Motodate Rika, Saito Yuhki, Hata Saori, Suzuki Toshiharu
Laboratory of Neuroscience, Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita 12-Nishi 6, Kita-ku, Sapporo 060-0812, Japan.
Laboratory of Neuroscience, Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita 12-Nishi 6, Kita-ku, Sapporo 060-0812, Japan.
Brain Res. 2016 Sep 1;1646:227-234. doi: 10.1016/j.brainres.2016.05.054. Epub 2016 Jun 4.
The X11/Mint family of proteins comprises X11/X11α/Mint1, X11L/X11β/Mint2, and X11L2/X11γ/Mint3. Each of these molecules is an adaptor protein that contains a phosphotyrosine interaction/binding (PI/PTB) and two PDZ domains in its carboxy-terminal region. X11/Mint family members associate with a broad spectrum of membrane proteins, including Alzheimer's β-amyloid precursor protein (APP), alcadeins, and low density lipoprotein receptor proteins, as well as various cytoplasmic proteins including Arf, kalirin-7, and Munc18. In particular, X11 and X11L are thought to play various roles in the regulation of neural functions in brain. Nevertheless, the protein levels and respective localization of individual family members remain controversial. We analyzed the protein levels of X11 and X11L in the corresponding single- and double-knockout mice. X11 and X11L did not exhibit obvious changes of their protein levels when the other was absent, especially in cerebrum in which they were widely co-expressed. In cerebellum, X11 and X11L localized in characteristic patterns in various types of neurons, and X11 protein level increased without an obvious ectopic localization in X11L-knockout mice. Interestingly, only X11L protein existed specifically in brain, whereas, contrary to the accepted view, X11 protein was detected at the highest levels in brain but was also strongly detected in pancreas, testis, and paranephros. Together, our results indicate that both X11 and X11L exert largely in brain neurons, but X11 may also function in peripheral tissues.
X11/Mint蛋白家族由X11/X11α/Mint1、X11L/X11β/Mint2和X11L2/X11γ/Mint3组成。这些分子中的每一个都是衔接蛋白,在其羧基末端区域含有一个磷酸酪氨酸相互作用/结合(PI/PTB)结构域和两个PDZ结构域。X11/Mint家族成员与多种膜蛋白相关联,包括阿尔茨海默病β-淀粉样前体蛋白(APP)、阿尔卡德蛋白和低密度脂蛋白受体蛋白,以及包括Arf、卡利林-7和Munc18在内的各种细胞质蛋白。特别是,X11和X11L被认为在大脑神经功能的调节中发挥着多种作用。然而,各个家族成员的蛋白水平和各自的定位仍存在争议。我们分析了相应的单基因敲除和双基因敲除小鼠中X11和X11L的蛋白水平。当另一个缺失时,X11和X11L的蛋白水平没有表现出明显变化,尤其是在它们广泛共表达的大脑中。在小脑中,X11和X11L以特征性模式定位于各种类型的神经元中,并且在X11L基因敲除小鼠中,X11蛋白水平升高且没有明显的异位定位。有趣的是,只有X11L蛋白特异性存在于大脑中,而与普遍观点相反,X11蛋白在大脑中的水平最高,但在胰腺、睾丸和肾旁组织中也被大量检测到。总之,我们的结果表明,X11和X11L在很大程度上都在脑神经元中发挥作用,但X11也可能在外周组织中发挥功能。