Literature DB >> 1717701

Spatial distribution of myelin basic protein mRNA and polypeptide in quaking oligodendrocytes in culture.

E Barbarese1.   

Abstract

In the CNS, myelin is formed from the expansion of oligodendrocyte processes. In order to study myelin assembly in the hypomyelinating mutant mouse quaking (qk), cultures of oligodendrocytes were established from affected and control animals. The cytoarchitecture of the oligodendrocytes was analyzed by performing morphometric measurements after immunostaining with antitubulin. The results indicate that the gross morphology of the processes is similar in control and mutant cells. The localization of the message for the myelin structural component, myelin basic protein (MBP), was examined by in situ hybridization. In control oligodendrocytes, 80% of MBP mRNA is found in the processes. In contrast, only 23% of MBP mRNA is localized to these structures in the mutant; the majority of MBP mRNA remains in the cell body. The mutant cells are capable of distributing mRNAs to the periphery as shown by the presence of tubulin mRNA in their processes. MBP polypeptide was visualized by immunofluorescence and found in the perikaryon, processes and membranous expansions of the control cells. In the mutant, it is largely confined to the perikaryon, reflecting the distribution of the mRNA. These results suggest that the localization of MBP polypeptide is achieved by restricting the distribution of its mRNA, and that MBP assembly into the myelin membrane occurs in the processes. This step appears to be blocked in qk oligodendrocytes in culture.

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Year:  1991        PMID: 1717701     DOI: 10.1002/jnr.490290302

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  11 in total

1.  Tyrosine phosphorylation of QKI mediates developmental signals to regulate mRNA metabolism.

Authors:  Youyi Zhang; Zifan Lu; Li Ku; Yuntao Chen; Houping Wang; Yue Feng
Journal:  EMBO J       Date:  2003-04-15       Impact factor: 11.598

2.  Glial-cell cultures from brains of carbonic anhydrase II-deficient mutant mice: delay in oligodendrocyte maturation.

Authors:  W Cammer
Journal:  Neurochem Res       Date:  1998-03       Impact factor: 3.996

3.  Functional implications for the microtubule-associated protein tau: localization in oligodendrocytes.

Authors:  P LoPresti; S Szuchet; S C Papasozomenos; R P Zinkowski; L I Binder
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-24       Impact factor: 11.205

4.  A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination.

Authors:  Janice K Noveroske; Rebecca Hardy; Jason D Dapper; Hannes Vogel; Monica J Justice
Journal:  Mamm Genome       Date:  2005-10-20       Impact factor: 2.957

5.  Neural cell type-specific expression of QKI proteins is altered in quakingviable mutant mice.

Authors:  R J Hardy; C L Loushin; V L Friedrich; Q Chen; T A Ebersole; R A Lazzarini; K Artzt
Journal:  J Neurosci       Date:  1996-12-15       Impact factor: 6.167

6.  Destabilization and mislocalization of myelin basic protein mRNAs in quaking dysmyelination lacking the QKI RNA-binding proteins.

Authors:  Z Li; Y Zhang; D Li; Y Feng
Journal:  J Neurosci       Date:  2000-07-01       Impact factor: 6.167

7.  Specificity of the STAR/GSG domain protein Qk1: implications for the regulation of myelination.

Authors:  Sean P Ryder; James R Williamson
Journal:  RNA       Date:  2004-07-23       Impact factor: 4.942

8.  Structure-function analysis of Qk1: a lethal point mutation in mouse quaking prevents homodimerization.

Authors:  T Chen; S Richard
Journal:  Mol Cell Biol       Date:  1998-08       Impact factor: 4.272

9.  Essential function, sophisticated regulation and pathological impact of the selective RNA-binding protein QKI in CNS myelin development.

Authors:  Katrina Bockbrader; Yue Feng
Journal:  Future Neurol       Date:  2008-11

10.  Transport and localization elements in myelin basic protein mRNA.

Authors:  K Ainger; D Avossa; A S Diana; C Barry; E Barbarese; J H Carson
Journal:  J Cell Biol       Date:  1997-09-08       Impact factor: 10.539

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