Literature DB >> 7989345

Cloning and expression of myelin-associated oligodendrocytic basic protein. A novel basic protein constituting the central nervous system myelin.

Y Yamamoto1, R Mizuno, T Nishimura, Y Ogawa, H Yoshikawa, H Fujimura, E Adachi, T Kishimoto, T Yanagihara, S Sakoda.   

Abstract

We have screened genes predominantly expressed in the rat spinal cord, and we report here cloning of the most abundant unknown gene. It is a novel member of the central nervous system (CNS) myelin-constituting proteins, myelin-associated oligodendrocytic basic protein (MOBP). MOBP is abundantly expressed specifically in oligodendrocytes at the mRNA level only next to myelin basic protein (MBP) and proteolipid protein. Two isoforms have been confirmed. One of them has proline-rich tandem repeats and has 84% homology with human counterpart in terms of predicted amino acid sequences. The cDNA-derived primary structure predicts a small, soluble, basic protein. The immunoelectron microscopy has shown that MOBP is expressed throughout compact myelin. All these characteristics are similar to MBP. One definite difference between MBP and MOBP is that MOBP is expressed exclusively in the CNS myelin. These findings suggest that MOBP shares some important functions with MBP in the CNS myelin such as myelin compaction.

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Year:  1994        PMID: 7989345

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  18 in total

Review 1.  Polarity development in oligodendrocytes: sorting and trafficking of myelin components.

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Review 2.  Mitochondrial dysfunction in schizophrenia: an evolutionary perspective.

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3.  The mouse gene (Mobp) encoding myelin-associated oligodendrocytic basic protein maps to distal chromosome 9.

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6.  Encephalitogenicity of myelin-associated oligodendrocytic basic protein and 2',3'-cyclic nucleotide 3'-phosphodiesterase for BALB/c and SJL mice.

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8.  Cross-sectional and longitudinal analysis of myelin-reactive T cells in patients with multiple sclerosis.

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9.  Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci.

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Journal:  Acta Neuropathol       Date:  2016-04-26       Impact factor: 17.088

10.  Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration.

Authors:  Xuebao Zhang; Clement Y Chow; Zarife Sahenk; Michael E Shy; Miriam H Meisler; Jun Li
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