Xu Yun-Feng, Li Da-Peng, Gu Ling-Kun, Hu Xiao-Li, Zong Xiao-Juan, Li De-Quan
Shandong Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricutural University, Tai'an 271018, China.
Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao. 2005 Apr;31(2):183-9.
According to the conserved motifs of plant protein phosphatase 2C gene, degenerate oligonucleotides were designed. A full cDNA sequence of PP2C gene from Zea mays L. roots was cloned by RT-PCR. It was named ZmPP2C and had 936 bp. Southern blot showed that the ZmPP2C gene was a low copy in the Zea mays genome, and there was a small PP2C gene family. Northern blot showed that the expression of ZmPP2C gene was significantly different among Zea mays tissues. Zea mays roots treated with CaCl(2), MgCl(2), PEG, EGTA, and ABA for 24 h, the ZmPP2C expression increased only by CaCl(2) treatment. It showed the transcription of ZmPP2C gene was induced by Ca(2+), or in a Ca(2+)-dependent manner.
根据植物蛋白磷酸酶2C基因的保守基序设计了简并寡核苷酸。通过逆转录聚合酶链反应(RT-PCR)从玉米根中克隆了PP2C基因的完整cDNA序列。它被命名为ZmPP2C,长度为936 bp。Southern杂交表明ZmPP2C基因在玉米基因组中是低拷贝的,并且存在一个小的PP2C基因家族。Northern杂交表明ZmPP2C基因在玉米不同组织中的表达存在显著差异。用氯化钙(CaCl₂)、氯化镁(MgCl₂)、聚乙二醇(PEG)、乙二醇双(2-氨基乙醚)四乙酸(EGTA)和脱落酸(ABA)处理玉米根24小时,只有氯化钙处理使ZmPP2C表达增加。这表明ZmPP2C基因的转录受钙离子诱导,或以钙离子依赖的方式进行。