Hu Xu-Chu, Zhou Hong-Juan, Hu Feng-Yu, Ma Chang-Ling, Zhao Jun-Hong, Huang Can, Zheng Xiao-Ling, Xu Jin, Yu Xin-Bing
Department of Parasitology, Zhongshan College of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2009 Apr;27(2):95-101.
To illustrate the distribution of ATP synthase b subunit in the tissue of Clonorchis sinensis adult and its subcellular mimical localization in HeLa cells.
With the antiserum against recombinant CsATP-synt_B protein raised from SD rats as primary antibody, paraffin sections of the adult of C. sinensis were processed by the method of fluorescent immunohistochemistry to observe the distribution of CsATP-synt_B protein in adult worm. According to the prediction by bioinformatics of the definite mitochondrial targeting sequence (MTS) and probable Bipartite nuclear localization signals (NLS_BP)in CsATP-syntB sequence, recombinant pEGFP-N1 plasmids containing the intact and three defective CsATP-synt_B sequence with single defect of MTS or NLS_BP or double defect respectively were constructed. The recombinant plasmids and the control plasmid-pEGFP-N1, pEYFP-Mito and H2B-CFP, were transfected into the HeLa cells by Lipofectamine 2000 reagent and the subcellular location of the GFP fusion protein was observed with confocal microscopy.
The CsATP-synt_B protein appeared to distribute all over the adult worm, especially abundant on the acetabulum, ovary, vitellarium and tegument. The intact CsATP-synt_B was definitely expressed in mitochondria and/or nucleus of infected HeLa cells, whereas the MTS-deleted mutant only in cytoplasma and nucleus, the NLS_BP-deleted mutant in mitochondria and cytoplasm, and the double defect mutant only in cytoplasm.
The distribution of CsATP-synt_B in adult is accord with that of mitochondria, and mainly exits in the organs and the tissues of active energy metabolism. This study first predicted and confirmed that CsATP-synt_B can be expressed in the nucleus.
阐明ATP合酶β亚基在中国华支睾吸虫成虫组织中的分布及其在HeLa细胞中的亚细胞模拟定位。
以从SD大鼠体内获得的抗重组CsATP-synt_B蛋白的抗血清为一抗,采用荧光免疫组织化学方法处理华支睾吸虫成虫石蜡切片,观察CsATP-synt_B蛋白在成虫中的分布。根据生物信息学预测CsATP-syntB序列中确定的线粒体靶向序列(MTS)和可能的双分型核定位信号(NLS_BP),构建分别含有完整的和三种有缺陷的CsATP-synt_B序列的重组pEGFP-N1质粒,这些缺陷分别为MTS单缺陷、NLS_BP单缺陷或双缺陷。将重组质粒以及对照质粒-pEGFP-N1、pEYFP-Mito和H2B-CFP,用Lipofectamine 2000试剂转染HeLa细胞,并用共聚焦显微镜观察GFP融合蛋白的亚细胞定位。
CsATP-synt_B蛋白似乎分布于整个成虫虫体,尤其在吸盘、卵巢、卵黄腺和体表丰富。完整的CsATP-synt_B在感染的HeLa细胞的线粒体和/或细胞核中明确表达,而缺失MTS的突变体仅在细胞质和细胞核中表达,缺失NLS_BP的突变体在线粒体和细胞质中表达,双缺陷突变体仅在细胞质中表达。
CsATP-synt_B在成虫中的分布与线粒体的分布一致,主要存在于活跃能量代谢的器官和组织中。本研究首次预测并证实CsATP-synt_B可在细胞核中表达。