Award details

A computational platform for the high-throughput identification of short RNAs and their targets in plants

Reference	BB/E004091/1
Principal Investigator / Supervisor	Professor Vincent Moulton
Co-Investigators / Co-Supervisors	Professor Sir David Baulcombe, Professor Tamas Dalmay
Institution	University of East Anglia
Department	Computing Sciences
Funding type	Research
Value (£)	250,576
Status	Completed
Type	Research Grant
Start date	26/02/2007
End date	25/02/2010
Duration	36 months

Abstract

A recently discovered layer of gene expression regulation in plants utilizes two types of small, non-coding regulatory RNAs (sRNAs): microRNAs (miRNAs) and small interfering RNAs (siRNAs). sRNAs can target RNA in a sequence-specific manner through base pairing between sRNAs and target RNAs. RNA targets of sRNAs are usually degraded in plants or in some cases translationally suppressed. sRNAs can also target genomic DNA causing methylation and heterochromatinisation that can lead to transcriptional gene silencing. Recent experimental studies indicate that there may be many thousands of sRNAs in plants, some of which are species specific. The laboratories of the co-PI's have set out to identify the full complement of sRNAs in different crop species. Their progress has been recently facilitated by a new high throughput pyrosequencing technology (www.454.com), which yields approximately 200,000 sRNA sequences for each sample. The aim of this project is to develop a computational platform to analyse the output from the co-PI's high-throughput sRNA sequencing projects. This platform will incorporate cutting-edge computational RNA analysis tools, and will allow both the classification of new sRNAs (some of which will be subjected to further experimental work), and the search for possible RNA targets. Identifying the full complement of sRNAs in different plant species will allow us to characterise an important and little understood layer of regulation in specific plant traits such as fleshy fruit development and ripening in tomato, and nitrogen fixation in alfalfa.

Summary

Most of the RNA molecules in cells are involved in protein production (ribosomal, transfer or messenger RNAs). However there are RNA molecules with other functions. Two classes of such non-coding RNAs which have been recently discovered are microRNAs (miRNAs) and small interfering RNAs (siRNAs). These regulatory RNA molecules are very short (19-24 nucleotides) and are thus commonly known as short RNAs (sRNAs). Some sRNAs can interact with specific mRNAs because they have partially complementary sequences. As a result of these interactions the expression of the targeted mRNAs is significantly reduced. Other sRNAs can target the chromosomes and trigger DNA modification. More than a hundred miRNAs have been identified in plant species (Arabidopsis, rice and poplar). However, the total number of sRNAs in plants is much higher: A recent experimental study identified about 75,000 sRNAs in Arabidopsis. In addition, several miRNAs found in one species were absent from the other suggesting that there are miRNAs which are specific to certain groups of plants. To systematically identify sRNAs in plants, the co-PIs laboratories have started to use a novel high-throughput sequencing technology (454 pyrosequencing). Initially, they are studying Arabidopsis and later, as the genome sequences will become available, tomato and alfalfa sRNAs will be analysed. This novel technology produces about 200,000 sRNA sequences for each sample. Preliminary results from the 454 technology are currently processed manually using standard bioinformatics tools. However, such an analysis is unfeasible for the millions of sRNA sequences that will be derived from future 454 experiments. The main goal of this project is to develop a computational platform dedicated to the analysis of data generated by the high-throughput 454 sRNA sequencing projects. This platform will classify new sRNAs, some of which will be subjected to further experimental work, and search for possible RNA targets. It will be initially tested on 454 data from Arabidopis, and subsequently on tomato and alfalfa. Later in the project, a comparative analysis tools will be incorporated for mutant analysis. New bioinformatics tools and novel sRNAs discovered through this project will be made publically available. Identifying the full complement of sRNAs in different plant species will allow us to characterise an important and little understood layer of regulation in specific plant traits such as fleshy fruit development and ripening in tomato, and nitrogen fixation in alfalfa.

Committee	Closed Committee - Plant & Microbial Sciences (PMS)
Research Topics	Crop Science, Plant Science
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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