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NE-dlg的克隆与特性分析:果蝇盘大(dlg)肿瘤抑制蛋白的一种新型人类同源物与APC蛋白相互作用。

Cloning and characterization of NE-dlg: a novel human homolog of the Drosophila discs large (dlg) tumor suppressor protein interacts with the APC protein.

作者信息

Makino K, Kuwahara H, Masuko N, Nishiyama Y, Morisaki T, Sasaki J, Nakao M, Kuwano A, Nakata M, Ushio Y, Saya H

机构信息

Department of Tumor Genetics and Biology, Kumamoto University School of Medicine, Honjo Kumamoto, Japan.

出版信息

Oncogene. 1997 May 22;14(20):2425-33. doi: 10.1038/sj.onc.1201087.

Abstract

We have cloned a cDNA for a novel human homolog of the Drosophila discs large (dig) tumor suppressor protein, termed NE-dlg (neuronal and endocrine dig). Northern blot analysis revealed that the gene is highly expressed in neuronal and endocrine tissues. Fluorescence in situ hybridization (FISH) and radiation hybrid mapping studies localized the NE-dlg gene to chromosome Xq13. We also found that the NE-dlg gene encoded a 100 kDa protein. Immunolocalization studies using an NE-dlg antibody showed that the protein tended to be expressed in non-proliferating cells, such as neurons, cells in Langerhans islets of the pancreas, myocytes of the heart muscles, and the prickle and functional layer cells of the esophageal epithelium. Proliferative cells, including various cultured cancer cell lines and basal cells in the esophageal epithelium, showed little expression of the NE-dlg protein. In addition, yeast two-hybrid screening and in vitro binding assays revealed that the NE-dlg interacted with the carboxyl-terminal region of the APC tumor suppressor protein. These data suggest that NE-dlg negatively regulates cell proliferation through its interaction with the APC protein.

摘要

我们克隆了一种与果蝇盘状大肿瘤抑制蛋白(dig)的新型人类同源物的cDNA,命名为NE-dlg(神经元和内分泌dig)。Northern印迹分析表明,该基因在神经元和内分泌组织中高度表达。荧光原位杂交(FISH)和辐射杂种图谱研究将NE-dlg基因定位到Xq13染色体。我们还发现NE-dlg基因编码一种100 kDa的蛋白质。使用NE-dlg抗体的免疫定位研究表明,该蛋白倾向于在非增殖细胞中表达,如神经元、胰腺胰岛细胞、心肌细胞以及食管上皮的棘层和功能层细胞。包括各种培养的癌细胞系和食管上皮基底细胞在内的增殖细胞,NE-dlg蛋白表达很少。此外,酵母双杂交筛选和体外结合试验表明,NE-dlg与APC肿瘤抑制蛋白的羧基末端区域相互作用。这些数据表明,NE-dlg通过与APC蛋白相互作用负向调节细胞增殖。

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