Multiple products from functional RNA gene loci

来自功能性 RNA 基因位点的多种产物

• 批准号: BB/G011346/1
• 负责人: Sam Griffiths-Jones
• 金额: $ 43.29万
• 依托单位: University of Manchester
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2009
• 资助国家: 英国
• 起止时间: 2009 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FG011346%2F1
• 关键词: Multiple; products; functional; RNA; gene

The most commonly understood role of RNA is as an intermediate in the decoding of genetic information in DNA into the proteins that carry out the majority of known structural and functional roles in the cell. A few other classes of functional RNA (fRNA) molecules, such as transfer RNAs, ribosomal RNAs and spliceosomal RNAs, are expressed from their own genes (so-called RNA genes), but were long assumed to be unusual specialised cases. However, it is becoming clear that RNA molecules have many previously unimagined functions, including regulation of gene expression, as guide molecules, in imprinting, dosage compensation, catalysis and structure. Particular RNA classes have also been implicated in disease, including cancer. A number of new RNA classes have been discovered, including microRNAs (in 2001), riboswitches (in 2002) and piwi-associated RNAs (in 2006). Over 2000 functional RNA genes can now be identified in the human genome, making up around 10% of the total gene count. While there has been rapid progress in identifying novel RNAs, the functions of the majority of new discoveries are unknown. In addition, computational studies and large-scale transcriptional data predict that the majority of RNA genes remain to be discovered. There are hints that there may be as many RNA genes as there are protein-coding genes. Just as post-genomic science begins to approach understanding of the complete set of protein structures and functions encoded in the genome, the importance of the roles of RNA in regulating cellular processes is becoming clear. Previous work (including our own) has shown that many classes of functional RNA molecules are expressed from gene loci that also make proteins or other RNA products. This observation fundamentally challenges our concept of the gene. For example, a researcher who knocks-out a gene will likely assume that an observed phenotype is the result of loss of protein function. However, an ignored fRNA product, such as a microRNA, expressed from the same locus may regulate the expression of other genes, confounding the interpretation of experimental data. The proposed research aims to use the context of RNA gene loci in the genome to understand their function. For example, if a single gene or transcript produces a functional RNA and a translated protein at the same time in the same cells under the same conditions, we predict that the RNA and protein will have related functions, or be involved in related pathways. A few known examples, such as small nucleolar RNAs expressed from introns of ribosomal protein genes, suggest that this is the case, but no large-scale systematic study has been reported. The work will examine whether intronic RNAs are indeed processed from the host transcript, or expressed from their own promoters. We will test whether co-expressed RNA and protein products function in the same pathways. Finally, we will use our improved understanding of intronic RNA characteristics to predict novel functional RNAs.

The most commonly understood role of RNA is as an intermediate in the decoding of genetic information in DNA into the proteins that carry out the majority of known structural and functional roles in the cell. A few other classes of functional RNA (fRNA) molecules, such as transfer RNAs, ribosomal RNAs and spliceosomal RNAs, are expressed from their own genes (so-called RNA genes), but were long assumed to be unusual specialised cases. However, it is becoming clear that RNA molecules have many previously unimagined functions, including regulation of gene expression, as guide molecules, in imprinting, dosage compensation, catalysis and structure. Particular RNA classes have also been implicated in disease, including cancer. A number of new RNA classes have been discovered, including microRNAs (in 2001), riboswitches (in 2002) and piwi-associated RNAs (in 2006). Over 2000 functional RNA genes can now be identified in the human genome, making up around 10% of the total gene count. While there has been rapid progress in identifying novel RNAs, the functions of the majority of new discoveries are unknown. In addition, computational studies and large-scale transcriptional data predict that the majority of RNA genes remain to be discovered. There are hints that there may be as many RNA genes as there are protein-coding genes. Just as post-genomic science begins to approach understanding of the complete set of protein structures and functions encoded in the genome, the importance of the roles of RNA in regulating cellular processes is becoming clear. Previous work (including our own) has shown that many classes of functional RNA molecules are expressed from gene loci that also make proteins or other RNA products. This observation fundamentally challenges our concept of the gene. For example, a researcher who knocks-out a gene will likely assume that an observed phenotype is the result of loss of protein function. However, an ignored fRNA product, such as a microRNA, expressed from the same locus may regulate the expression of other genes, confounding the interpretation of experimental data. The proposed research aims to use the context of RNA gene loci in the genome to understand their function. For example, if a single gene or transcript produces a functional RNA and a translated protein at the same time in the same cells under the same conditions, we predict that the RNA and protein will have related functions, or be involved in related pathways. A few known examples, such as small nucleolar RNAs expressed from introns of ribosomal protein genes, suggest that this is the case, but no large-scale systematic study has been reported. The work will examine whether intronic RNAs are indeed processed from the host transcript, or expressed from their own promoters. We will test whether co-expressed RNA and protein products function in the same pathways. Finally, we will use our improved understanding of intronic RNA characteristics to predict novel functional RNAs.

项目成果

Functional shifts in insect microRNA evolution.

• DOI: 10.1093/gbe/evq053
• 发表时间: 2010
• 期刊: Genome biology and evolution
• 影响因子: 3.3
• 作者: Marco A;Hui JH;Ronshaugen M;Griffiths-Jones S
• 通讯作者: Griffiths-Jones S

Multiple products from microRNA transcripts.

来自 microRNA 转录本的多种产品。

• DOI: 10.1042/bst20130035
• 发表时间: 2013
• 期刊: Biochemical Society transactions
• 影响因子: 3.9
• 作者: Marco A

Regulatory RNAs in the light of Drosophila genomics.

• DOI: 10.1093/bfgp/els033
• 发表时间: 2012-09
• 期刊: Briefings in functional genomics
• 影响因子: 4
• 作者: Marco A

MicroRNAs from the same precursor have different targeting properties.

• DOI: 10.1186/1758-907x-3-8
• 发表时间: 2012-09-27
• 期刊: Silence
• 作者: Marco A;Macpherson JI;Ronshaugen M;Griffiths-Jones S
• 通讯作者: Griffiths-Jones S

Structure, evolution and function of the bi-directionally transcribed iab-4/iab-8 microRNA locus in arthropods.

• DOI: 10.1093/nar/gks1445
• 发表时间: 2013-03-01
• 期刊: Nucleic acids research
• 影响因子: 14.9
• 作者: Hui JH;Marco A;Hunt S;Melling J;Griffiths-Jones S;Ronshaugen M
• 通讯作者: Ronshaugen M