主要结论
毛竹 TEOSINTE BRANCHED 1、CYCLOIDEA 和增殖细胞因子 (TCP) 转录因子的生物信息学分析揭示了它们在非生物胁迫响应中的保守性和变异性以及可能的生物学功能。在拟南芥中过度表达PheTCP9表明它可能在盐胁迫反应的不同方面表现出新的视野。
抽象的
植物特异性 TCPs 在植物生长发育和胁迫响应中发挥着重要作用,但对毛竹 TCP 的研究有限。因此,本研究共从毛竹基因组中鉴定和表征了40个TCP基因(PheTCP1 ~ 40),并分为三个不同的亚科,即TEOSINTE BRANCHED 1 / CYCLOIDEA (TB1/CYC)中的7个,CINCINNATA中的14个。 (CIN) 和增殖细胞因子 (PCF) 中的 19。随后,我们分析了这些基因的基因结构和保守结构域,发现来自同一亚科的成员表现出相似的外显子/内含子分布模式。选择压力和基因重复分析结果表明,PheTCP基因在进化过程中经历了强烈的纯化选择。PheTCP基因的上游启动子区域存在许多与植物激素和胁迫响应相关的顺式元件,如ABRE、CGTCA-motif和ARE。亚细胞定位实验表明,PheTCP9 是一种核定位蛋白。如β-葡萄糖醛酸酶(GUS)活性所示,盐胁迫显着表明了PheTCP9的启动子。PheTCP9在毛竹的根、茎和叶中被显着诱导。NaCl溶液也显着诱导。过表达PheTCP9增加了转基因拟南芥的耐盐性。同时,H 2 O 2PheTCP9过表达(OE)转基因拟南芥中丙二醛(MDA)含量显着低于WT。在盐条件下,转基因拟南芥中的过氧化氢酶 (CAT) 活性、K + /Na +比率以及 CAT2 表达水平也比 WT 有很大提高。此外,在NaCl条件下, PheTCP9 OE转基因拟南芥的幼苗存活率高于WT。这些结果表明PheTCP9在盐分条件下对植物具有正向调节作用。
"点击查看英文标题和摘要"
Identification of TCP family in moso bamboo (Phyllostachys edulis) and salt tolerance analysis of PheTCP9 in transgenic Arabidopsis
Main conclusion
Bioinformatic analysis of moso bamboo TEOSINTE BRANCHED 1, CYCLOIDEA, and PROLIFERATING CELL FACTORS (TCP) transcription factors reveals their conservation and variation as well as the probable biological functions in abiotic stress response. Overexpressing PheTCP9 in Arabidopsis thaliana illustrates it may exhibit a new vision in different aspects of response to salt stress.
Abstract
Plant specific TCPs play important roles in plant growth, development and stress response, but studies of TCP in moso bamboo are limited. Therefore, in this study, a total of 40 TCP genes (PheTCP1 ~ 40) were identified and characterized from moso bamboo genome and divided into three different subfamilies, namely, 7 in TEOSINTE BRANCHED 1 / CYCLOIDEA (TB1/CYC), 14 in CINCINNATA (CIN) and 19 in PROLIFERATING CELL FACTOR (PCF). Subsequently, we analyzed the gene structures and conserved domain of these genes and found that the members from the same subfamilies exhibited similar exon/intron distribution patterns. Selection pressure and gene duplication analysis results indicated that PheTCP genes underwent strong purification selection during evolution. There were many cis-elements related to phytohermone and stress responsive existing in the upstream promoter regions of PheTCP genes, such as ABRE, CGTCA-motif and ARE. Subcellular localization experiments showed that PheTCP9 was a nuclear localized protein. As shown by β-glucuronidase (GUS) activity, the promoter of PheTCP9 was significantly indicated by salt stress. PheTCP9 was significantly induced in the roots, stems and leaves of moso bamboo. It was also significantly induced by NaCl solution. Overexpressing PheTCP9 increased the salt tolerance of transgenic Arabidopsis. Meanwhile, H2O2 and malondialdehyde (MDA) contents were significantly lower in PheTCP9 over expression (OE) transgenic Arabidopsis than WT. Catalase (CAT) activity, K+/Na+ ratio as well as CAT2 expression level was also much improved in transgenic Arabidopsis than WT under salt conditions. In addition, PheTCP9 OE transgenic Arabidopsis held higher survival rates of seedlings than WT under NaCl conditions. These results showed the positive regulation functions of PheTCP9 in plants under salt conditions.