Mouse UBPy (mUBPy) is an ubiquitin-specific protease which belongs to a family of deubiquitinating enzymes (DUBs) implicated in several cellular processes related to both cell growth and differentiation. Previously, Northern blot analysis revealed an important expression of mUBPy in the testis and brain. However, a more comprehensive map of mUBPy localization in the central nervous system (CNS) is still lacking. In this study, we mapped the distribution of mUBPy in the mouse brain using nonradioactive in situ hybridization and immunohistochemical techniques. In general, transcript and protein showed a similar and widespread distribution. In particular, mUBPy was strongly expressed in the hippocampal formation, septal region, ventral pallidum, preoptic nucleus, periventricular nucleus of hypothalamus, compact part of the substantia nigra, ventral tegmental area, cochlear nucleus and granular cell layer of cerebellum. A moderate expression of mUBPy was found in the amygdaloid complex, supraoptic nucleus, arcuate and ventromedial nuclei of hypothalamus, lateral hypothalamic area and lateral and reticular part of the substantia nigra. Double labelling with the mUBPy antiserum and antisera against specific cell markers showed that the enzyme is generally expressed in neurons and, in specific regions, also in oligodendrocytes. Moreover, by using antisera to TH and mUBPy we found that mUBPy is localized in dopaminergic neurons. The different distribution of mUBPy in the distinct regions of the brain suggests that it could be related to different deubiquitinating processes; in particular, in the areas where it is expressed at high levels, mUBPy could exert a specialized function through its interaction with specific protein substrates.
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http://dx.doi.org/10.1016/j.brainres.2007.12.014 | DOI Listing |
RSC Adv
February 2020
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University Katahira 2-1-1, Aoba-ku Sendai 980-8577 Japan +81-22-217-5587.
It has been difficult to selectively modify the surface of molecular crystals by chemical reactions because they usually have no reaction points on their surfaces. In this paper, focusing on the unique nanocrystal surface of the polymer metal complex (PMC) [{Cu(μ-Br)(PPh)}(μ-bpy)] having an exposed reactive terminal chain, we successfully modified the surface of PMC nanocrystals (NCs) through an alkylation reaction. Interestingly, after the alkylation reaction, the luminescence spectrum of PMC NCs blue-shifted, and the luminescence quantum yield increased.
View Article and Find Full Text PDFRSC Adv
May 2018
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University Katahira 2-1-1, Aoba-ku Sendai 980-8577 Japan.
We have successfully visualized the surface terminal structure of polymer-metal complex [{Cu(μ-Br)(PPh)}(μ-bpy)] nanocrystals (NCs) using Prussian blue (PB) nanoparticles (NPs). From TEM observation and analysis of the electron beam diffraction pattern, it was found that the (010) plane had grown well, and that the terminal ends of main chains would be located on the (010) plane of the present NCs as a dangling bond. Actually, PB NPs were selectively adsorbed on the (010) plane of [{Cu(μ-Br)(PPh)}(μ-bpy)] NCs.
View Article and Find Full Text PDFBrain Res
October 2010
Department of Biology, University of Genova, Genova, Italy.
Mouse UBPy (mUBPy) belongs to the family of ubiquitin-specific processing proteases (UBPs). In this study we have investigated the expression of mUBPy in the brain and sensory organs of mouse at different embryonic stages (E9, E11, E13, E15, E17, E19) and during the postnatal stages P0, P1, P2, P4 and P5 using Western blot and immunohistochemistry. mUBPy-immunoreactive cell bodies first appeared at stage E11 in several brain regions, particularly in the walls surrounding the vesicles and the ventricles.
View Article and Find Full Text PDFGen Comp Endocrinol
April 2010
Dipartimento di Medicina Sperimentale, Seconda Università di Napoli, Italy.
Mouse ubiquitin-specific processing protease (mUBPy) is a deubiquitinating enzyme highly expressed in both brain and testis. In testis, it interacts with the DnaJ protein, MSJ-1; both mUBPy and MSJ-1 are located on the cytoplasmic surface of the developing acrosome and in the centrosomal region during spemiogenesis. Present data show the first appearance in testis of mUbpy mRNA and protein at 10 days post-partum (d.
View Article and Find Full Text PDFBrain Res
February 2008
Department of Biology, University of Genova, V.le Benedetto XV, 5 16132 Genova, Italy.
Mouse UBPy (mUBPy) is an ubiquitin-specific protease which belongs to a family of deubiquitinating enzymes (DUBs) implicated in several cellular processes related to both cell growth and differentiation. Previously, Northern blot analysis revealed an important expression of mUBPy in the testis and brain. However, a more comprehensive map of mUBPy localization in the central nervous system (CNS) is still lacking.
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