PLANT-RNA-MET · A newly discovered role for mRNA methylation in controlling plant gene expression
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2018-03-01 → 2020-12-17
- EU contribution
- €195,455
- Participants
- 1
- Scheme
- MSCA-IF-EF-ST
Lines connect the coordinator with its partners.
Results in brief
A newly discovered role for mRNA methylation in controlling plant gene expression
The ability of plants to grow, develop and respond to the environment depends upon the ability to precisely co-ordinate gene expression. As development proceeds, or defences to pathogens are mounted, the expression of some genes needs to be silenced, while other must be activated or amplified. Therefore, explaining how gene expression is regulated is important to understand how plant development and immunity are controlled. In many aspects, the principles of gene expression regulation in plants resemble that of other complex organisms, like humans or animals. Genes are segments of DNA, that during gene expression are transcribed by an enzyme called RNA polymerase II (Pol II) complexed with other components, into precursor messenger RNA (pre-mRNA). The efficiency of transcription depends on many factors, e.g DNA modifications that make DNA accessible or inaccessible to Pol II complexes. In the next step, pre-mRNA is processed in many ways into mature form - messenger mRNA (mRNA), that can affect mRNA fate in the cell. For example, the same pre-mRNA can be processed into mRNAs that differ in the position at which they end as a result of a process known as alternative polyadenylation. Since mRNA is next translated into protein, differences in pre-mRNA processing can determine what protein the gene will code for or what the lifetime of mRNA will be. Associated with pre-mRNA processing, is a newly recognised layer of gene regulation involving RNA modifications. For example, m6A RNA methylation is essential for regulation of mRNA fate, including mRNA degradation and translation efficiency. Our understanding of the diverse functional impacts of m6A in plants is still emerging. In this proposal, we aimed to explain the function of m6A mRNA modification in plant gene expression, with the major focus on plant immune response genes. To do this, we designed our experimental plan to recognise how m6A affects transcription termination and alternative polyadenylation, and to identify important factors involved in this regulation. Arabidopsis thaliana was used in this study because it is a model experimental system. A better understanding of the role of m6A in tuning gene expression in Arabidopsis facilitates the new knowledge and understanding required for the development of crops with improved growth and immunity against pathogens.
Data: CORDIS, © European Union
Project objective
Modifications to mRNA, collectively known as the epitranscriptome, comprise a neglected layer of gene regulation. The most abundant internal modification of mRNA is methylation of adenosine (m6A). The aim of this proposal is to explain a recently discovered interplay between mRNA methylation, gene silencing and gene expression in plants. Specific expressed Arabidopsis genes contain transposons within them that bear localised silencing marks that include methylation of DNA and modifications to histone proteins. The antagonism between stretches of so-called heterochromatin that should be “silent”, in genes that must be expressed, appears to provide a novel means to tune gene expression. Crucially, the Arabidopsis immune response gene RPP7 is regulated in this way. Recent findings suggest a link between mRNA methylation and intragenic heterochromatin: (1) The RNA binding protein FPA co-purifies with Arabidopsis m6A writers. (2) RNA-Sequencing analysis of fpa mutants and m6A writer complex mutants reveals changes in transcription through intragenic heterochromatin. (3) RNA-Sequencing maps m6A to intragenic heterochromatin. To determine the role of mRNA methylation in analyzed interplay, the order of events will be resolved by parallel measurement of heterochromatin (H3K9me2, m5C) and m6A marks in mutants defective in factors that control these marks. The directness by which FPA and mRNA methylation influences these events will be examined by ChIP-Seq and iCLIP-Seq of FPA and m6A writer complex components. The epigenetic stability of disrupting intragenic heterochromatin will be determined in stable lines with inducible FPA and m6A writer expression. Overall, we will assess a new role of mRNA methylation in tuning expression of crucially important plant genes.
Original text from CORDIS.
Participants
- UNIVERSITY OF DUNDEE · DundeeCoordinatorUnited Kingdom
Links
Data: CORDIS, © European Union
