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Published on: June 25, 2019
Developmental expression of the collagen-binding heat-shock protein GP46 and collagen types I and IV in rat tissues
B J Pak1, D A Wigle, J D Watson
1Department of Anatomy and Cell Biology, Queen's University, Kingston, Canada.
Insights
The expression of glycoprotein gp46 and collagen mRNA changes during rat development. Gp46 regulation is tissue-specific, with complex links to collagen expression during ontogenesis.
Area of Science:
- Developmental biology
- Molecular biology
- Biochemistry
Background:
- Glycoprotein gp46 (collagen-binding heat-shock protein) plays a role in tissue development.
- Understanding the regulation of gp46 and its relationship with collagen during postnatal development is crucial for tissue ontogenesis.
Purpose of the Study:
- To determine the temporal expression of gp46 protein and mRNA in rat heart, kidney, and lung during postnatal development.
- To investigate the co-regulation of gp46 with collagen types I and IV mRNA during ontogenesis.
Main Methods:
- Western blot analysis was used to quantify gp46 protein levels.
- mRNA expression levels for gp46, collagen type I alpha 1(I), and collagen type IV alpha 1(IV) were examined.
- Analysis was performed on tissue samples from different postnatal developmental stages.
Main Results:
- Gp46 protein levels were developmentally regulated, showing high levels early postnatally and decreasing significantly by day 69 in heart and kidney.
- Gp46 mRNA expression did not consistently correlate with protein levels, suggesting complex regulation.
- The correlation between gp46 protein and collagen mRNA expression (types I and IV) was tissue-specific.
Conclusions:
- Gp46 is developmentally regulated at both protein and mRNA levels in a tissue-specific manner.
- The relationship between gp46 and collagen mRNA expression is also tissue-specific, indicating distinct regulatory mechanisms in different organs.
Abstract:
The temporal expression of protein and mRNA encoding the collagen-binding heat-shock glycoprotein, gp46, were determined in the heart, kidney, and lung during early rat postnatal development. The steady-state levels of collagen types I and IV mRNA expression were also examined to determine if gp46 and these collagen types are co-regulated during ontogenesis. Western blot analysis using a monoclonal antibody to gp46 revealed that gp46 levels are developmentally regulated. In heart and kidney, gp46 levels were high on days 3 and 8, reduced significantly on day 25, and low to undetectable on day 69. Protein levels of gp46 in the lung exhibited a similar temporal pattern except on day 3, when very low levels of gp46 were detected. mRNA expression of gp46 during early postnatal development did not correlate with gp46 protein accumulation in these tissues, suggesting a complex pre- and post-translational regulatory scheme. In the heart, protein levels of gp46 correlated well with collagen type I alpha 1(I) mRNA expression but not with collagen type IV alpha 1(IV). In contrast, gp46 protein levels closely paralleled alpha 1(IV) expression in the kidney. Gp46 levels exhibited no apparent correlation with either alpha 1(I) or alpha 1(IV) levels in the lung. These results show that gp46 is developmentally regulated at both the protein and mRNA levels in a tissue specific manner. The relationship between gp46 and collagen alpha 1(I) and alpha 1(IV) chain mRNA expression also has been shown to be tissue specific.
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