Charych Erik I, Li Rongwen, Serwanski David R, Li Xuejing, Miralles Celia P, Pinal Noelia, De Blas Angel L
Department of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut 06269-3156, USA.
J Neurochem. 2006 May;97(3):884-98. doi: 10.1111/j.1471-4159.2006.03795.x. Epub 2006 Mar 15.
We cloned two novel alternatively-spliced mRNA isoforms of glutamate receptor interacting protein 1 (GRIP1) which we named GRIP1d and GRIP1e 4-7. GRIP1d is a 135 kDa, 7-PDZ-domain variant of GRIP1, containing the 12 amino acid C-terminus originally described for the 4-PDZ-domain GRIP1c 4-7. GRIP1e 4-7 is a 75 kDa 4-PDZ-domain variant of GRIP1, containing the 12 amino acid C-terminus originally described for the 7-PDZ-domain GRIP1a/b. Northern blots indicated that GRIP1d mRNA is 5.1 kb long and abundant in brain. An antibody to the C-terminus of the 75 kDa GRIP1c 4-7 also recognized an abundant 135 kDa protein, consistent with the predicted size of GRIP1d. Similarly, an antibody to the C-terminus of the 135 kDa GRIP1a/b also recognized a low abundance 75 kDa protein, consistent with the predicted size of GRIP1e 4-7. Immunocytochemistry of hippocampal cultures and intact brain using these antibodies showed that (i) these isoforms are present in both GABAergic and glutamatergic synapses, and (ii) the isoforms co-localize in individual synapses. While GRIP1a/b isoforms are abundant in interneurons and highly concentrated in GABAergic presynaptic terminals, the isoforms recognized by the antibody to the C-terminus common to GRIP1c 4-7 and GRIP1d are much less abundant in interneurons and preferentially concentrate at the postsynaptic complex.
我们克隆了谷氨酸受体相互作用蛋白1(GRIP1)的两种新的可变剪接mRNA异构体,分别命名为GRIP1d和GRIP1e 4 - 7。GRIP1d是一种135 kDa、具有7个PDZ结构域的GRIP1变体,包含最初在具有4个PDZ结构域的GRIP1c 4 - 7中描述的12个氨基酸的C末端。GRIP1e 4 - 7是一种75 kDa、具有4个PDZ结构域的GRIP1变体,包含最初在具有7个PDZ结构域的GRIP1a/b中描述的12个氨基酸的C末端。Northern印迹表明,GRIP1d mRNA长5.1 kb,在脑中含量丰富。针对75 kDa的GRIP1c 4 - 7的C末端的抗体也识别出一种丰富的135 kDa蛋白质,这与GRIP1d的预测大小一致。同样,针对135 kDa的GRIP1a/b的C末端的抗体也识别出一种低丰度的75 kDa蛋白质,这与GRIP1e 4 - 7的预测大小一致。使用这些抗体对海马培养物和完整大脑进行免疫细胞化学分析表明:(i)这些异构体存在于GABA能和谷氨酸能突触中,并且(ii)这些异构体在单个突触中共定位。虽然GRIP1a/b异构体在中间神经元中丰富且高度集中在GABA能突触前终末,但针对GRIP1c 4 - 7和GRIP1d共有的C末端的抗体识别的异构体在中间神经元中的丰度要低得多,并且优先集中在突触后复合体。