Literature DB >> 19573577

GCH1 expression in human cerebellum from healthy individuals is not gender dependent.

Christian Wider1, Sarah Lincoln, Justus C Dachsel, Gregory Kapatos, Michael G Heckman, Nancy N Diehl, Spiridon Papapetropoulos, Deborah Mash, Alex Rajput, Ali H Rajput, Dennis W Dickson, Zbigniew K Wszolek, Matthew J Farrer.   

Abstract

Dopa-responsive dystonia (DRD) is a familial childhood-onset disease characterized by fluctuating dystonia, associated with tremor and parkinsonism in some patients. In most families the disease displays autosomal dominant inheritance due to mutations in the GTP cyclohydrolase 1 gene (GCH1). Penetrance and symptom severity display strong female predominance for which gender-specific GCH1 expression has been hypothesized. In this study, GCH1 mRNA expression was measured in cerebellar tissue from 66 healthy human subjects (30 women), and in cerebellar and nigral tissue from eight individuals. No significant difference was found between men and women with small effect sizes observed. Although the correlation between cerebellar and nigral GCH1 expression remains to be further examined, this exploratory study does not support gender-specific GCH1 expression being the basis for the skewed gender distribution observed in DRD patients.

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Year:  2009        PMID: 19573577      PMCID: PMC2732187          DOI: 10.1016/j.neulet.2009.06.082

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  14 in total

1.  Normal values and age-dependent changes in GTP cyclohydrolase I activity in stimulated mononuclear blood cells measured by high-performance liquid chromatography.

Authors:  M Hibiya; H Ichinose; N Ozaki; K Fujita; T Nishimoto; T Yoshikawa; Y Asano; T Nagatsu
Journal:  J Chromatogr B Biomed Sci Appl       Date:  2000-03-31

2.  Age-related decreases in GTP-cyclohydrolase-I immunoreactive neurons in the monkey and human substantia nigra.

Authors:  E Y Chen; E Kallwitz; S E Leff; E J Cochran; E J Mufson; J H Kordower; R J Mandel
Journal:  J Comp Neurol       Date:  2000-10-30       Impact factor: 3.215

3.  High penetrance and pronounced variation in expressivity of GCH1 mutations in five families with dopa-responsive dystonia.

Authors:  D Steinberger; Y Weber; R Korinthenberg; G Deuschl; R Benecke; J Martinius; U Müller
Journal:  Ann Neurol       Date:  1998-05       Impact factor: 10.422

4.  Nigrostriatal dopamine neurons express low levels of GTP cyclohydrolase I protein.

Authors:  K Hirayama; G Kapatos
Journal:  J Neurochem       Date:  1998-01       Impact factor: 5.372

5.  GTP cyclohydrolase I gene expression in the brains of male and female hph-1 mice.

Authors:  M Shimoji; K Hirayama; K Hyland; G Kapatos
Journal:  J Neurochem       Date:  1999-02       Impact factor: 5.372

6.  Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia.

Authors:  Y Furukawa; A E Lang; J M Trugman; T D Bird; A Hunter; M Sadeh; T Tagawa; P H St George-Hyslop; M Guttman; L W Morris; O Hornykiewicz; M Shimadzu; S J Kish
Journal:  Neurology       Date:  1998-04       Impact factor: 9.910

Review 7.  Dopa-responsive dystonia.

Authors:  T G Nygaard; C D Marsden; R C Duvoisin
Journal:  Adv Neurol       Date:  1988

8.  Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene.

Authors:  H Ichinose; T Ohye; E Takahashi; N Seki; T Hori; M Segawa; Y Nomura; K Endo; H Tanaka; S Tsuji
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

9.  Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5.

Authors:  C Wider; S Melquist; M Hauf; A Solida; S A Cobb; J M Kachergus; J Gass; K D Coon; M Baker; A Cannon; D A Stephan; D F Schorderet; J Ghika; P R Burkhard; G Kapatos; M Hutton; M J Farrer; Z K Wszolek; F J G Vingerhoets
Journal:  Neurology       Date:  2007-09-05       Impact factor: 9.910

10.  Tetrahydrobiopterin biosynthesis in the rat brain: heterogeneity of GTP cyclohydrolase I mRNA expression in monoamine-containing neurons.

Authors:  S I Lentz; G Kapatos
Journal:  Neurochem Int       Date:  1996 May-Jun       Impact factor: 3.921

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