Literature DB >> 3041403

Immunoblot detection of enzyme proteins of peroxisomal beta-oxidation in fibroblasts, amniocytes, and chorionic villous cells. Possible marker for prenatal diagnosis of Zellweger's syndrome.

N Shimozawa1, Y Suzuki, T Orii, T Hashimoto.   

Abstract

The amounts of enzyme proteins of peroxisomal beta-oxidation in fibroblasts and chorionic villous cells from infants with Zellweger syndrome and in fibroblasts, amniocytes, and chorionic villi from healthy controls were measured by immunoblot analysis. Immunoreactive proteins of peroxisomal acyl-CoA oxidase and 3-ketoacyl-CoA thiolase were absent in fibroblasts and chorionic villous cells from the patients, yet these enzyme proteins were present in fibroblasts, cultured amniocytes, and chorionic villi from the normal controls. These results show that immunoblot analysis of peroxisomal beta-oxidation enzymes in amniocytes and chorionic villous cells is of potential value for the prenatal detection of Zellweger syndrome.

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Year:  1988        PMID: 3041403     DOI: 10.1002/pd.1970080407

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  6 in total

Review 1.  Prenatal diagnosis of enzyme defects.

Authors:  B Winchester
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791

Review 2.  The inborn errors of peroxisomal beta-oxidation: a review.

Authors:  R J Wanders; C W van Roermund; R B Schutgens; P G Barth; H S Heymans; H van den Bosch; J M Tager
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

Authors:  J C Heikoop; C W van Roermund; W W Just; R Ofman; R B Schutgens; H S Heymans; R J Wanders; J M Tager
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

4.  Peroxisomal 3-ketoacyl-CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata.

Authors:  Y Suzuki; N Shimozawa; K Izai; Y Uchida; K Miura; H Akatsuka; M Nagaya; S Yamaguchi; T Orii
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

Review 5.  Prenatal diagnosis of inherited metabolic diseases.

Authors:  R Diukman; J D Goldberg
Journal:  West J Med       Date:  1993-09

6.  Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.

Authors:  C W van Roermund; S Brul; J M Tager; R B Schutgens; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

  6 in total

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