Molecular cloning of a peroxidase gene from poplar and its expression in response to stress

被引:15
作者
Bae, Eun-Kyung [1 ]
Lee, Hyoshin
Lee, Jae-Soon
Noh, Eun-Woon
Jo, Jinki
机构
[1] Korea Forest Res Inst, Div Biotechnol, Suwon 441350, South Korea
[2] Kyungpook Natl Univ, Dept Anim Sci & Biotechnol, Taegu 702701, South Korea
关键词
bacterial-elicitor oxidative stress; peroxidase; poplar suspension cell; wounding;
D O I
10.1093/treephys/26.11.1405
中图分类号
S7 [林业];
学科分类号
0829 ; 0907 ;
摘要
To elucidate the precise functions of peroxidase in poplar (Populus alba x P. tremula var. glandulosa), we cloned a peroxidase gene (PoPOD1) from poplar suspension culture cells and examined its expression pattern in response to various stresses. PoPOD1 showed the highest homology with a bacterial-induced peroxidase gene from cotton (Gossypium hirsutum L.). The PoPOD1 gene encodes a putative 316 amino acid protein with an N-terminal signal peptide of 23 residues. The DNA blot analysis indicated that PoPOD1 is a single copy gene in the poplar genome. The RNA blot analyses indicated that PoPOD1 shows cell-culture-specific expression. Expression of PoPOD1 is down-regulated by various treatments including treatment with some metals, NaCl, methyl viologen and polyethylene glycol, and by the plant growth regulators, jasmonic acid (JA) and gibberellic acid (GA(3)). The gene is significantly up-regulated by the bacterial-elicitor laminarin and by wounding. Thus, PoPOD1 gene expression is sensitively and specifically regulated at the transcription level. Because both JA and GA3 appear to be involved in the regulation of PoPOD1 expression in poplar cells, we postulate that the peroxidase encoded by PoPOD1 plays a pivotal role in defense against pathogen invasion, possibly through the formation of a cell wall barrier over the wound.
引用
收藏
页码:1405 / 1412
页数:8
相关论文
共 41 条
[1]   Cloning and characterization of a jasmonate inducible rice (Oryza sativa L.) peroxidase gene, OsPOX, against global signaling molecules and certain inhibitors of kinase-signaling cascade(s) [J].
Agrawal, GK ;
Rakwal, R ;
Jwa, NS .
PLANT SCIENCE, 2002, 162 (01) :49-58
[2]  
ASSCHE FV, 1988, ENVIRON POLLUT, V52, P103
[3]   Validating internal controls for quantitative plant gene expression studies [J].
Brunner A.M. ;
Yakovlev I.A. ;
Strauss S.H. .
BMC Plant Biology, 4 (1)
[4]   Oxidative burst and hypoosmotic stress in tobacco cell suspensions [J].
Cazalé, AC ;
Rouet-Mayer, MA ;
Barbier-Brygoo, H ;
Mathieu, Y ;
Laurière, C .
PLANT PHYSIOLOGY, 1998, 116 (02) :659-669
[5]   Effects of cadmium and copper on antioxidant capacities, lignification and auxin degradation in leaves of pea (Pisum sativum L.) seedlings [J].
Chaoui, A ;
El Ferjani, E .
COMPTES RENDUS BIOLOGIES, 2005, 328 (01) :23-31
[6]   Effects of cadmium and copper on peroxidase, NADH oxidase and IAA oxidase activities in cell wall, soluble and microsomal membrane fractions of pea roots [J].
Chaoui, A ;
Jarrar, B ;
El Ferjani, E .
JOURNAL OF PLANT PHYSIOLOGY, 2004, 161 (11) :1225-1234
[7]   Hydroxyl-radical production in physiological reactions - A novel function of peroxidase [J].
Chen, SX ;
Schopfer, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 260 (03) :726-735
[8]  
CHOI YI, 2001, J PLANT BIOTECHNOL, V3, P83
[9]   EARLY EVENTS IN THE ACTIVATION OF PLANT DEFENSE RESPONSES [J].
DIXON, RA ;
HARRISON, MJ ;
LAMB, CJ .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 1994, 32 :479-501
[10]   Responses of antioxidants to paraquat in pea leaves [J].
Donahue, JL ;
Okpodu, CM ;
Cramer, CL ;
Grabau, EA ;
Alscher, RG .
PLANT PHYSIOLOGY, 1997, 113 (01) :249-257