Novel O-Mannosyl Phosphorylation of Alpha-Dystroglycan is Required for Laminin Binding: Implications for Congenital Muscular Dystrophy

被引：0
|
作者：
Yoshida-Moriguchi, Takako [1 ]
Yu, Liping [1 ]
Schachter, Harry [2 ]
Wells, Lance [3 ]
Campbell, Kevin [1 ]
机构：
[1] Univ Iowa, Iowa City, IA USA
[2] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[3] Univ Georgia, Complex Carbohydrate Res Ctr, Athens, GA 30602 USA
来源：
GLYCOBIOLOGY | 2010年 / 20卷 / 11期
关键词：
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：
127
引用
收藏
页码：1489 / 1490
页数：2
相关论文
共 11 条
  • [1] Novel O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding: implications for congenital muscular dystrophy
    Moriguchi, T.
    Yu, L.
    Schachter, H.
    Wells, L.
    Campbell, K.
    [J]. NEUROMUSCULAR DISORDERS, 2010, 20 (9-10) : 597 - 597
  • [2] O-Mannosyl Phosphorylation of Alpha-Dystroglycan Is Required for Laminin Binding
    Yoshida-Moriguchi, Takako
    Yu, Liping
    Stalnaker, Stephanie H.
    Davis, Sarah
    Kunz, Stefan
    Madson, Michael
    Oldstone, Michael B. A.
    Schachter, Harry
    Wells, Lance
    Campbell, Kevin P.
    [J]. SCIENCE, 2010, 327 (5961) : 88 - 92
  • [3] Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin
    Chiba, A
    Matsumura, K
    Yamada, H
    Inazu, T
    Shimizu, T
    Kusunoki, S
    Kanazawa, I
    Kobata, A
    Endo, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (04) : 2156 - 2162
  • [4] Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression
    Hu, Huaiyu
    Li, Jing
    Zhang, Zhen
    Yu, Miao
    [J]. NEUROSCIENCE LETTERS, 2011, 489 (01) : 10 - 15
  • [5] Clinical and mutational spectrum of congenital muscular dystrophy with defective alpha-dystroglycan glycosylation in Korea
    Cho, A.
    Lim, B.
    Kim, M.
    Kim, K.
    Chae, J.
    [J]. NEUROMUSCULAR DISORDERS, 2016, 26 : S163 - S163
  • [6] Roles of Matriglycan and the Underlying M3 Glycan on Alpha-Dystroglycan in Congenital Muscular Dystrophy
    Wells, Lance
    [J]. GLYCOBIOLOGY, 2022, 32 (11) : 1045 - 1045
  • [7] Novel laminin alpha 2 mutations in congenital muscular dystrophy
    Mendell, JT
    Feng, B
    Sahenk, Z
    Marzluf, GA
    Amato, AA
    Mendell, JR
    [J]. NEUROLOGY, 1997, 48 (03) : 3135 - 3135
  • [8] A novel glycosyltransferase is mutated in a form of congenital muscular dystrophy with secondary laminin α2 deficiency and abnormal glycosylation of α-dystroglycan.
    Brockington, M
    Blake, DJ
    Prandini, P
    Brown, SC
    Torelli, S
    Benson, MA
    Ponting, CP
    Estournet, B
    Romero, N
    Voit, T
    Sewry, CA
    Guicheney, P
    Muntoni, F
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 229 - 229
  • [9] Alpha-dystroglycan binding peptide A2G80-modified stealth liposomes as a muscle-targeting carrier for Duchenne muscular dystrophy
    Sasaki, Eri
    Hayashi, Yoshihiro
    Kimura, Yuka
    Sashida, Sanae
    Hamano, Nobuhito
    Nirasawa, Kei
    Hamada, Keisuke
    Katagiri, Fumihiko
    Kikkawa, Yamato
    Sakai, Takaaki
    Yoshida, Akihiro
    Kawada, Masahiro
    Hirashima, Shin-ichi
    Miura, Tsuyoshi
    Endo-Takahashi, Yoko
    Nomizu, Motoyoshi
    Negishi, Yoichi
    [J]. JOURNAL OF CONTROLLED RELEASE, 2021, 329 : 1037 - 1045
  • [10] Localization of laminin chains in the human retina: Possible implications for congenital muscular dystrophy associated with alpha 2-chain of laminin deficiency
    Toti, P
    DeFelice, C
    Malandrini, A
    Megha, T
    Cardone, C
    Villanova, M
    [J]. NEUROMUSCULAR DISORDERS, 1997, 7 (01) : 21 - 25
12