4.2 Article

Biochemical and histochemical analysis of 71 kDa dystrophin isoform (Dp71f) in rat brain

Journal

ACTA HISTOCHEMICA
Volume 103, Issue 2, Pages 209-224

Publisher

ELSEVIER GMBH, URBAN & FISCHER VERLAG
DOI: 10.1078/0065-1281-00591

Keywords

Duchenne muscular dystrophy; dystrophin isoforms; rat brain; Dp71; cytoskeleton

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Dp71 is a member of the dystrophin family and the most abundant dmd gene product in the brain. In the present study, we focused on a short dystrophin transcript named Dp71f, which is alternatively spliced when exon 78 is absent The topographic localization of this protein in the encephalon has not been properly described yet, nor its cellular or subcellular localization, and even less its functions. Dp71f was found to be a cytoplasmic 70 kDa protein and localized in all encephalon regions studied. Double labeling using specific markers for various cell types confirmed Dp71f distribution in the cytoplasm of all cell types studied. Labeling was more conspicuous near the nucleus and diminished towards the periphery of cells. In some cases, we observed cells that were positive for actin and Dp71f in regions corresponding to lamellipodia-like structures. Dp71f and Dp71d isoforms were differently distributed. Our study is the first specific and unambiguous description of the topography and cellular localization patterns of Dp71f in brain, suggesting that Dp71f is a ubiquitous protein.

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