Computational Biology in microRNA. (24th April 2015)
- Record Type:
- Journal Article
- Title:
- Computational Biology in microRNA. (24th April 2015)
- Main Title:
- Computational Biology in microRNA
- Authors:
- Li, Yue
Zhang, Zhaolei - Abstract:
- <abstract abstract-type="main" id="wrna1286-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="wrna1286-para-0001">MicroRNA (miRNA) is a class of small endogenous noncoding RNA species, which regulate gene expression post‐transcriptionally by forming imperfect base‐pair at the 3′ untranslated regions of the messenger RNAs. Since the 1993 discovery of the first miRNA <italic>let‐7</italic> in worms, a vast number of studies have been dedicated to functionally characterizing miRNAs with a special emphasis on their roles in cancer. A single miRNA can potentially target ∼400 distinct genes, and there are over a 1000 distinct endogenous miRNAs in the human genome. Thus, miRNAs are likely involved in virtually all biological processes and pathways including carcinogenesis. However, functionally characterizing miRNAs hinges on the accurate identification of their mRNA targets, which has been a challenging problem due to imperfect base‐pairing and condition‐specific miRNA regulatory dynamics. In this review, we will survey the current state‐of‐the‐art computational methods to predict miRNA targets, which are divided into three main categories: (1) sequence‐based methods that primarily utilizes the canonical seed‐match model, evolutionary conservation, and binding energy; (2) expression‐based target prediction methods using the increasingly available miRNA and mRNA expression data measured for the same sample; and (3) network‐based method that aims identify miRNA<abstract abstract-type="main" id="wrna1286-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="wrna1286-para-0001">MicroRNA (miRNA) is a class of small endogenous noncoding RNA species, which regulate gene expression post‐transcriptionally by forming imperfect base‐pair at the 3′ untranslated regions of the messenger RNAs. Since the 1993 discovery of the first miRNA <italic>let‐7</italic> in worms, a vast number of studies have been dedicated to functionally characterizing miRNAs with a special emphasis on their roles in cancer. A single miRNA can potentially target ∼400 distinct genes, and there are over a 1000 distinct endogenous miRNAs in the human genome. Thus, miRNAs are likely involved in virtually all biological processes and pathways including carcinogenesis. However, functionally characterizing miRNAs hinges on the accurate identification of their mRNA targets, which has been a challenging problem due to imperfect base‐pairing and condition‐specific miRNA regulatory dynamics. In this review, we will survey the current state‐of‐the‐art computational methods to predict miRNA targets, which are divided into three main categories: (1) sequence‐based methods that primarily utilizes the canonical seed‐match model, evolutionary conservation, and binding energy; (2) expression‐based target prediction methods using the increasingly available miRNA and mRNA expression data measured for the same sample; and (3) network‐based method that aims identify miRNA regulatory modules, which reflect their synergism in conferring a global impact to the biological system of interest. We hope that the review will serve as a good reference to the new comers to the ever‐growing miRNA research field as well as veterans, who would appreciate the detailed review on the technicalities, strength, and limitations of each representative computational method. <italic>WIREs RNA</italic> 2015, 6:435–452. doi: 10.1002/wrna.1286</p> <p>For further resources related to this article, please visit the <ext-link ext-link-type="uri" xlink:href="http://wires.wiley.com/remdoi.cgi?doi=10.1002/wrna.1286" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">WIREs website</ext-link>.</p> <p>Conflict of interest: The authors have declared no conflicts of interest for this article.</p> </abstract> … (more)
- Is Part Of:
- Wiley interdisciplinary reviews. Volume 6:Number 4(2015:Jul./Aug.)
- Journal:
- Wiley interdisciplinary reviews
- Issue:
- Volume 6:Number 4(2015:Jul./Aug.)
- Issue Display:
- Volume 6, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 6
- Issue:
- 4
- Issue Sort Value:
- 2015-0006-0004-0000
- Page Start:
- 435
- Page End:
- 452
- Publication Date:
- 2015-04-24
- Subjects:
- RNA -- Periodicals
572.8805 - Journal URLs:
- http://helicon.vuw.ac.nz/login?url=http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1757-7012 ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1757-7012 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/wrna.1286 ↗
- Languages:
- English
- ISSNs:
- 1757-7004
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9317.862404
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3496.xml