Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.

RNA interference (RNAi) is a complex and highly conserved regulatory mechanism mediated via small RNAs (sRNAs). Recent technical advances in high throughput sequencing have enabled an increasingly detailed analysis of sRNA abundances and profiles in specific body parts and tissues. This enables inve...

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Main Authors: Emily K Fowler, Irina Mohorianu, Damian T Smith, Tamas Dalmay, Tracey Chapman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5825024?pdf=render
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author Emily K Fowler
Irina Mohorianu
Damian T Smith
Tamas Dalmay
Tracey Chapman
author_facet Emily K Fowler
Irina Mohorianu
Damian T Smith
Tamas Dalmay
Tracey Chapman
author_sort Emily K Fowler
collection DOAJ
description RNA interference (RNAi) is a complex and highly conserved regulatory mechanism mediated via small RNAs (sRNAs). Recent technical advances in high throughput sequencing have enabled an increasingly detailed analysis of sRNA abundances and profiles in specific body parts and tissues. This enables investigations of the localized roles of microRNAs (miRNAs) and small interfering RNAs (siRNAs). However, variation in the proportions of non-coding RNAs in the samples being compared can hinder these analyses. Specific tissues may vary significantly in the proportions of fragments of longer non-coding RNAs (such as ribosomal RNA or transfer RNA) present, potentially reflecting tissue-specific differences in biological functions. For example, in Drosophila, some tissues contain a highly abundant 30nt rRNA fragment (the 2S rRNA) as well as abundant 5' and 3' terminal rRNA fragments. These can pose difficulties for the construction of sRNA libraries as they can swamp the sequencing space and obscure sRNA abundances. Here we addressed this problem and present a modified "rRNA blocking" protocol for the construction of high-definition (HD) adapter sRNA libraries, in D. melanogaster reproductive tissues. The results showed that 2S rRNAs targeted by blocking oligos were reduced from >80% to < 0.01% total reads. In addition, the use of multiple rRNA blocking oligos to bind the most abundant rRNA fragments allowed us to reveal the underlying sRNA populations at increased resolution. Side-by-side comparisons of sequencing libraries of blocked and non-blocked samples revealed that rRNA blocking did not change the miRNA populations present, but instead enhanced their abundances. We suggest that this rRNA blocking procedure offers the potential to improve the in-depth analysis of differentially expressed sRNAs within and across different tissues.
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spelling doaj.art-a61154cb1a2340f9acc0e8bf98df12552022-12-22T01:04:58ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01132e019196610.1371/journal.pone.0191966Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.Emily K FowlerIrina MohorianuDamian T SmithTamas DalmayTracey ChapmanRNA interference (RNAi) is a complex and highly conserved regulatory mechanism mediated via small RNAs (sRNAs). Recent technical advances in high throughput sequencing have enabled an increasingly detailed analysis of sRNA abundances and profiles in specific body parts and tissues. This enables investigations of the localized roles of microRNAs (miRNAs) and small interfering RNAs (siRNAs). However, variation in the proportions of non-coding RNAs in the samples being compared can hinder these analyses. Specific tissues may vary significantly in the proportions of fragments of longer non-coding RNAs (such as ribosomal RNA or transfer RNA) present, potentially reflecting tissue-specific differences in biological functions. For example, in Drosophila, some tissues contain a highly abundant 30nt rRNA fragment (the 2S rRNA) as well as abundant 5' and 3' terminal rRNA fragments. These can pose difficulties for the construction of sRNA libraries as they can swamp the sequencing space and obscure sRNA abundances. Here we addressed this problem and present a modified "rRNA blocking" protocol for the construction of high-definition (HD) adapter sRNA libraries, in D. melanogaster reproductive tissues. The results showed that 2S rRNAs targeted by blocking oligos were reduced from >80% to < 0.01% total reads. In addition, the use of multiple rRNA blocking oligos to bind the most abundant rRNA fragments allowed us to reveal the underlying sRNA populations at increased resolution. Side-by-side comparisons of sequencing libraries of blocked and non-blocked samples revealed that rRNA blocking did not change the miRNA populations present, but instead enhanced their abundances. We suggest that this rRNA blocking procedure offers the potential to improve the in-depth analysis of differentially expressed sRNAs within and across different tissues.http://europepmc.org/articles/PMC5825024?pdf=render
spellingShingle Emily K Fowler
Irina Mohorianu
Damian T Smith
Tamas Dalmay
Tracey Chapman
Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.
PLoS ONE
title Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.
title_full Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.
title_fullStr Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.
title_full_unstemmed Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.
title_short Small RNA populations revealed by blocking rRNA fragments in Drosophila melanogaster reproductive tissues.
title_sort small rna populations revealed by blocking rrna fragments in drosophila melanogaster reproductive tissues
url http://europepmc.org/articles/PMC5825024?pdf=render
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AT damiantsmith smallrnapopulationsrevealedbyblockingrrnafragmentsindrosophilamelanogasterreproductivetissues
AT tamasdalmay smallrnapopulationsrevealedbyblockingrrnafragmentsindrosophilamelanogasterreproductivetissues
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