Molecular cloning of the sphingolipid activator protein-1 (SAP-1), the sulfatide sulfatase activator
- PMID: 2868718
- DOI: 10.1016/s0006-291x(86)80518-6
Molecular cloning of the sphingolipid activator protein-1 (SAP-1), the sulfatide sulfatase activator
Abstract
A cDNA coding for SAP-1 was isolated from a lambda gt11 human hepatoma expression library using polyclonal antibodies raised against human SAP-1. Three positive clones were isolated with inserts of approximately 0.3 Kb (S1.1), 2 Kb (S1.2) and 2.2 Kb (S-1.3). The latter 2 contained an internal EcoRI site. All three clones cross-hybridized with one another, indicating sequence homology. The nucleotide sequence of S-1.1 was determined. Colinearity was established between 19 amino acids obtained by sequencing the amino terminus of pure SAP-1 and 57 bp from the 5' end of S-1.1. The open reading frame of S-1.1 coded for 67 amino acids. One glycosylation site was found 21 residues from the amino terminus, and no stop codons were found. S-1.1 codes for a mature polypeptide chain with a calculated molecular weight of 8955 daltons, corresponding to approximately 99% of mature SAP-1.
Similar articles
-
Nucleotide sequence of cloned cDNA for human sphingolipid activator protein 1 precursor.Proc Natl Acad Sci U S A. 1987 Dec;84(23):8652-6. doi: 10.1073/pnas.84.23.8652. Proc Natl Acad Sci U S A. 1987. PMID: 2825202 Free PMC article.
-
Coding of two sphingolipid activator proteins (SAP-1 and SAP-2) by same genetic locus.Science. 1988 Aug 26;241(4869):1098-101. doi: 10.1126/science.2842863. Science. 1988. PMID: 2842863
-
Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and C.Genomics. 1990 Jan;6(1):149-58. doi: 10.1016/0888-7543(90)90460-c. Genomics. 1990. PMID: 1968043
-
[Metachromatic leukodystrophy (MLD) and Multiple sulphatase deficiency (MSD)].Nihon Rinsho. 1995 Dec;53(12):2994-3003. Nihon Rinsho. 1995. PMID: 8577048 Review. Japanese.
-
[Deficiency of arylsulfatase A activity as a basis of metachromatic leucodystrophy].Postepy Biochem. 1996;42(3):284-9. Postepy Biochem. 1996. PMID: 9036380 Review. Polish. No abstract available.
Cited by
-
Saposin A: second cerebrosidase activator protein.Proc Natl Acad Sci U S A. 1989 May;86(9):3389-93. doi: 10.1073/pnas.86.9.3389. Proc Natl Acad Sci U S A. 1989. PMID: 2717620 Free PMC article.
-
A triple-binding-domain model explains the specificity of the interaction of a sphingolipid activator protein (SAP-1) with sulphatide, GM1-ganglioside and globotriaosylceramide.Biochem J. 1986 Dec 15;240(3):921-4. doi: 10.1042/bj2400921. Biochem J. 1986. PMID: 3827882 Free PMC article.
-
Insertion in the mRNA of a metachromatic leukodystrophy patient with sphingolipid activator protein-1 deficiency.Proc Natl Acad Sci U S A. 1990 Feb;87(4):1426-30. doi: 10.1073/pnas.87.4.1426. Proc Natl Acad Sci U S A. 1990. PMID: 1689485 Free PMC article.
-
Correction of sulfatide metabolism after transfer of prosaposin cDNA to cultured cells from a patient with SAP-1 deficiency.Am J Hum Genet. 1992 Jun;50(6):1252-8. Am J Hum Genet. 1992. PMID: 1350885 Free PMC article.
-
The protective role of prosaposin and its receptors in the nervous system.Brain Res. 2014 Oct 17;1585:1-12. doi: 10.1016/j.brainres.2014.08.022. Epub 2014 Aug 15. Brain Res. 2014. PMID: 25130661 Free PMC article. Review.
Publication types
MeSH terms
Substances
Associated data
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous