Mohasseb Heba Allah A, Solliman Mohei El-Din, Al-Mssallem Ibrahim S, Abdullah Mohammed M Ba, Alsaqufi Ahmed Saud, Shehata Wael F, El-Shemy Hany A
Plant Biotechnology Department, College of Agricultural and Food Sciences, King Faisal University, P.O. Box 400, Al-Ahsa 31982, Saudi Arabia.
Plant Biotechnology Department, National Research Centre, Dokki-Egypt, Giza P.O. Box 12622, Cairo, Egypt.
Plants (Basel). 2020 Sep 29;9(10):1285. doi: 10.3390/plants9101285.
Plant response to salt stress and the mechanism of salt tolerance have received major focus by plant biology researchers. Biotic stresses cause extensive losses in agricultural production globally, but abiotic stress causes significant increase in the methylglyoxal (MG) level of (). Identification of salt-tolerant genes when characterizing their phenotypes will help to identify novel genes using polymerase chain reaction (PCR) to amplify the DNA coding region for . This method is specific, requiring only genomic DNA and two pairs of PCR primers, and involving two successive PCR reactions. This method was used rapidly and easily identified sequences as salt-tolerant genes from Jojoba ( (Link) Schneider). In the present study, the gene was isolated, amplified by PCR using gene-specific primers and sequenced from the jojoba plant, then compared with other sequences in other plants and genes like in , ID: KT720495.1; ID: Y13239.1, ; ID: DQ989209.2; and L, ID: AAL84986. The structural gene of , when sequenced and analyzed, revealed that the uninterrupted open reading frame (ORF) of jojoba () spans 775 bp, corresponding to 185 amino acid residues, and shares 45.2% amino acid sequence identity to jojoba (Jojo-Gly I). The cloned ORF, in a multicopy constitutive expression plasmid, complemented the , confirming that the encoded in jojoba showed some homology with other known sequences of plants.
植物对盐胁迫的响应及耐盐机制一直是植物生物学研究人员关注的重点。生物胁迫在全球范围内导致农业生产大量损失,但非生物胁迫会使()的甲基乙二醛(MG)水平显著升高。在对耐盐基因进行表型鉴定时,识别这些基因将有助于利用聚合酶链反应(PCR)扩增()的DNA编码区来鉴定新基因。该方法具有特异性,仅需基因组DNA和两对PCR引物,且涉及两个连续的PCR反应。此方法被快速且轻松地用于从霍霍巴((Link)Schneider)中鉴定出()序列作为耐盐基因。在本研究中,从霍霍巴植物中分离出()基因,使用基因特异性引物通过PCR进行扩增并测序,然后与其他植物中的其他()序列以及()基因(如,ID:KT720495.1;()ID:Y13239.1,();ID:DQ989209.2;以及()L,ID:AAL84986)进行比较。对()的结构基因进行测序和分析后发现,霍霍巴()的不间断开放阅读框(ORF)跨度为775 bp,对应185个氨基酸残基,与霍霍巴(Jojo - Gly I)的氨基酸序列同一性为45.2%。克隆的ORF在多拷贝组成型表达质粒中对()进行了互补,证实霍霍巴中编码的()与其他已知植物的()序列具有一定同源性。