Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins

<p>Abstract</p> <p>Background</p> <p>Short non-coding RNAs (ncRNAs) perform their cellular functions in ribonucleoprotein (RNP) complexes, which are also essential for maintaining the stability of the ncRNAs. Depletion of individual protein components of non-coding ribo...

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Main Authors: Skogerbø Geir, He Housheng, Aftab Muhammad, Chen Runsheng
Format: Article
Language:English
Published: BMC 2008-06-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/9/278
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spelling doaj-1023aea38145435389327375b6b24a462020-11-24T21:44:39ZengBMCBMC Genomics1471-21642008-06-019127810.1186/1471-2164-9-278Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteinsSkogerbø GeirHe HoushengAftab MuhammadChen Runsheng<p>Abstract</p> <p>Background</p> <p>Short non-coding RNAs (ncRNAs) perform their cellular functions in ribonucleoprotein (RNP) complexes, which are also essential for maintaining the stability of the ncRNAs. Depletion of individual protein components of non-coding ribonucleoprotein (ncRNP) particles by RNA interference (RNAi) may therefore affect expression levels of the corresponding ncRNA, and depletion of candidate associated proteins may constitute an alternative strategy when investigating ncRNA-protein interactions and ncRNA functions. Therefore, we carried out a pilot study in which the effects of RNAi against protein components of small nucleolar RNPs (snoRNPs) in <it>Caenorhabditis elegans </it>were observed on an ncRNA microarray.</p> <p>Results</p> <p>RNAi against individual <it>C. elegans </it>protein components of snoRNPs produced strongly reduced mRNA levels and distinct phenotypes for all targeted proteins. For each type of snoRNP, individual depletion of at least three of the four protein components produced significant (P ≦ 1.2 × 10<sup>-5</sup>) reductions in the expression levels of the corresponding small nucleolar RNAs (snoRNAs), whereas the expression levels of other ncRNAs were largely unaffected. The effects of depletion of individual proteins were in accordance with snoRNP structure analyses obtained in other species for all but two of the eight targeted proteins. Variations in snoRNA size, sequence and secondary structure characteristics were not systematically reflected in the affinity for individual protein component of snoRNPs. The data supported the classification of nearly all annotated snoRNAs and suggested the presence of several novel snoRNAs among unclassified short ncRNA transcripts. A number of transcripts containing canonical Sm binding element sequences (Sm Y RNAs) also showed reduced expression after depletion of protein components of C/D box snoRNPs, whereas the expression of some stem-bulge RNAs (sbRNAs) was increased after depletion of the same proteins.</p> <p>Conclusion</p> <p>The study confirms observations made for other organisms, where reduced ncRNA levels after depletion of protein components of ncRNPs were noted, and shows that such reductions in expression levels occur across entire sets of ncRNA. Thereby, the study also demonstrates the feasibility of combining RNAi against candidate proteins with ncRNA microarray analysis to investigate ncRNA-protein interactions and hence ncRNA cellular functions.</p> http://www.biomedcentral.com/1471-2164/9/278
collection DOAJ
language English
format Article
sources DOAJ
author Skogerbø Geir
He Housheng
Aftab Muhammad
Chen Runsheng
spellingShingle Skogerbø Geir
He Housheng
Aftab Muhammad
Chen Runsheng
Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins
BMC Genomics
author_facet Skogerbø Geir
He Housheng
Aftab Muhammad
Chen Runsheng
author_sort Skogerbø Geir
title Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins
title_short Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins
title_full Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins
title_fullStr Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins
title_full_unstemmed Microarray analysis of ncRNA expression patterns in <it>Caenorhabditis elegans </it>after RNAi against snoRNA associated proteins
title_sort microarray analysis of ncrna expression patterns in <it>caenorhabditis elegans </it>after rnai against snorna associated proteins
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2008-06-01
description <p>Abstract</p> <p>Background</p> <p>Short non-coding RNAs (ncRNAs) perform their cellular functions in ribonucleoprotein (RNP) complexes, which are also essential for maintaining the stability of the ncRNAs. Depletion of individual protein components of non-coding ribonucleoprotein (ncRNP) particles by RNA interference (RNAi) may therefore affect expression levels of the corresponding ncRNA, and depletion of candidate associated proteins may constitute an alternative strategy when investigating ncRNA-protein interactions and ncRNA functions. Therefore, we carried out a pilot study in which the effects of RNAi against protein components of small nucleolar RNPs (snoRNPs) in <it>Caenorhabditis elegans </it>were observed on an ncRNA microarray.</p> <p>Results</p> <p>RNAi against individual <it>C. elegans </it>protein components of snoRNPs produced strongly reduced mRNA levels and distinct phenotypes for all targeted proteins. For each type of snoRNP, individual depletion of at least three of the four protein components produced significant (P ≦ 1.2 × 10<sup>-5</sup>) reductions in the expression levels of the corresponding small nucleolar RNAs (snoRNAs), whereas the expression levels of other ncRNAs were largely unaffected. The effects of depletion of individual proteins were in accordance with snoRNP structure analyses obtained in other species for all but two of the eight targeted proteins. Variations in snoRNA size, sequence and secondary structure characteristics were not systematically reflected in the affinity for individual protein component of snoRNPs. The data supported the classification of nearly all annotated snoRNAs and suggested the presence of several novel snoRNAs among unclassified short ncRNA transcripts. A number of transcripts containing canonical Sm binding element sequences (Sm Y RNAs) also showed reduced expression after depletion of protein components of C/D box snoRNPs, whereas the expression of some stem-bulge RNAs (sbRNAs) was increased after depletion of the same proteins.</p> <p>Conclusion</p> <p>The study confirms observations made for other organisms, where reduced ncRNA levels after depletion of protein components of ncRNPs were noted, and shows that such reductions in expression levels occur across entire sets of ncRNA. Thereby, the study also demonstrates the feasibility of combining RNAi against candidate proteins with ncRNA microarray analysis to investigate ncRNA-protein interactions and hence ncRNA cellular functions.</p>
url http://www.biomedcentral.com/1471-2164/9/278
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