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Physiological Exploration of the Long Term Evolutionary Selection against Expression of N-Glycolylneuraminic Acid in the Brain.

Authors :
Yuko Naito-Matsui
Davies, Leela R. L.
Hiromu Takematsu
Hsun-Hua Chou
Pam Tangvoranuntakul
Carlin, Aaron F.
Verhagen, Andrea
Heyser, Charles J.
Seung-Wan Yoo
Choudhury, Biswa
Paton, James C.
Paton, Adrienne W.
Varki, Nissi M.
Schnaar, Ronald L.
Varki, Ajit
Source :
Journal of Biological Chemistry. 2/17/2017, Vol. 292 Issue 7, p2557-2570. 14p.
Publication Year :
2017

Abstract

All vertebrate cell surfaces display a dense glycan layer often terminated with sialic acids, which have multiple functions due to their location and diverse modifications. The major sialic acids in most mammalian tissues are N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc), the latter being derived from Neu5Ac via addition of one oxygen atom at the sugar nucleotide level by CMP-Neu5Ac hydroxylase (Cmah). Contrasting with other organs that express various ratios of Neu5Ac and Neu5Gc depending on the variable expression of Cmah, Neu5Gc expression in the brain is extremely low in all vertebrates studied to date, suggesting that neural expression is detrimental to animals. However, physiological exploration of the reasons for this long term evolutionary selection has been lacking. To explore the consequences of forced expression of Neu5Gc in the brain, we have established brain-specificCmah transgenic mice. Such Neu5Gc overexpression in the brain resulted in abnormal locomotor activity, impaired object recognition memory, and abnormal axon myelination. Brain-specific Cmah transgenic mice were also lethally sensitive to a Neu5Gcpreferring bacterial toxin, even though Neu5Gc was overexpressed only in the brain and other organs maintained endogenous Neu5Gc expression, as in wild-type mice. Therefore, the unusually strict evolutionary suppression of Neu5Gc expression in the vertebrate brain may be explained by evasion of negative effects on neural functions and by selection against pathogens. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219258
Volume :
292
Issue :
7
Database :
Academic Search Index
Journal :
Journal of Biological Chemistry
Publication Type :
Academic Journal
Accession number :
121383217
Full Text :
https://doi.org/10.1074/jbc.M116.768531