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Cloning, prokaryotic expression, and subcellular localisation of the TaMAPK10-like gene in common wheat

机译:克隆,原核表达和普通小麦中的茶袋型基因的亚细胞定位

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Mitogen-activated protein kinase (MAPK/MPK) is a group of serine-threonine protein kinases that are activated by different extracellular stimuli. To explore the function of MAPK in wheat infected with powdery mildew, a new wheat germplasm N9134 was used to obtain the full-length MAPK gene and the MAPK sequence was used to identify its prokaryotic expression and subcellular localisation. Wheat MAPK was obtained by homologous gene cloning and designated as TaMAPK10-like. The open reading frame of TaMAPKIO-like was 1638 bp, which coded a deduced protein of 545 amino acids. Phylogenetic analysis revealed that TaMAPK10-like was most closely related to MAPK10-like of Aegilops tauschii at the protein level. It had high nucleotide similarity with the reported MAPK gene in A. tauschii, Sorghum bicolor, and Setaria italica, and had features typical of MAPK family genes. Subcellular localisation showed that TaMAPK10-like was mainly located in the cytoplasm along the microtubules, and a small number were located in the cell membrane and the nucleus. A pMD-MAPK10-like fusion expression vector was constructed and the TaMAPK10-like fusion protein was 70 kDa. The expressions of protein in bacteria were best obtained using 0.5 mmol L-1 isopropyl beta-D-1-thiogalactopyranoside at 37 degrees C for 12 h. These results provide the basic data for further understanding the biological function of the TaMAPK10-like gene.
机译:丝裂原激活的蛋白激酶(MAPK / MPK)是一组由不同细胞外刺激激活的丝氨酸苏氨酸蛋白激酶。为了探讨Mapk在用粉末状霉菌感染的小麦中,使用新的小麦种质N9134来获得全长MAPK基因,MAPK序列用于鉴定其原核表达和亚细胞定位。小麦MAPK通过同源基因克隆获得并指定为Tamapk10样。 Tamapkio样的开放阅读框是1638 BP,编码了545个氨基酸的推导蛋白。系统发育分析显示,Tamapk10样与蛋白质水平的Aegilops Tauschii的Mapk10样最密切相关。它与A. Tauschii,高粱双子和棘皮素Italica的报告的Mapk基因具有高核苷酸相似性,并且具有典型的MAPK家族基因的特征。亚细胞定位表明,TamaPK10样主要位于沿微管中的细胞质中,并且少量位于细胞膜和细胞核中。构建了PMD-MAPK10样融合表达载体,并将Tamapk10样融合蛋白为70kDa。使用0.5mmol L-1异丙基β-D-1-硫代酰基吡喃钠,在37℃下最好地获得细菌中的蛋白质表达。这些结果提供了进一步了解TamaPK10样基因的生物学功能的基本数据。

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