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The expression patterns of deubiquitinating enzymes, USP22 and Usp22

机译:去泛素化酶USP22和Usp22的表达模式

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摘要

Deubiquitinating enzymes regulate a number of cellular mechanisms including pre-implantation, growth and differentiation, oncogenesis, cell cycle progression, transcriptional activation, and signal transduction. In this study, we have identified a novel human deubiquitinating enzyme gene, USP22, and its mouse homologue, Usp22. They encode 525 amino acids (approximate MW: 60kDa) and contains Cys, Asp (I), His and Asp/Asn (II), the highly conserved domains of the UBP family of deubiquitinating enzymes. The biochemical assay revealed that they have deubiquitinating enzyme activity. Northern blot analysis for USP22 showed moderate expression in various organs including human heart and skeletal muscle, and weak expression in lung and liver. However, Usp22 is expressed strongly in brain and weakly in other organs. We investigated the expression level of Usp22 mRNA and the localization during implantation and early pregnancy by in situ hybridization. Interestingly, Northern blot analysis showed the strong expression of Usp22 between embryonic days E10.5 and E12.5. Whole mount in situ hybridization staining revealed that Usp22 was expressed in the midbrain, forebrain, hindbrain and dorsal root ganglia of embryos at E12.5. Embryos at E12.5 showed the pronounced expression of Usp22 during the early embryonic development, although its expression was not detectable in the gut, liver and heart.
机译:去泛素化酶调节许多细胞机制,包括植入前,生长和分化,致癌作用,细胞周期进程,转录激活和信号转导。在这项研究中,我们确定了一个新的人类去泛素化酶基因USP22及其小鼠同源物Usp22。它们编码525个氨基酸(大约MW:60kDa),并包含Cys,Asp(I),His和Asp / Asn(II),这是UBP脱泛素化酶家族中高度保守的域。生化测定显示它们具有去泛素化酶活性。针对USP22的Northern印迹分析显示,在包括人的心脏和骨骼肌在内的各种器官中中等表达,而在肺和肝中则弱表达。但是,Usp22在大脑中强烈表达,而在其他器官中则弱表达。我们通过原位杂交研究了Usp22 mRNA的表达水平以及在植入和早期妊娠期间的定位。有趣的是,Northern印迹分析显示在胚胎第E10.5天和E12.5天之间Usp22的强表达。整个安装原位杂交染色显示,Usp22在E12.5的胚胎中脑,前脑,后脑和背根神经节中表达。尽管在肠道,肝脏和心脏中无法检测到,但在E12.5的胚胎在早期胚胎发育过程中显示了Usp22的明显表达。

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