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脱落酸和过氧化氢诱导一个新的玉米C组丝裂原活化蛋白激酶基因ZmMPK7,该基因负责清除活性氧。

Abscisic acid and hydrogen peroxide induce a novel maize group C MAP kinase gene, ZmMPK7, which is responsible for the removal of reactive oxygen species.

作者信息

Zong Xiao-juan, Li Da-peng, Gu Ling-kun, Li De-quan, Liu Li-xia, Hu Xiao-li

机构信息

Shandong Agricultural University, 271018, Taian, Shandong, People's Republic of China.

出版信息

Planta. 2009 Feb;229(3):485-95. doi: 10.1007/s00425-008-0848-4. Epub 2008 Nov 11.

DOI:10.1007/s00425-008-0848-4
PMID:19002491
Abstract

Mitogen-activated protein kinase (MAPK) cascades are involved in biotic and abiotic stress responses. In plants, MAPKs are classified into four groups, designated A-D. Information about group C MAPKs is limited, and, in particular, no data from maize are available. In this article, we isolated a novel group C MAPK gene, ZmMPK7, from Zea mays. Exogenous abscisic acid (ABA) and hydrogen peroxide (H(2)O(2)) induced calcium-dependant transcription of ZmMPK7. Induction of this gene in response to ABA was blocked by several reactive oxygen species (ROS) manipulators such as imidazole, Tiron, and dimethylthiourea (DMTU). This result indicates that endogenous H(2)O(2) may be required for ZmMPK7-mediated ABA signaling. Expression of ZmMPK7 in Nicotonia tobaccum caused less H(2)O(2) to accumulate and alleviated ROS-mediated injuries following submission of the plants to osmotic stress. The enhanced total peroxidase (POD) activity in transgenic tobacco plants may contribute to removal of ROS. Finally, we have shown that the ZmMPK7 protein localizes in the nucleus. These results broaden our knowledge regarding plant group C MAPK activity in response to stress signals.

摘要

丝裂原活化蛋白激酶(MAPK)级联反应参与生物和非生物胁迫应答。在植物中,MAPK分为A-D四组。关于C组MAPK的信息有限,特别是没有来自玉米的数据。在本文中,我们从玉米中分离出一个新的C组MAPK基因ZmMPK7。外源脱落酸(ABA)和过氧化氢(H₂O₂)诱导ZmMPK7的钙依赖性转录。该基因对ABA的应答诱导被几种活性氧(ROS)调节剂如咪唑、钛铁试剂和二甲基硫脲(DMTU)阻断。这一结果表明,ZmMPK7介导的ABA信号传导可能需要内源性H₂O₂。ZmMPK7在烟草中的表达导致较少的H₂O₂积累,并减轻了植物遭受渗透胁迫后ROS介导的损伤。转基因烟草植株中总过氧化物酶(POD)活性的增强可能有助于ROS的清除。最后,我们证明了ZmMPK7蛋白定位于细胞核。这些结果拓宽了我们对植物C组MAPK响应胁迫信号活性的认识。

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