Literature DB >> 1975241

Structure of the arylsulfatase A gene.

J Kreysing1, K von Figura, V Gieselmann.   

Abstract

A 14-kb genomic clone containing the entire gene of human lysosomal arylsulfatase A was isolated. The arylsulfatase A gene is about 3.2 kb long and has eight exons (103-320 nucleotides in size). All intron-exon splice junctions conformed to the GT/AG consensus sequence. S1 nuclease mapping shows multiple transcription initiation sites between nucleotides -367 and -387. A fragment encompassing 360 nucleotides of the flanking sequence upstream of the transcription initiation site shows promoter activity when it was transiently expressed in COS cells using the gene for bacterial chloramphenicol acetyltransferase as a reporter gene. This putative promoter region shows four potential Sp1 binding sites but lacks typical TATA and CAAT box sequences. Three different mRNA species of 2.1, 3.7 and 4.8 kb are transcribed from the gene and arise probably from the use of different polyadenylation signals.

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Year:  1990        PMID: 1975241     DOI: 10.1111/j.1432-1033.1990.tb19167.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  33 in total

Review 1.  Gene transfer approaches to the lysosomal storage disorders.

Authors:  J A Barranger; E O Rice; W P Swaney
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-01-11       Impact factor: 16.971

Review 3.  A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes I: general principles and overview.

Authors:  Jian-Min Chen; Claude Férec; David N Cooper
Journal:  Hum Genet       Date:  2006-04-28       Impact factor: 4.132

Review 4.  Gene therapy for metachromatic leukodystrophy.

Authors:  Jonathan B Rosenberg; Stephen M Kaminsky; Patrick Aubourg; Ronald G Crystal; Dolan Sondhi
Journal:  J Neurosci Res       Date:  2016-11       Impact factor: 4.164

Review 5.  Molecular genetics of metachromatic leukodystrophy.

Authors:  V Gieselmann; A Polten; J Kreysing; K von Figura
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

6.  Metachromatic leukodystrophy among southern Alaskan Eskimos: molecular and genetic studies.

Authors:  N M Pastor-Soler; E M Schertz; M A Rafi; G de Gala; D A Wenger
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 7.  Metachromatic leukodystrophy: molecular genetics and an animal model.

Authors:  V Gieselmann; U Matzner; B Hess; R Lüllmann-Rauch; R Coenen; D Hartmann; R D'Hooge; P DeDeyn; G Nagels
Journal:  J Inherit Metab Dis       Date:  1998-08       Impact factor: 4.982

8.  Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population.

Authors:  Nizar Ben Halim; Imen Dorboz; Rym Kefi; Najla Kharrat; Eleonore Eymard-Pierre; Majdi Nagara; Lilia Romdhane; Nissaf Ben Alaya-Bouafif; Ahmed Rebai; Najoua Miladi; Odile Boespflug-Tanguy; Sonia Abdelhak
Journal:  Neurol Sci       Date:  2015-11-14       Impact factor: 3.307

9.  The structural basis for the electrophoretic isoforms of normal and variant human platelet arylsulphatase A.

Authors:  R D Poretz; R S Yang; B Canas; H Lackland; S Stein; P Manowitz
Journal:  Biochem J       Date:  1992-11-01       Impact factor: 3.857

10.  Prevalence of common mutations in the arylsulphatase A gene in metachromatic leukodystrophy patients diagnosed in Britain.

Authors:  M L Barth; A Fensom; A Harris
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

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