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叶片衰老及 27 种促进衰老的激素、病理和环境胁迫处理诱导的基因表达谱的收敛和发散。

Convergence and divergence in gene expression profiles induced by leaf senescence and 27 senescence-promoting hormonal, pathological and environmental stress treatments.

机构信息

Department of Horticulture, Cornell University, Ithaca, NY 14853-5904, USA.

出版信息

Plant Cell Environ. 2012 Mar;35(3):644-55. doi: 10.1111/j.1365-3040.2011.02442.x. Epub 2011 Nov 4.

Abstract

In addition to age and developmental progress, leaf senescence and senescence-associated genes (SAGs) can be induced by other factors such as plant hormones, pathogen infection and environmental stresses. The relationship is not clear, however, between these induced senescence processes and developmental leaf senescence, and to what extent these senescence-promoting signals mimic age and developmental senescence in terms of gene expression profiles. By analysing microarray expression data from 27 different treatments (that are known to promote senescence) and comparing them with that from developmental leaf senescence, we were able to show that at early stages of treatments, different hormones and stresses showed limited similarity in the induction of gene expression to that of developmental leaf senescence. Once the senescence process is initiated, as evidenced by visible yellowing, generally after a prolonged period of treatments, a great proportion of SAGs of developmental leaf senescence are shared by gene expression profiles in response to different treatments. This indicates that although different signals that lead to initiation of senescence may do so through distinct signal transduction pathways, senescence processes induced either developmentally or by different senescence-promoting treatments may share common execution events.

摘要

除了年龄和发育进程外,叶片衰老和衰老相关基因(SAGs)也可以被其他因素诱导,如植物激素、病原体感染和环境胁迫等。然而,这些诱导衰老过程与发育性叶片衰老之间的关系尚不清楚,而且这些促进衰老的信号在基因表达谱方面在多大程度上模拟了年龄和发育性衰老。通过分析 27 种不同处理(已知可促进衰老)的微阵列表达数据,并将其与发育性叶片衰老的表达数据进行比较,我们发现,在处理的早期阶段,不同激素和胁迫诱导基因表达与发育性叶片衰老的相似性有限。一旦衰老过程开始,表现为明显的黄化,通常是在长时间处理后,发育性叶片衰老的大量 SAGs 在对不同处理的基因表达谱中共享。这表明,尽管导致衰老开始的不同信号可能通过不同的信号转导途径进行,但通过不同的衰老促进处理诱导的衰老过程可能共享共同的执行事件。

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