Tu Shichun, Shin Yeonsook, Zago Wagner M, States Bradley A, Eroshkin Alexey, Lipton Stuart A, Tong Gary G, Nakanishi Nobuki
Center for Neuroscience and Aging, Burnham Institute for Medical Research, La Jolla, CA 92037, USA.
Neuron. 2007 Jul 5;55(1):69-85. doi: 10.1016/j.neuron.2007.06.021.
We have characterized a rodent-specific gene family designated alpha-takusan (meaning "many" in Japanese). We initially identified a member of the family whose expression is upregulated in mice lacking the NMDAR subunit NR3A. We then isolated cDNAs encoding 46 alpha-takusan variants from mouse brains. Most variants share an approximately 130 aa long sequence, which contains the previously identified domain of unknown function 622 (DUF622) and is predicted to form coiled-coil structures. Single-cell PCR analyses indicate that one neuron can express multiple alpha-takusan variants and particular variants may predominate in certain cell types. Forced expression in cultured hippocampal neurons of two variants, alpha1 or alpha2, which bind either directly or indirectly to PSD-95, leads to an increase in PSD-95 clustering, dendritic spine density, GluR1 surface expression, and AMPAR activity. Conversely, treating cultured neurons with RNAi targeting alpha-takusan variants resulted in the opposite phenotype. Hence, alpha-takusan represents a large gene family that regulates synaptic activity.
我们已经鉴定出一个啮齿动物特有的基因家族,命名为α-高山(在日语中意为“许多”)。我们最初鉴定出该家族的一个成员,其在缺乏NMDAR亚基NR3A的小鼠中表达上调。然后,我们从小鼠大脑中分离出编码46种α-高山变体的cDNA。大多数变体共享一个约130个氨基酸长的序列,该序列包含先前鉴定的未知功能域622(DUF622),并预测会形成卷曲螺旋结构。单细胞PCR分析表明,一个神经元可以表达多种α-高山变体,并且特定变体可能在某些细胞类型中占主导地位。在培养的海马神经元中强制表达两种与PSD-95直接或间接结合的变体α1或α2会导致PSD-95聚集、树突棘密度、GluR1表面表达和AMPA受体活性增加。相反,用靶向α-高山变体的RNAi处理培养的神经元会导致相反的表型。因此,α-高山代表一个调节突触活动的大型基因家族。