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Cloning and transcriptional regulation of genes responsible for synthesis of gangliosides

  • Guichao Zeng
    ,
  • Robert K. Yu(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Abstract

Ganglioside synthases are glycosyltransferases involved in the biosynthesis of glycoconjugates. A number of ganglioside synthase genes have been cloned and characterized. They are classified into different families of glycosyl-transferases based on similarities of their amino acid sequences. Tissue-specific expression of these genes has been analyzed by hybridization using cDNA fragments. Enzymatic characterization with the expressed recombinant enzymes showed these enzymes differ in their donor and acceptor substrate specificities and other biochemical parameters. In vitro enzymatic analysis also showed that one linkage can be synthesized by multiple enzymes and one enzyme may be responsible for synthesis of multiple gangliosides. Following the cloning of the ganglioside synthase genes, the promoters of the key synthase genes in the ganglioside biosynthetic pathway have been cloned and analyzed. All of thd promoters are TATA-less, lacking a CCAAT box but containing GC-rich boxes, characteristic of the house-keeping genes, although transcription of ganglioside synthase genes is subject to complex developmental and tissue-specific regulation. A set of cis-acting elements and transcription factors, including Sp1, AP2, and CREB, function in the proximal promoters, Negative-regulatory regions have also been defined in most of the promoters. We present here an overview of these genes and their transcriptional regulation.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 317-324 (8 pages)

Journal (Volume, Issue Number)

Current drug targets (Volume 9, Issue 4)

Publication milestones

  • Published - 04/2008

Publication status

Published - 04/2008

ISSN

1389-4501

Publication IDs

  • Scopus: 42949174061
  • PubMed: 18393825

Publication metrics

Metrics

SciVal
citations
19
SciVal
FWCI
0.53
SciVal
Author count
2
SciVal
Paper percentile
73
Scopus
citations
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1

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Citation count
26
Captures
16

Funding Details

FunderFunding number
NINDS
R01NS011853