Document Detail


A combined immunoprecipitation, mass spectrometric and nucleic acid sequencing approach to determine microRNA-mediated post-transcriptional gene regulatory networks.
MedLine Citation:
PMID:  20053813     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
While initiation of transcription has attracted the most attention in the field of gene regulation, it has become clear that additional stages in the gene expression cascade including post-transcriptional events are under equally exquisite control. The seminal discovery that short RNAs (microRNA, small interfering RNA, Piwi-interacting RNA), play important roles in repressing gene expression has spurred a rush of new interest in post-transcriptional gene silencing mechanisms. The development of affinity tags and high-resolution tandem mass spectrometry (MS/MS) has greatly simplified the analysis of proteins that regulate gene expression. Further, the use of DNA microarrays and 'second generation' nucleic acid sequencing ('deep sequencing') technologies has facilitated the identification of their regulatory targets. These technological advancements mark a significant step towards a comprehensive understanding of gene regulatory networks. The purpose of this review is to highlight several recent reports that illustrate the value of affinity-purification (immunoprecipitation) followed by mass spectrometric protein analysis and nucleic acid analysis by deep sequencing (AP-MS/Seq) to examine mRNA after it has been transcribed. The ability to identify the direct nucleic acid targets of post-transcriptional gene regulatory machines is a critical first step towards understanding the contribution of post-transcriptional pathways on gene expression.
Authors:
Jeffrey N Savas; Naoko Tanese
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2010-01-06
Journal Detail:
Title:  Briefings in functional genomics     Volume:  9     ISSN:  2041-2657     ISO Abbreviation:  Brief Funct Genomics     Publication Date:  2010 Jan 
Date Detail:
Created Date:  2010-02-01     Completed Date:  2010-04-02     Revised Date:  2011-07-28    
Medline Journal Info:
Nlm Unique ID:  101528229     Medline TA:  Brief Funct Genomics     Country:  England    
Other Details:
Languages:  eng     Pagination:  24-31     Citation Subset:  IM    
Affiliation:
Department of Microbiology, NYU School of Medicine, 550 First Avenue, New York, NY 10016, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Gene Expression Profiling / methods
Gene Expression Regulation / genetics
Gene Regulatory Networks / genetics*
Humans
Immunoprecipitation / methods*
Mass Spectrometry / methods*
MicroRNAs / physiology*
Nucleic Acids / analysis
Oligonucleotide Array Sequence Analysis / methods
RNA Interference*
Sequence Analysis / methods*
Chemical
Reg. No./Substance:
0/MicroRNAs; 0/Nucleic Acids
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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