters. A comparison of recently available sequence data of these enzymes in the rat indicates about 70% homology in the 3' coding regions. We have localized TH by in situ hybridization to human chromosome region 11p15. Consideration of this assignment and that of PAH to chromosome 12, together with the known distribution of other pairs of related genes on these two chromosomes, provides convincing evidence of their ancestral relationship and suggests a role for gene duplication in the diversification of metabolic pathways in the vertebrate ancestors of mammals.

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Year:  1986        PMID: 2872999     DOI: 10.1159/000132246

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  11 in total

1.  Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism.

Authors:  D A Nielsen; M Dean; D Goldman
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

2.  DraI and ScaI RFLPs at human tyrosine hydroxylase (TH) gene locus.

Authors:  K J Tinklenberg; U Masharani; R T Coleman; J Taylor; R Cawthorn; P Frossard
Journal:  Nucleic Acids Res       Date:  1988-11-25       Impact factor: 16.971

3.  Human tyrosine hydroxylase (TH) genomic fragment (pHGTH4) identifies a PstI polymorphism.

Authors:  J R Kelsoe; B K Stubblefield; E I Ginns
Journal:  Nucleic Acids Res       Date:  1988-08-11       Impact factor: 16.971

Review 4.  Structure and function of the aromatic amino acid hydroxylases.

Authors:  S E Hufton; I G Jennings; R G Cotton
Journal:  Biochem J       Date:  1995-10-15       Impact factor: 3.857

Review 5.  A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC).

Authors:  R A Wevers; J F de Rijk-van Andel; C Bräutigam; B Geurtz; L P van den Heuvel; G C Steenbergen-Spanjers; J A Smeitink; G F Hoffmann; F J Gabreëls
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

Review 6.  Tyrosine hydroxylase (TH), its cofactor tetrahydrobiopterin (BH4), other catecholamine-related enzymes, and their human genes in relation to the drug and gene therapies of Parkinson's disease (PD): historical overview and future prospects.

Authors:  Toshiharu Nagatsu; Ikuko Nagatsu
Journal:  J Neural Transm (Vienna)       Date:  2016-08-04       Impact factor: 3.575

7.  The homogentisate pathway: a central catabolic pathway involved in the degradation of L-phenylalanine, L-tyrosine, and 3-hydroxyphenylacetate in Pseudomonas putida.

Authors:  Elsa Arias-Barrau; Elías R Olivera; José M Luengo; Cristina Fernández; Beatriz Galán; José L García; Eduardo Díaz; Baltasar Miñambres
Journal:  J Bacteriol       Date:  2004-08       Impact factor: 3.490

8.  Molecular and functional characterization of amylin, a peptide associated with type 2 diabetes mellitus.

Authors:  A N Roberts; B Leighton; J A Todd; D Cockburn; P N Schofield; R Sutton; S Holt; Y Boyd; A J Day; E A Foot
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

9.  IDDM2 and the polymorphism of the human tyrosine hydroxylase (hTH) gene in African Americans with type-1 diabetes.

Authors:  Noureddine Berka; Gail Nunlee-Bland; Elhajja Erabhaoui; Maher Belmamoun; Georgia M Dunston
Journal:  J Natl Med Assoc       Date:  2004-08       Impact factor: 1.798

Review 10.  Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's disease.

Authors:  Guney Bademci; Jeffery M Vance; Liyong Wang
Journal:  CNS Neurol Disord Drug Targets       Date:  2012-06-01       Impact factor: 4.388

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