N-glycolylneuraminic acid conjugates: Implications of their absence in mammalian biochemistry

被引:0
作者
Mwangi, DW [1 ]
Bansal, DD [1 ]
机构
[1] Panjab Univ, Dept Biochem, Chandigarh 160014, India
关键词
cell adhesion molecules; glycolipids; glycoproteins; N-acetylneuraminic acid; N-acetylneuraminic acid hydroxylase; N-glycolylneuraminic acid; tumour; inflammatory disease; sialic acid;
D O I
暂无
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
N-glycolylneuraminic acid (Neu5Gc) is one of the two most common forms of sialic acids present in glycoproteins and glycolipids of mammalian tissues. It is synthesized from the most ubiquitous sialic acid, N-acetylneuraminic acid (Neu5Ac) in a hydroxylation reaction catalysed by the enzyme Neu5Ac hydroxylase. Though Neu5Gc conjugates are prevalent in many tissues of mammals, they are absent in glycolipids and only trace amounts are present in glycoproteins of the brain and central nervous system. In humans Neu5Ac is the main sialic acid as Neu5Ac hydroxylase is inactive due to mutation of its gene. The importance of sialic acids in biochemical phenomena and the distinct roles played by specific forms of these amino sugars is adequately reflected in functional studies of selectin and sialoadhesin families of adhesion molecules. The absence of Neu5Gc, therefore, in tissues of humans and brain of mammals has raised interest, especially with regard to its impact on biochemical differences evident between. humans and other mammals. It is suggested that though Neu5Gc conjugates are important in cellular interactions, their presence in brain and the central nervous system is deleterious to the latter's normal functions. Their interaction with other cellular components to form supramolecular associations is indicated that may have a bearing on major biochemical differences, a few of which are presently evident between humans and other mammals.
引用
收藏
页码:217 / 225
页数:9
相关论文
共 98 条
  • [1] Chemical diversity in the sialic acids and related α-keto acids:: An evolutionary perspective
    Angata, T
    Varki, A
    [J]. CHEMICAL REVIEWS, 2002, 102 (02) : 439 - 469
  • [2] THE P-SELECTIN GLYCOPROTEIN LIGAND FUNCTIONS AS A COMMON HUMAN-LEUKOCYTE LIGAND FOR P-SELECTINS AND E-SELECTINS
    ASA, D
    RAYCROFT, L
    MA, L
    AEED, PA
    KAYTES, PS
    ELHAMMER, AP
    GENG, JG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (19) : 11662 - 11670
  • [3] BINDING OF L-SELECTIN TO THE VASCULAR SIALOMUCIN CD34
    BAUMHUETER, S
    SINGER, MS
    HENZEL, W
    HEMMERICH, S
    RENZ, M
    ROSEN, SD
    LASKY, LA
    [J]. SCIENCE, 1993, 262 (5132) : 436 - 438
  • [4] IDENTIFICATION OF AN INDUCIBLE ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE
    BEVILACQUA, MP
    POBER, JS
    MENDRICK, DL
    COTRAN, RS
    GIMBRONE, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) : 9238 - 9242
  • [5] BOUHOURS D, 1988, J BIOL CHEM, V263, P15540
  • [6] Loss of N-glycolylneuraminic acid in human evolution -: Implications for sialic acid recognition by siglecs
    Brinkman-Van der Linden, ECM
    Sjoberg, ER
    Juneja, LR
    Crocker, PR
    Varki, N
    Varki, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) : 8633 - 8640
  • [7] A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence
    Chou, HH
    Takematsu, H
    Diaz, S
    Iber, J
    Nickerson, E
    Wright, KL
    Muchmore, EA
    Nelson, DL
    Warren, ST
    Varki, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) : 11751 - 11756
  • [8] Inactivation of CMP-N-acetylneuraminic acid hydroxylase occurred prior to brain expansion during human evolution
    Chou, HH
    Hayakawa, T
    Diaz, S
    Krings, M
    Indriati, E
    Leakey, M
    Paabo, S
    Satta, Y
    Takahata, N
    Varki, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (18) : 11736 - 11741
  • [9] Enhanced binding of the neural siglecs, myelin-associated glycoprotein and Schwann cell myelin protein, to Chol-1 (α-series) gangliosides and novel sulfated Chol-1 analogs
    Collins, BE
    Ito, H
    Sawada, N
    Ishida, H
    Kiso, M
    Schnaar, RL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (53) : 37637 - 37643
  • [10] Binding specificities of the sialoadhesin family of I-type lectins - Sialic acid linkage and substructure requirements for binding of myelin-associated glycoprotein, Schwann cell myelin protein, and sialoadhesin
    Collins, BE
    Kiso, M
    Hasegawa, A
    Tropak, MB
    Roder, JC
    Crocker, PR
    Schnaar, RL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) : 16889 - 16895