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大鼠脑中GRIP1两种新型剪接形式的鉴定与表征

Identification and characterization of two novel splice forms of GRIP1 in the rat brain.

作者信息

Charych Erik I, Li Rongwen, Serwanski David R, Li Xuejing, Miralles Celia P, Pinal Noelia, De Blas Angel L

机构信息

Department of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut 06269-3156, USA.

出版信息

J Neurochem. 2006 May;97(3):884-98. doi: 10.1111/j.1471-4159.2006.03795.x. Epub 2006 Mar 15.

Abstract

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.

摘要

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。

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