High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors

This protocol describes how to perform northern blot analyses to detect microRNAs and their precursors with single-nucleotide resolution, which is crucial for analyzing individual length variants and for evaluating relative quantities of unique microRNAs in cells. Northern blot analysis consists of...

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Main Authors: Edyta Koscianska, Julia Starega-Roslan, Katarzyna Czubala, Wlodzimierz J. Krzyzosiak
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2011.11
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spelling doaj-6a69e369596b4516b400e7fd283efb272020-11-25T00:28:50ZengHindawi LimitedThe Scientific World Journal1537-744X2011-01-011110211710.1100/tsw.2011.11High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their PrecursorsEdyta Koscianska0Julia Starega-Roslan1Katarzyna Czubala2Wlodzimierz J. Krzyzosiak3Laboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, PolandLaboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, PolandLaboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, PolandLaboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, PolandThis protocol describes how to perform northern blot analyses to detect microRNAs and their precursors with single-nucleotide resolution, which is crucial for analyzing individual length variants and for evaluating relative quantities of unique microRNAs in cells. Northern blot analysis consists of resolving RNAs by gel electrophoresis, followed by transferring and fixing to nylon membranes as well as detecting by hybridization with radioactive probes. Earlier efforts to improve this method focused mainly on altering the sensitivity of short RNA detection. We have enhanced the resolution of the northern blot technique by optimizing the electrophoresis step. We have also investigated other steps of the procedure with the goal of enhancing the resolution of RNAs; herein, we present several recommendations to do so. Our protocol is applicable to analyses of all kinds of endogenous and exogenous RNAs, falling within length ranges of 20–30 and 50–70 nt, corresponding to microRNA and pre-microRNA lengths, respectively.http://dx.doi.org/10.1100/tsw.2011.11
collection DOAJ
language English
format Article
sources DOAJ
author Edyta Koscianska
Julia Starega-Roslan
Katarzyna Czubala
Wlodzimierz J. Krzyzosiak
spellingShingle Edyta Koscianska
Julia Starega-Roslan
Katarzyna Czubala
Wlodzimierz J. Krzyzosiak
High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors
The Scientific World Journal
author_facet Edyta Koscianska
Julia Starega-Roslan
Katarzyna Czubala
Wlodzimierz J. Krzyzosiak
author_sort Edyta Koscianska
title High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors
title_short High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors
title_full High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors
title_fullStr High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors
title_full_unstemmed High-Resolution Northern Blot for a Reliable Analysis of MicroRNAs and Their Precursors
title_sort high-resolution northern blot for a reliable analysis of micrornas and their precursors
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2011-01-01
description This protocol describes how to perform northern blot analyses to detect microRNAs and their precursors with single-nucleotide resolution, which is crucial for analyzing individual length variants and for evaluating relative quantities of unique microRNAs in cells. Northern blot analysis consists of resolving RNAs by gel electrophoresis, followed by transferring and fixing to nylon membranes as well as detecting by hybridization with radioactive probes. Earlier efforts to improve this method focused mainly on altering the sensitivity of short RNA detection. We have enhanced the resolution of the northern blot technique by optimizing the electrophoresis step. We have also investigated other steps of the procedure with the goal of enhancing the resolution of RNAs; herein, we present several recommendations to do so. Our protocol is applicable to analyses of all kinds of endogenous and exogenous RNAs, falling within length ranges of 20–30 and 50–70 nt, corresponding to microRNA and pre-microRNA lengths, respectively.
url http://dx.doi.org/10.1100/tsw.2011.11
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