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玉米两个病程相关蛋白 10 基因的表达和功能特征。

Expression and functional characterization of two pathogenesis-related protein 10 genes from Zea mays.

机构信息

Department of Plant Pathology and Crop Physiology, 302 Life Sciences Building, Louisiana State University Agricultural Center, Baton Rouge, LA 70803, USA.

出版信息

J Plant Physiol. 2010 Jan 15;167(2):121-30. doi: 10.1016/j.jplph.2009.07.004.

Abstract

A novel PR10 gene (ZmPR10.1) was isolated from maize and its expression and function were compared with the previous ZmPR10. ZmPR10.1 shares 89.8% and 85.7% identity to ZmPR10 at the nucleotide and amino acid sequence level, respectively. ZmPR10 and ZmPR10.1 were mainly expressed in root tissue with low expression in other tissues. ZmPR10.1 had significantly lower expression than ZmPR10 in all tissues examined. The expression of both ZmPR10 and ZmPR10.1 was induced by most abiotic stresses including SA, CuCl(2), H(2)O(2), coldness, darkness and wounding during the 16-h treatments, and biotic stresses such as Erwinia stewartii and Aspergillus flavus infection. However, ZmPR10.1 was induced only 2 HAT and down-regulated thereafter, whereas ZmPR10 remained induced during the 16-h NAA treatment. Also, inoculation with Erwinia chrysanthemi caused about 2-fold induction in ZmPR10.1 expression 60 HAT but not significant changes for ZmPR10. Both ZmPR10.1 and ZmPR10 showed RNase activity in vitro with an optimal pH and temperature of 6.5 and 55 degrees C. Their RNase activities were significantly inhibited by low concentrations (1.0mM) of Cu(2+), Ag(+), Co(2+), SDS, EDTA or DTT. However, ZmPR10.1 possessed significantly higher (8-fold) specific RNase activity than ZmPR10. Also, ZmPR10.1 showed a stronger inhibition against bacterium Pseudomonas syringae pv. tomato DC3000 in vivo and fungus A. flavus in vitro than ZmPR10, indicating that ZmPR10.1 may also play an important role in host plant defense.

摘要

从玉米中分离出一个新的 PR10 基因(ZmPR10.1),并比较了其表达和功能与之前的ZmPR10 的异同。ZmPR10.1 在核苷酸和氨基酸序列水平上与ZmPR10 的同源性分别为 89.8%和 85.7%。ZmPR10 和 ZmPR10.1 主要在根组织中表达,在其他组织中表达水平较低。在所有检测的组织中,ZmPR10.1 的表达水平均明显低于 ZmPR10。ZmPR10 和 ZmPR10.1 的表达均被大多数非生物胁迫诱导,包括在 16 小时处理期间 SA、CuCl(2)、H(2)O(2)、寒冷、黑暗和创伤,以及生物胁迫如欧文氏菌和黄曲霉感染。然而,ZmPR10.1 仅在 2 小时后被诱导,此后下调,而 ZmPR10 在 16 小时的 NAA 处理期间仍被诱导。此外,接种欧文氏菌可使 ZmPR10.1 的表达在 60 小时后增加约 2 倍,但对 ZmPR10 的表达没有显著影响。ZmPR10.1 和 ZmPR10 在体外均具有 RNA 酶活性,最适 pH 和温度分别为 6.5 和 55 摄氏度。低浓度(1.0mM)的 Cu(2+)、Ag(+)、Co(2+)、SDS、EDTA 或 DTT 可显著抑制其 RNA 酶活性。然而,ZmPR10.1 的特异性 RNA 酶活性比 ZmPR10 高 8 倍。此外,ZmPR10.1 对番茄丁香假单胞菌 DC3000 细菌和黄曲霉真菌的体内抑制作用强于 ZmPR10,表明 ZmPR10.1 可能在宿主植物防御中也发挥重要作用。

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