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在蒺藜苜蓿根瘤发育过程中的转录重编程。

Transcription reprogramming during root nodule development in Medicago truncatula.

机构信息

Laboratoire des Interactions Plantes Micro-organismes, Centre National de la Recherche Scientifique, Institut National de la Recherche Agronomique, Castanet-Tolosan, France.

出版信息

PLoS One. 2011 Jan 27;6(1):e16463. doi: 10.1371/journal.pone.0016463.

Abstract

Many genes which are associated with root nodule development and activity in the model legume Medicago truncatula have been described. However information on precise stages of activation of these genes and their corresponding transcriptional regulators is often lacking. Whether these regulators are shared with other plant developmental programs also remains an open question. Here detailed microarray analyses have been used to study the transcriptome of root nodules induced by either wild type or mutant strains of Sinorhizobium meliloti. In this way we have defined eight major activation patterns in nodules and identified associated potential regulatory genes. We have shown that transcription reprogramming during consecutive stages of nodule differentiation occurs in four major phases, respectively associated with (i) early signalling events and/or bacterial infection; plant cell differentiation that is either (ii) independent or (iii) dependent on bacteroid differentiation; (iv) nitrogen fixation. Differential expression of several genes involved in cytokinin biosynthesis was observed in early symbiotic nodule zones, suggesting that cytokinin levels are actively controlled in this region. Taking advantage of databases recently developed for M. truncatula, we identified a small subset of gene expression regulators that were exclusively or predominantly expressed in nodules, whereas most other regulators were also activated under other conditions, and notably in response to abiotic or biotic stresses. We found evidence suggesting the activation of the jasmonate pathway in both wild type and mutant nodules, thus raising questions about the role of jasmonate during nodule development. Finally, quantitative RT-PCR was used to analyse the expression of a series of nodule regulator and marker genes at early symbiotic stages in roots and allowed us to distinguish several early stages of gene expression activation or repression.

摘要

许多与模式豆科植物苜蓿根瘤发育和活性相关的基因已经被描述。然而,关于这些基因的精确激活阶段及其相应的转录调控因子的信息通常是缺乏的。这些调控因子是否与其他植物发育程序共享也是一个悬而未决的问题。在这里,详细的微阵列分析被用于研究由野生型或突变型根瘤菌 Sinorhizobium meliloti 诱导的根瘤的转录组。通过这种方式,我们定义了根瘤中 8 种主要的激活模式,并鉴定了相关的潜在调节基因。我们已经表明,在连续的结瘤分化阶段,转录重编程发生在四个主要阶段,分别与(i)早期信号事件和/或细菌感染;植物细胞分化,是(ii)独立的或(iii)依赖于类菌体分化;(iv)氮固定。在早期共生结瘤区观察到几个参与细胞分裂素生物合成的基因的差异表达,表明细胞分裂素水平在该区域被主动控制。利用最近为苜蓿开发的数据库,我们鉴定了一小部分仅在根瘤中表达或主要在根瘤中表达的基因表达调控因子,而大多数其他调控因子也在其他条件下被激活,特别是在应对非生物或生物胁迫时。我们发现证据表明茉莉酸途径在野生型和突变型根瘤中被激活,因此提出了茉莉酸在根瘤发育过程中的作用问题。最后,定量 RT-PCR 用于分析在根中早期共生阶段一系列根瘤调节因子和标记基因的表达,并使我们能够区分基因表达激活或抑制的几个早期阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead6/3029352/2c50d2e73c46/pone.0016463.g001.jpg

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