A developmental change in dolichyl phosphate mannose synthase activity in pig brain
- PMID: 7396876
- PMCID: PMC1161892
- DOI: 10.1042/bj1880481
A developmental change in dolichyl phosphate mannose synthase activity in pig brain
Abstract
The initial rate of dolichyl phosphate mannose biosynthesis was measured in white-matter membranes from pig brain at various ages from before birth throughout the period of most rapid brain development. Dolichyl phosphate mannose synthase activity increased from prenatal values to a maximum in 3 week-old animals, and gradually decreased to adult values after 8 weeks of age. The nature of the developmental change was investigated by enzymic and biochemical comparisons of the membrane preparations from the most active age (3 weeks) and adult controls. The specific activity of dolichyl phosphate mannose synthase in preparations from actively myelinating animals was approx. 3-fold higher than adults when mannolipid formation was assayed with saturating concentrations of GDP-[(14)C]mannose and utilizing only endogenous acceptor lipid. No major variations were found in the apparent K(m) values for GDP-mannose or exogenous dolichyl monophosphate. However, the ratio of dolichyl phosphate mannose synthase activity for myelinating animals/adult animals decreased significantly when large amounts of exogenous dolichyl monophosphate were added to the incubation mixtures. Dolichyl phosphate mannose synthase activity was also compared in white-matter membranes depleted of endogenous dolichyl monophosphate by enzymic mannosylation or treatment with butanol. When these preparations were assayed with identical amounts of exogenous dolichyl monophosphate, the dolichyl monophosphate-depleted membranes from actively myelinating animals contained only 20-30% more dolichyl phosphate mannose synthase activity. Overall, these studies strongly suggest that the developmental change in dolichyl phosphate mannose synthase activity is due primarily to the presence of a relatively lower amount of endogenous dolichyl monophosphate being accessible to the mannosyltransferase in the white-matter membranes from adult animals.
Similar articles
-
Factors affecting glucosyl and mannosyl transfer to dolichyl monophosphate by liver cell-free preparations.Eur J Biochem. 1978 Feb;83(2):581-6. doi: 10.1111/j.1432-1033.1978.tb12126.x. Eur J Biochem. 1978. PMID: 631137
-
Glycoprotein biosynthesis: studies on thyroid mannosyltransferases. II. Characterization of a polyisoprenyl mannosyl phosphate and evaluation of its intermediary role in the glycosylation of exogenous acceptors.J Biol Chem. 1975 Apr 25;250(8):2842-54. J Biol Chem. 1975. PMID: 16509041
-
Dietary effects on the formation of dolichyl monophosphate mannose by microsomal preparations of rat adiopose tissue.Biochem J. 1980 Mar 15;186(3):791-8. doi: 10.1042/bj1860791. Biochem J. 1980. PMID: 7396837 Free PMC article.
-
The role of polyprenol-linked sugars in eukaryotic macromolecular synthesis.Biochem Soc Trans. 1977;5(6):1682-7. doi: 10.1042/bst0051682. Biochem Soc Trans. 1977. PMID: 340300 Review. No abstract available.
-
The dolichol pathway in the retina and its involvement in the glycosylation of rhodopsin.Biochim Biophys Acta. 1999 Dec 27;1473(2-3):272-85. doi: 10.1016/s0304-4165(99)00198-1. Biochim Biophys Acta. 1999. PMID: 10594365 Review. No abstract available.
Cited by
-
A differentiation-dependent polyisoprenol kinase in Dictyostelium discoideum.Mol Cell Biochem. 1982 Oct 29;48(3):183-9. doi: 10.1007/BF00421227. Mol Cell Biochem. 1982. PMID: 6294493
-
Phosphorylated dolichols in aging.Biochem J. 1990 Feb 1;265(3):891-4. doi: 10.1042/bj2650891. Biochem J. 1990. PMID: 2306221 Free PMC article.
-
Glycoprotein synthesis in explants of developing rabbit mammary gland in culture.Biochem J. 1981 Sep 15;198(3):683-90. doi: 10.1042/bj1980683. Biochem J. 1981. PMID: 7326034 Free PMC article.
-
Saccharomyces cerevisiae sec59 cells are deficient in dolichol kinase activity.Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):7013-6. doi: 10.1073/pnas.89.15.7013. Proc Natl Acad Sci U S A. 1992. PMID: 1323123 Free PMC article.
-
Postnatal changes in dolichol-pathway enzyme activities in cerebral cortex neurons.Biochem J. 1982 Jan 15;202(1):87-95. doi: 10.1042/bj2020087. Biochem J. 1982. PMID: 6211172 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources