Jones Dallas C, Zheng Wenguang, Huang Sheng, Du Chuanlong, Zhao Xuefeng, Yennamalli Ragothaman M, Sen Taner Z, Nettleton Dan, Wurtele Eve S, Li Ling
Department of Genetics, Development and Cell Biology, Iowa State University, Ames IA, USA.
Department of Statistics, Iowa State University, Ames IA, USA.
Front Plant Sci. 2016 Jul 12;7:983. doi: 10.3389/fpls.2016.00983. eCollection 2016.
Nearly immobile, plants have evolved new components to be able to respond to changing environments. One example is Qua Quine Starch (QQS, AT3G30720), an Arabidopsis thaliana-specific orphan gene that integrates primary metabolism with adaptation to environment changes. SAQR (Senescence-Associated and QQS-Related, AT1G64360), is unique to a clade within the family Brassicaceae; as such, the gene may have arisen about 20 million years ago. SAQR is up-regulated in QQS RNAi mutant and in the apx1 mutant under light-induced oxidative stress. SAQR plays a role in carbon allocation: overexpression lines of SAQR have significantly decreased starch content; conversely, in a saqr T-DNA knockout (KO) line, starch accumulation is increased. Meta-analysis of public microarray data indicates that SAQR expression is correlated with expression of a subset of genes involved in senescence, defense, and stress responses. SAQR promoter::GUS expression analysis reveals that SAQR expression increases after leaf expansion and photosynthetic capacity have peaked, just prior to visible natural senescence. SAQR is expressed predominantly within leaf and cotyledon vasculature, increasing in intensity as natural senescence continues, and then decreasing prior to death. In contrast, under experimentally induced senescence, SAQR expression increases in vasculature of cotyledons but not in true leaves. In SAQR KO line, the transcript level of the dirigent-like disease resistance gene (AT1G22900) is increased, while that of the Early Light Induced Protein 1 gene (ELIP1, AT3G22840) is decreased. Taken together, these data indicate that SAQR may function in the QQS network, playing a role in integration of primary metabolism with adaptation to internal and environmental changes, specifically those that affect the process of senescence.
植物几乎不能移动,因此进化出了新的成分以便能够应对不断变化的环境。一个例子是四嗪淀粉(QQS,AT3G30720),这是拟南芥特有的一个孤儿基因,它将初级代谢与对环境变化的适应整合在一起。衰老相关且与QQS相关的基因(SAQR,AT1G64360)是十字花科内一个分支所特有的;因此,该基因可能大约在2000万年前出现。在光诱导的氧化应激下,SAQR在QQS RNA干扰突变体和apx1突变体中上调。SAQR在碳分配中起作用:SAQR的过表达株系淀粉含量显著降低;相反,在一个SAQR T-DNA敲除(KO)株系中,淀粉积累增加。对公共微阵列数据的荟萃分析表明,SAQR的表达与参与衰老、防御和应激反应的一部分基因的表达相关。SAQR启动子::GUS表达分析表明,在叶片扩展和光合能力达到峰值后,即在可见的自然衰老之前,SAQR的表达增加。SAQR主要在叶片和子叶脉管系统中表达,随着自然衰老的持续,表达强度增加,然后在死亡前降低。相反,在实验诱导的衰老过程中,SAQR在子叶脉管系统中表达增加,但在真叶中不增加。在SAQR KO株系中,类 dirigent 抗病基因(AT1G22900)的转录水平增加,而早期光诱导蛋白1基因(ELIP1,AT3G22840)的转录水平降低。综上所述,这些数据表明SAQR可能在QQS网络中发挥作用,在初级代谢与对内部和环境变化(特别是那些影响衰老过程的变化)的适应整合中发挥作用。