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Regional expression of myelin protein genes in the developing mouse brain: in situ hybridization studies
1Mental Retardation Research Center, UCLA School of Medicine 90024.
Abstract:
Expression of mRNAs for the two major myelin proteins, myelin basic protein (MBP) and proteolipid protein (PLP), was examined in a number of regions of the developing mouse brain using in situ hybridization. In general, MBP and PLP mRNAs were observed to be coexpressed during ontogeny, prior to the histological appearance of myelin. Expression of both mRNAs was detected as early as 6 hours postpartum in the medulla oblongata and, with development, expression of these mRNAs progressed in a caudal to rostral direction. Peak expression occurred at approximately postnatal day 20 in most regions examined, regardless of time of onset of expression. As myelination proceeded, two different labeling patterns were observed with the PLP and MBP 35S-labeled cDNA probes. In the earliest stages of myelinogenesis MBP mRNA labeling was restricted to oligodendrocyte cell bodies, but shortly after the gene began to be expressed the labeling became more diffuse. In contrast, PLP mRNA labeling remained over or surrounding oligodendrocyte cell bodies at all stages of myelinogenesis. These two distinctly different patterns of labeling are consistent with alternative intracellular trafficking of MBP and PLP mRNAs, in which PLP mRNAs remain associated with ribosomes within the cell soma and MBP mRNAs move from the cell soma to the oligodendrocyte processes at a specific stage early in myelinogenesis. However, there appeared to be a clear time lag between the onset of MBP mRNA expression and the movement of ribosomes carrying MBP mRNAs into the oligodendrocyte processes. Additionally, the in situ hybridization studies revealed a population of unidentified cells residing in cortical molecular layers that express PLP mRNA in the absence of MBP mRNA.
Insights
Myelin basic protein (MBP) and proteolipid protein (PLP) mRNAs are coexpressed in the developing mouse brain before myelin appears. Distinct trafficking patterns suggest differential intracellular transport of these key myelin protein mRNAs.
Area of Science:
- Neuroscience
- Molecular Biology
- Developmental Biology
Background:
- Myelin is crucial for rapid nerve impulse transmission in the central nervous system.
- Myelin basic protein (MBP) and proteolipid protein (PLP) are the major structural proteins of myelin.
- Understanding the spatiotemporal expression and trafficking of their mRNAs is key to deciphering myelin formation.
Purpose of the Study:
- To investigate the expression patterns of MBP and PLP mRNAs during mouse brain development.
- To elucidate the intracellular localization and trafficking of MBP and PLP mRNAs.
- To identify potential differences in mRNA regulation during myelinogenesis.
Main Methods:
- In situ hybridization using 35S-labeled cDNA probes for MBP and PLP.
- Analysis of mRNA expression in various regions of the developing mouse brain.
- Correlation of mRNA expression with histological stages of myelination.
Main Results:
- MBP and PLP mRNAs are coexpressed early in development, preceding myelin formation.
- mRNA expression progresses in a caudal-to-rostral direction, peaking around postnatal day 20.
- Distinct labeling patterns indicate MBP mRNA moves to oligodendrocyte processes, while PLP mRNA remains in the cell soma.
- A time lag exists between MBP mRNA onset and its translocation to processes.
- Unidentified cells in cortical layers express PLP mRNA without MBP mRNA.
Conclusions:
- MBP and PLP mRNAs exhibit coordinated but distinct spatiotemporal expression during mouse brain development.
- Differential intracellular trafficking mechanisms exist for MBP and PLP mRNAs.
- These findings provide insights into the regulation of myelin protein synthesis during myelinogenesis.