Literature DB >> 8892025

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

S Kemp1, P A Mooyer, P A Bolhuis, B M van Geel, J L Mandel, P G Barth, P Aubourg, R J Wanders.   

Abstract

The adrenoleukodystrophy gene encodes a peroxisomal integral membrane protein (ALDP) consisting of 745 amino acids with a molecular weight of 75kDa. ALDP expression was studied in fibroblasts from 24 male ALD patients from 17 unrelated ALD kindreds. In four kindreds an identical 2-base-pair deletion was found. We report the absence of ALDP in 12 kindreds carrying nonsense mutations, frame shifts or amino acid substitutions in the carboxy terminus of ALDP, together accounting for 71% of the ALD kindreds. ALDP was present in five kindreds (29%) with amino acid substitutions in the amino terminal half of the protein; in two of these kindreds ALDP was present although at a reduced level. The absence of truncated proteins suggests that the carboxy terminus has a function in the stabilization of ALDP.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8892025     DOI: 10.1007/bf01799844

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  18 in total

1.  Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.

Authors:  R J Wanders; C W van Roermund; M J van Wijland; J Heikoop; R B Schutgens; A W Schram; J M Tager; H van den Bosch; B T Poll-Thé; J M Saudubray
Journal:  Clin Chim Acta       Date:  1987-07-15       Impact factor: 3.786

2.  Human genetics. Penetrating the peroxisome.

Authors:  D Valle; J Gärtner
Journal:  Nature       Date:  1993-02-25       Impact factor: 49.962

3.  Two intronic mutations in the adrenoleukodystrophy gene.

Authors:  S Kemp; M J Ligtenberg; B M van Geel; P G Barth; C O Sarde; B A van Oost; P A Bolhuis
Journal:  Hum Mutat       Date:  1995       Impact factor: 4.878

4.  Phenotypic heterogeneity of an adult form of adrenoleukodystrophy in monozygotic twins.

Authors:  G Sobue; I Ueno-Natsukari; H Okamoto; T A Connell; I Aizawa; K Mizoguchi; M Honma; G Ishikawa; T Mitsuma; N Natsukari
Journal:  Ann Neurol       Date:  1994-12       Impact factor: 10.422

5.  Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts.

Authors:  R J Wanders; S Denis; J P Ruiter; R B Schutgens; C W van Roermund; B S Jacobs
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

6.  Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations.

Authors:  S Kemp; M J Ligtenberg; B M van Geel; P G Barth; R A Wolterman; F Schoute; C O Sarde; J L Mandel; B A van Oost; P A Bolhuis
Journal:  Biochem Biophys Res Commun       Date:  1994-07-29       Impact factor: 3.575

7.  Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.

Authors:  J Gärtner; H Moser; D Valle
Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

8.  Predictions of a 2-locus model for disease heterogeneity: application to adrenoleukodystrophy.

Authors:  N E Maestri; T H Beaty
Journal:  Am J Med Genet       Date:  1992-11-15

9.  Altered expression of ALDP in X-linked adrenoleukodystrophy.

Authors:  P A Watkins; S J Gould; M A Smith; L T Braiterman; H M Wei; F Kok; A B Moser; H W Moser; K D Smith
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

10.  Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy.

Authors:  N Cartier; C O Sarde; A M Douar; J Mosser; J L Mandel; P Aubourg
Journal:  Hum Mol Genet       Date:  1993-11       Impact factor: 6.150

View more
  10 in total

Review 1.  Disorders related to peroxisomal membranes.

Authors:  J Gärtner
Journal:  J Inherit Metab Dis       Date:  2000-05       Impact factor: 4.982

Review 2.  X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy.

Authors:  B M van Geel; J Assies; R J Wanders; P G Barth
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-07       Impact factor: 10.154

Review 3.  X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.

Authors:  K D Smith; S Kemp; L T Braiterman; J F Lu; H M Wei; M Geraghty; G Stetten; J S Bergin; J Pevsner; P A Watkins
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

4.  X-linked adrenoleukodystrophy: improved prenatal diagnosis using both biochemical and immunological methods.

Authors:  R J Wanders; P W Mooyer; C Dekker; P Vreken
Journal:  J Inherit Metab Dis       Date:  1998-06       Impact factor: 4.982

Review 5.  X-linked adrenoleukodystrophy: pathogenesis and treatment.

Authors:  Marc Engelen; Stephan Kemp; Bwee-Tien Poll-The
Journal:  Curr Neurol Neurosci Rep       Date:  2014-10       Impact factor: 5.081

Review 6.  Adrenoleukodystrophy - neuroendocrine pathogenesis and redefinition of natural history.

Authors:  Stephan Kemp; Irene C Huffnagel; Gabor E Linthorst; Ronald J Wanders; Marc Engelen
Journal:  Nat Rev Endocrinol       Date:  2016-06-17       Impact factor: 43.330

7.  Bezafibrate lowers very long-chain fatty acids in X-linked adrenoleukodystrophy fibroblasts by inhibiting fatty acid elongation.

Authors:  Marc Engelen; Martin J A Schackmann; Rob Ofman; Robert-Jan Sanders; Inge M E Dijkstra; Sander M Houten; Stéphane Fourcade; Aurora Pujol; Bwee Tien Poll-The; Ronald J A Wanders; Stephan Kemp
Journal:  J Inherit Metab Dis       Date:  2012-03-24       Impact factor: 4.982

8.  Mutagenesis separates ATPase and thioesterase activities of the peroxisomal ABC transporter, Comatose.

Authors:  David J Carrier; Carlo W T van Roermund; Theresia A Schaedler; Hong Lin Rong; Lodewijk IJlst; Ronald J A Wanders; Stephen A Baldwin; Hans R Waterham; Frederica L Theodoulou; Alison Baker
Journal:  Sci Rep       Date:  2019-07-19       Impact factor: 4.379

9.  Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-Factor.

Authors:  Rinse W Barendsen; Inge M E Dijkstra; Wouter F Visser; Mariëlle Alders; Jet Bliek; Anita Boelen; Marelle J Bouva; Saskia N van der Crabben; Ellen Elsinghorst; Ankie G M van Gorp; Annemieke C Heijboer; Mandy Jansen; Yorrick R J Jaspers; Henk van Lenthe; Ingrid Metgod; Christiaan F Mooij; Elise H C van der Sluijs; A S Paul van Trotsenburg; Rendelien K Verschoof-Puite; Frédéric M Vaz; Hans R Waterham; Frits A Wijburg; Marc Engelen; Eugènie Dekkers; Stephan Kemp
Journal:  Front Cell Dev Biol       Date:  2020-06-17

10.  Biochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the ABCD1 Gene.

Authors:  Stephanie I W van de Stadt; Petra A W Mooyer; Inge M E Dijkstra; Conny J M Dekker; Divya Vats; Moin Vera; Maura R Z Ruzhnikov; Keith van Haren; Nelson Tang; Klaas Koop; Michel A Willemsen; Joannie Hui; Frédéric M Vaz; Merel S Ebberink; Marc Engelen; Stephan Kemp; Sacha Ferdinandusse
Journal:  Genes (Basel)       Date:  2021-11-30       Impact factor: 4.096

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.