Literature DB >> 2753159

Isolation of a cDNA encoding the human GM2 activator protein.

M Schröder1, H Klima, T Nakano, H Kwon, L E Quintern, S Gärtner, K Suzuki, K Sandhoff.   

Abstract

The GM2 activator protein is a glycolipid-binding protein required for the lysosomal degradation of ganglioside GM2. A human fibroblast cDNA library was screened with mixtures of oligonucleotide probes corresponding to four different areas of the amino acid sequence. A putative clone (821 bp) which gave positive signals to all four probe mixtures was purified and sequenced. The sequence was colinear with the sequence of 160 amino acids of the mature GM2 activator protein. Availability of the cDNA clone should facilitate investigation into function of the GM2 activator protein and also into genetic abnormalities underlying GM2 gangliosidosis AB variant.

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Year:  1989        PMID: 2753159     DOI: 10.1016/0014-5793(89)81454-1

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  17 in total

1.  Evidence for two cDNA clones encoding human GM2-activator protein.

Authors:  S Nagarajan; H C Chen; S C Li; Y T Li; J M Lockyer
Journal:  Biochem J       Date:  1992-03-15       Impact factor: 3.857

Review 2.  The early and late processing of lysosomal enzymes: proteolysis and compartmentation.

Authors:  A Hasilik
Journal:  Experientia       Date:  1992-02-15

3.  Cloning and sequence analysis of a cDNA clone coding for the mouse GM2 activator protein.

Authors:  G Bellachioma; J L Stirling; A Orlacchio; T Beccari
Journal:  Biochem J       Date:  1993-08-15       Impact factor: 3.857

4.  Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological study.

Authors:  W Schlote; K Harzer; H Christomanou; B C Paton; B Kustermann-Kuhn; B Schmid; J Seeger; U Beudt; I Schuster; U Langenbeck
Journal:  Eur J Pediatr       Date:  1991-06       Impact factor: 3.183

5.  Over-expression of a functionally active human GM2-activator protein in Escherichia coli.

Authors:  H Klima; A Klein; G van Echten; G Schwarzmann; K Suzuki; K Sandhoff
Journal:  Biochem J       Date:  1993-06-01       Impact factor: 3.857

6.  Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disorders.

Authors:  B Schmid; B C Paton; K Sandhoff; K Harzer
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

7.  Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase.

Authors:  B C Paton; B Schmid; B Kustermann-Kuhn; A Poulos; K Harzer
Journal:  Biochem J       Date:  1992-07-15       Impact factor: 3.857

8.  Effect of structural modifications of ganglioside GM2 on intra-molecular carbohydrate-to-carbohydrate interaction and enzymatic susceptibility.

Authors:  Yu-Teh Li; Su-Chen Li; Makoto Kiso; Hideharu Ishida; Laura Mauri; Laura Raimondi; Anna Bernardi; Sandro Sonnino
Journal:  Biochim Biophys Acta       Date:  2007-10-05

9.  Molecular genetics of GM2-gangliosidosis AB variant: a novel mutation and expression in BHK cells.

Authors:  M Schröder; D Schnabel; R Hurwitz; E Young; K Suzuki; K Sandhoff
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

10.  Structural organization and expression of the gene for the mouse GM2 activator protein.

Authors:  C Bertoni; M G Appolloni; J L Stirling; S C Li; Y T Li; A Orlacchio; T Beccari
Journal:  Mamm Genome       Date:  1997-02       Impact factor: 2.957

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