PRECURSOR PRODUCT RELATIONSHIP BETWEEN GM1 AND GD1A BIOSYNTHESIZED FROM EXOGENOUS GM2 GANGLIOSIDE IN RAT-LIVER

被引:8
|
作者
TRINCHERA, M
GHIDONI, R
机构
[1] Department of Medical Chemistry and Biochemistry, Medical School, University of Milan
来源
JOURNAL OF BIOCHEMISTRY | 1990年 / 107卷 / 04期
关键词
D O I
10.1093/oxfordjournals.jbchem.a123096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The demonstration of a precursor-product relationship in the course of GM1 and GDla biosynthesis is described in the present paper. We injected rats with GM2 gangliosides [GalNAcβ1→4<NeuAca2→3)Gal£l-→4Glcβl→1 Cer] of brain origin, which were iso-topically radiolabeled on the GalNAc ([GalNAc-3H]GM2) or sphingosine ([Sph-3H]GM2) residue. We then compared the time-courses of GM1 and GDla biosynthesis in the liver after the administration of each radiolabeled GM2 derivative. After the administration of [GalNAc-3H]GM2, GM1, and GDla were both present as doublets, that could be easily resolved on TLC. The lower spot of each doublet was identified as a species having the typical rat brain ceramide moiety and represented gangliosides formed through direct glycosylation of the injected GM2. The upper spot of each doublet was identified as a species having the typical rat liver ceramide moiety and represented gangliosides formed through recycling of the [3H] GalNAc residue, released during ganglioside catabolism. After the administration of [Sph-3H]GM2, only ganglioside with the rat brain ceramide moiety were found, that represented the sum of ganglioside formed through direct glycosylation and those formed through recycling of some sphingosine-containing fragments. In each case, the time-course of GM1 and GDla biosynthesis exhibited a precursor-product relationship. The curve obtained from the direct glycosylation showed a timing delay with respect to those obtained from recycling of GM2 fragments. These results are consistent with the hypothesis that the sequential addition of activated sugars to a sphingolipid precursor is a dissociative process, catalyzed by physically independent enzymatic activities. © 1990 COPYRIGHT, 1990 BY THE JOURNAL OF BIOCHEMISTRY.
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页码:619 / 623
页数:5
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