The choice of resuspension medium for isolated rat liver nuclei: effects on nuclear morphology and in vitro transcription

Standard protocols for in vitro transcription assay (nuclear run-off) include 10-40% (v/v) glycerol (of various ionic strength) in the medium used for resuspension/storage of the isolated nuclei. In the present work the morphological and functional properties of nuclei isolated from rat liver have b...

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Veröffentlicht in:Molecular and cellular biochemistry 1994-10, Vol.139 (2), p.149-157
Hauptverfasser: Strand, R, Bøe, R, Flatmark, T
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container_title Molecular and cellular biochemistry
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creator Strand, R
Bøe, R
Flatmark, T
description Standard protocols for in vitro transcription assay (nuclear run-off) include 10-40% (v/v) glycerol (of various ionic strength) in the medium used for resuspension/storage of the isolated nuclei. In the present work the morphological and functional properties of nuclei isolated from rat liver have been studied as a function of the content of glycerol, sucrose and inorganic ions (K+ and Mg2+) in the resuspension medium. In contrast to earlier reports, glycerol was found not to be essential to maintain morphological integrity and RNA polymerase activity in frozen/stored nuclei. Nuclear pellets, resuspended and stored in isoosmotic sucrose media, were found to give morphologically intact and transcriptionally active nuclei. Furthermore, these nuclei displayed a higher specific hybridization signal for the differentially expressed genes encoding peroxisomal beta-oxidation enzymes, relative to the total RNA synthesis, than nuclei resuspended and stored in a hyperosmotic glycerol-containing medium. The concentrations of inorganic ions were also found to affect nuclear morphology. Flow cytometry indicated DNA leakage from nuclei at insufficient concentrations of K+ and Mg2+, and high ionic strength favoured aggregation and disintegration of nuclei. Our findings indicate that quantitative results from nuclear run-off experiments should be interpreted with caution until the process of transcription in isolated nuclei is better understood.
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In the present work the morphological and functional properties of nuclei isolated from rat liver have been studied as a function of the content of glycerol, sucrose and inorganic ions (K+ and Mg2+) in the resuspension medium. In contrast to earlier reports, glycerol was found not to be essential to maintain morphological integrity and RNA polymerase activity in frozen/stored nuclei. Nuclear pellets, resuspended and stored in isoosmotic sucrose media, were found to give morphologically intact and transcriptionally active nuclei. Furthermore, these nuclei displayed a higher specific hybridization signal for the differentially expressed genes encoding peroxisomal beta-oxidation enzymes, relative to the total RNA synthesis, than nuclei resuspended and stored in a hyperosmotic glycerol-containing medium. The concentrations of inorganic ions were also found to affect nuclear morphology. Flow cytometry indicated DNA leakage from nuclei at insufficient concentrations of K+ and Mg2+, and high ionic strength favoured aggregation and disintegration of nuclei. 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Flow cytometry indicated DNA leakage from nuclei at insufficient concentrations of K+ and Mg2+, and high ionic strength favoured aggregation and disintegration of nuclei. Our findings indicate that quantitative results from nuclear run-off experiments should be interpreted with caution until the process of transcription in isolated nuclei is better understood.</description><subject>Animals</subject><subject>Cell Fractionation</subject><subject>Cell Nucleus - drug effects</subject><subject>Cell Nucleus - enzymology</subject><subject>Cell Nucleus - genetics</subject><subject>Cell Nucleus - ultrastructure</subject><subject>Cryoprotective Agents - pharmacology</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>Female</subject><subject>Glycerol - pharmacology</subject><subject>Liver - metabolism</subject><subject>Liver - ultrastructure</subject><subject>Magnesium Chloride - pharmacology</subject><subject>Male</subject><subject>Microbodies - enzymology</subject><subject>Osmolar Concentration</subject><subject>Potassium Chloride - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>Sucrose - pharmacology</subject><subject>Transcription, Genetic</subject><issn>0300-8177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotUD1PwzAQ9QAqpbCwI93EFjgnTZywQUUBqRJLmSPHORMjJw62U6n_ngg6ne7eh-49xm443nNE8fC8RY4lF1l5xpaYISbzIi7YZQjfOEPI-YItRFmkHPMlO-47AtU5owicBk9hCiMNwbgBemrN1IN2HkxwVkZqwcsI1hzIwzApS-YRSGtSMcAs-DtJD73zY-es-zqCHFowAxxM9A6il0NQ3oxxtr9i51raQNenuWKf25f95i3Zfby-b552yZhiEZOiyCutm6zMyyoVTcu1XqepKkgqFFXKSRIKiQVqnimJpDllqpKamiqfP2uzFbv79x29-5koxLo3QZG1ciA3hVoIUfB1hTPx9kScmjl6PXrTS3-sT11lv7RTa8w</recordid><startdate>19941026</startdate><enddate>19941026</enddate><creator>Strand, R</creator><creator>Bøe, R</creator><creator>Flatmark, T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19941026</creationdate><title>The choice of resuspension medium for isolated rat liver nuclei: effects on nuclear morphology and in vitro transcription</title><author>Strand, R ; Bøe, R ; Flatmark, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p206t-6659ffb3858927bd1ff422c6eac07921eae07a060f13ca0ef1e3c9afeb95ffed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Cell Fractionation</topic><topic>Cell Nucleus - drug effects</topic><topic>Cell Nucleus - enzymology</topic><topic>Cell Nucleus - genetics</topic><topic>Cell Nucleus - ultrastructure</topic><topic>Cryoprotective Agents - pharmacology</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>Female</topic><topic>Glycerol - pharmacology</topic><topic>Liver - metabolism</topic><topic>Liver - ultrastructure</topic><topic>Magnesium Chloride - pharmacology</topic><topic>Male</topic><topic>Microbodies - enzymology</topic><topic>Osmolar Concentration</topic><topic>Potassium Chloride - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Sucrose - pharmacology</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strand, R</creatorcontrib><creatorcontrib>Bøe, R</creatorcontrib><creatorcontrib>Flatmark, T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strand, R</au><au>Bøe, R</au><au>Flatmark, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The choice of resuspension medium for isolated rat liver nuclei: effects on nuclear morphology and in vitro transcription</atitle><jtitle>Molecular and cellular biochemistry</jtitle><addtitle>Mol Cell Biochem</addtitle><date>1994-10-26</date><risdate>1994</risdate><volume>139</volume><issue>2</issue><spage>149</spage><epage>157</epage><pages>149-157</pages><issn>0300-8177</issn><abstract>Standard protocols for in vitro transcription assay (nuclear run-off) include 10-40% (v/v) glycerol (of various ionic strength) in the medium used for resuspension/storage of the isolated nuclei. 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subjects Animals
Cell Fractionation
Cell Nucleus - drug effects
Cell Nucleus - enzymology
Cell Nucleus - genetics
Cell Nucleus - ultrastructure
Cryoprotective Agents - pharmacology
DNA-Directed RNA Polymerases - metabolism
Female
Glycerol - pharmacology
Liver - metabolism
Liver - ultrastructure
Magnesium Chloride - pharmacology
Male
Microbodies - enzymology
Osmolar Concentration
Potassium Chloride - pharmacology
Rats
Rats, Wistar
RNA, Messenger - biosynthesis
RNA, Messenger - genetics
Sucrose - pharmacology
Transcription, Genetic
title The choice of resuspension medium for isolated rat liver nuclei: effects on nuclear morphology and in vitro transcription
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