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分泌颗粒标记蛋白嗜铬粒蛋白B在细胞核中的定位。在转录调控中的潜在作用。

Localization of the secretory granule marker protein chromogranin B in the nucleus. Potential role in transcription control.

作者信息

Yoo Seung Hyun, You Soon Hee, Kang Moon Kyung, Huh Yang Hoon, Lee Choong Sik, Shim Chan Seob

机构信息

National Creative Research Initiative Center for Secretory Granule Research, Korea Advanced Institute of Science and Technology, Yu Sung Gu, Dae Jeon, Korea 305-701.

出版信息

J Biol Chem. 2002 May 3;277(18):16011-21. doi: 10.1074/jbc.M105594200. Epub 2002 Feb 19.

Abstract

Chromogranins A (CGA) and B (CGB) are two major Ca(2+) storage proteins of the secretory granules of neuroendocrine cells. Nevertheless, we found in the present study that CGB was also localized in the nucleus. In immunogold electron microscopy using bovine adrenal medullary chromaffin cells, it was found that the number of CGB-labeled gold particles localized per microm(2) of the nucleus was equivalent to 20% that of CGB-labeled gold particles localized per microm(2) of the secretory granules. Considering that CGB is estimated to exist in the 0.1-0.2-mm range in the secretory granules of bovine chromaffin cells, 20% of these amounts to 20-40 microm. In addition, transfection of CGA and CGB into nonneuroendocrine COS-7 and NIH3T3 cells repeatedly indicated the nuclear localization of CGB in addition to its usual localization in the cytoplasm. Moreover, immunoblot and immunogold electron microscopy analyses of neuroendocrine PC12 cells also showed the existence of endogenous CGB in both the cytosol and the nucleus. Nuclear routing of CGB did not appear to depend entirely upon the nuclear localization signal as some of the nuclear localization signal mutant CGB were still targeted to the nucleus. In gene array assay, CGB was shown to either induce or suppress transcription of many genes including those of transcription factors. Of these we have analyzed eight genes, four induced (zinc finger protein, MEF2C, hCRP2, abLIM) and four suppressed (hcKrox, T3-receptor, troponin C, integrin) using the quantitative reverse transcription-PCR method and spectrophotometry to determine the transcription levels of each mRNA. CGB was shown to increase the transcription of zinc finger protein, MEF2C, hCRP2, and abLIM by 2.5-5-fold while suppressing that of hcKrox, T3-receptor, troponin C, and integrin by 60-75%. Given that MEF2C and hcKrox genes are transcription factors, these results pointed to the transcription control role of CGB in the nucleus.

摘要

嗜铬粒蛋白A(CGA)和嗜铬粒蛋白B(CGB)是神经内分泌细胞分泌颗粒中的两种主要钙储存蛋白。然而,我们在本研究中发现CGB也定位于细胞核中。在使用牛肾上腺髓质嗜铬细胞进行的免疫金电子显微镜研究中,发现每平方微米细胞核中CGB标记的金颗粒数量相当于每平方微米分泌颗粒中CGB标记的金颗粒数量的20%。考虑到据估计牛嗜铬细胞分泌颗粒中CGB的存在范围为0.1 - 0.2毫米,其中20%相当于20 - 40微米。此外,将CGA和CGB转染到非神经内分泌的COS - 7和NIH3T3细胞中,反复表明CGB除了通常定位于细胞质中外,还定位于细胞核。此外,对神经内分泌PC12细胞的免疫印迹和免疫金电子显微镜分析也显示,在细胞质和细胞核中均存在内源性CGB。CGB的核转运似乎并不完全依赖于核定位信号,因为一些核定位信号突变的CGB仍然靶向细胞核。在基因芯片分析中,CGB被证明可以诱导或抑制许多基因的转录,包括转录因子的基因。其中,我们使用定量逆转录 - PCR方法和分光光度法分析了八个基因,四个被诱导(锌指蛋白、MEF2C、hCRP2、abLIM),四个被抑制(hcKrox、T3受体、肌钙蛋白C、整合素),以确定每个mRNA的转录水平。结果显示,CGB可使锌指蛋白、MEF2C、hCRP2和abLIM的转录增加2.5 - 5倍,同时使hcKrox、T3受体、肌钙蛋白C和整合素的转录抑制60 - 75%。鉴于MEF2C和hcKrox基因是转录因子,这些结果表明CGB在细胞核中具有转录调控作用。

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