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Ahnert, S.

Publications and source records attributed to Ahnert, S..

3 recordsLinked to original sources

Analysis of phloem trajectory links tissue maturation to cell specialization.

The mechanisms that allow cells in the plant meristem to coordinate tissue-wide maturation gradients with specialized cell networks are critical for indeterminate growth. Here, we reconstructed the protophloem developmental trajectory of 19 cells from cell birth to terminal differentiation at single cell resolution in the Arabidopsis root. We found that cellular specification is mediated near the stem cell niche by PHLOEM EARLY DOF (PEAR) transcription factors. However, the PEAR dependent differentiation program is repressed by a broad gradient of PLETHORA (PLT) transcription factors, which directly inhibit PEARs own direct target ALTERED PHLOEM DEVELOPMENT (APL). The dissipation of PLT gradient around 7 cells from the stem cell activates APL expression, and a subsequent transitional network that results in a "seesaw" pattern of mutual inhibition over developmental time. Together, we provide a mechanistic understanding of how morphogen-like maturation gradients interface with cell-type specific transcriptional regulators to stage cellular differentiation.

plant biology↗

Co-expression networks from gene expression variability between genetically identical seedlings can reveal novel regulatory relationships

Co-expression networks are a powerful tool to understand gene regulation. They have been used to identify new regulation and function of genes involved in plant development and their response to the environment. Up to now, co-expression networks have been inferred using transcriptomes generated on plants experiencing genetic or environmental perturbation, or from expression time series. We propose a new approach by showing that co-expression networks can be constructed in the absence of genetic and environmental perturbation, for plants at the same developmental stage. For this we used transcriptomes that were generated from genetically identical individual plants that were grown in the same conditions and for the same amount of time. Twelve time points were used to cover the 24h light/dark cycle. We used variability in gene expression between individual plants of the same time point to infer a co-expression network. We show that this network is biologically relevant and use it to suggest new gene functions and to identify new targets for the transcription factors GI, PIF4 and PRR5. Moreover, we find different co-regulation in this network based on changes in expression between individual plants, compared to the usual approach requiring environmental perturbation. Our work shows that gene co-expression networks can be identified using variability in gene expression between individual plants, without the need for genetic or environmental perturbations. It will allow further exploration of gene regulation in contexts with subtle differences between plants, which could be closer to what individual plants in a population might face in the wild. Author summaryPlant development and response to changes in the environment are strongly regulated at the level of gene expression. That is why understanding how gene expression is regulated is key, and transcriptome approaches have allowed the analysis of transcription for all genes of the genome. Extracting useful information from the high amount of data generated by transcriptomes is a challenge, and gene co-expression networks are a powerful tool to do this. The principle is to find genes that co-vary in expression in different conditions and to pair them together. Communities of genes that are more closely linked are then identified and this is the starting point to look for their implication in the same pathway. Co-expression networks have been used to identify new regulation and function of genes involved in plant development and their response to the environment. They were constructed using transcriptomes generated on plants experiencing genetic or environmental perturbation. We show that co-expression networks can in fact be constructed in the absence of genetic and environmental perturbation. Our work will allow further exploration of gene co-regulation in contexts with subtle differences between plants, which could be closer to what individual plants in a population might face in the wild.

plant biology↗

Widespread inter-individual gene expression variability in Arabidopsis thaliana

A fundamental question in biology is how gene expression is regulated to give rise to a phenotype. However, transcriptional variability is rarely considered and could influence the relationship between genotype and phenotype. It is known in unicellular organisms that gene expression is often noisy rather than uniform and this has been proposed to be beneficial when environmental conditions are unpredictable. However, little is known about transcriptional variability in plants. Using transcriptomic approaches, we analysed gene expression variability between individual Arabidopsis thaliana plants growing in identical conditions over a 24 hour time-course. We identified hundreds of genes that exhibit high inter-individual variability and found that many are involved in environmental responses. We also identified factors that might facilitate gene expression variability, such as gene length, the number of transcription factors regulating the genes and the chromatin environment. These results shed new light on the impact of transcriptional variability in gene expression regulation in plants.

plant biology↗