Characterization and immunolocalization of mutated ornithine decarboxylase antizyme from Angiostrongylus cantonensis

被引:1
作者
Chen, Jing [1 ,2 ]
Liu, Qian [1 ,2 ]
Yang, Xiao [1 ,2 ]
Wu, Xiansheng [1 ,2 ]
Zhang, Dongjing [1 ,2 ]
He, Ai [1 ,2 ]
Zhan, Ximei [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Parasitol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Minist Educ, Key Lab Trop Dis Control, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Angiostrongylus cantonensis; Mutated ornithine decarboxylase antizyme; Clone; Cell proliferation; CELL-GROWTH; MOLECULAR CHARACTERIZATION; EXPRESSION; POLYAMINES; INHIBITOR; CARCINOGENESIS; PROLIFERATION; CONSERVATION; INDUCTION; TARGETS;
D O I
10.1016/j.molbiopara.2013.06.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ornithine decarboxylase antizyme (OAZ), a prominent regulator of cell proliferation, DNA/RNA transformation and tumorigenesis, can bind to ornithine decarboxylase (ODC) and facilitate its degradation. Expression of OAZ requires a unique ribosomal frame shift that is regulated by levels of polyamine in the cell. In this study, we cloned an OAZ gene with the +1 ribosomal frame-shift from a fourth-stage larvae cDNA library of Angiostrongylus cantonensis. We removed one nucleotide to express the gene without polyamine. The sequence analysis showed that the deleted-mutation ornithine decarboxylase antizyme (DM-AcOAZ) contained a conservative domain related to other species OAZ. Quantitative real-time PCR revealed that DM-AcOAZ was expressed in L3 and L4 stages and adult female worms. More notably the expression level is the highest in the adult female stage. Immunohistochemical studies indicated that DM-AcOAZ was specifically localized in the uterus, oocyte and intestine in adult female worms. MTT assays showed that in DM-AcOAZ transfected HeLa cells, cell proliferation is inhibited. In conclusion, DM-AcOAZ may be a female-enriched protein and may involved in the cell proliferation in A. cantonensis. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:76 / 81
页数:6
相关论文
共 26 条
[1]   SPERMINE TOXICITY AND GLUTATHIONE DEPLETION IN BHK-21/C13 CELLS [J].
BRUNTON, VG ;
GRANT, MH ;
WALLACE, HM .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (08) :1893-1900
[2]  
Chen Feng, 2011, Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi, V23, P687
[3]   Stable siRNA-mediated silencing of antizyme inhibitor: regulation of ornithine decarboxylase activity [J].
Choi, KS ;
Suh, YH ;
Kim, WH ;
Lee, TH ;
Jung, MH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 328 (01) :206-212
[4]  
Deng ZH, 2011, SE ASIAN J TROP MED, V42, P1047
[5]  
Feith DJ, 2001, CANCER RES, V61, P6073
[6]  
Fong LYY, 2003, CANCER RES, V63, P3945
[7]   Polyamines and cancer: Old molecules, new understanding [J].
Gerner, EW ;
Meyskens, FL .
NATURE REVIEWS CANCER, 2004, 4 (10) :781-792
[8]   Preliminary molecular characterization of the human pathogen Angiostrongylus cantonensis [J].
He, Hualiang ;
Cheng, Mei ;
Yang, Xiao ;
Meng, Jinxiu ;
He, Ai ;
Zheng, Xiaoying ;
Li, Zhuoya ;
Guo, Pengjuan ;
Pan, Zhihua ;
Zhan, Ximei .
BMC MOLECULAR BIOLOGY, 2009, 10 :97
[9]   Alterations in the expression level of a putative aspartic protease in the development of Angiostrongylus cantonensis [J].
Hwang, Kao-Pin ;
Chang, Shih-Hsin ;
Wang, Lian-Chen .
ACTA TROPICA, 2010, 113 (03) :289-294
[10]   Conservation of polyamine regulation by translational frameshifting from yeast to mammals [J].
Ivanov, IP ;
Matsufuji, S ;
Murakami, Y ;
Gesteland, RF ;
Atkins, JF .
EMBO JOURNAL, 2000, 19 (08) :1907-1917