<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Aroonsri A</submitter><funding>National Science and Technology Development Agency (TH)</funding><funding>Thailand Research Fund</funding><funding>National Science and Technology Development Agency</funding><pagination>20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7967978</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Bioinformatic genome surveys indicate that self-cleaving ribonucleic acids (ribozymes) appear to be widespread among all domains of life, although the functions of only a small number have been validated by biochemical methods. Alternatively, cell-based reporter gene assays can be used to validate ribozyme function. However, reporter activity can be confounded by phenomena unrelated to ribozyme-mediated cleavage of RNA.&lt;h4>Results&lt;/h4>We established a ribozyme reporter system in Escherichia coli in which a significant reduction of reporter activity is manifest when an active ribozyme sequence is fused to the reporter gene and the expression of a foreign Bacillus subtilis RNaseJ1 5' exonuclease is induced from a chromosomally-integrated gene in the same cell.&lt;h4>Conclusio</pubmed_abstract><journal>BMC molecular and cell biology</journal><pubmed_title>A cell-based ribozyme reporter system employing a chromosomally-integrated 5' exonuclease gene.</pubmed_title><pmcid>PMC7967978</pmcid><funding_grant_id>P17-51076</funding_grant_id><funding_grant_id>TRG608001</funding_grant_id><pubmed_authors>Kongsee J</pubmed_authors><pubmed_authors>Shaw PJ</pubmed_authors><pubmed_authors>Aubry DA</pubmed_authors><pubmed_authors>Aroonsri A</pubmed_authors><pubmed_authors>Gunawan JD</pubmed_authors></additional><is_claimable>false</is_claimable><name>A cell-based ribozyme reporter system employing a chromosomally-integrated 5' exonuclease gene.</name><description>&lt;h4>Background&lt;/h4>Bioinformatic genome surveys indicate that self-cleaving ribonucleic acids (ribozymes) appear to be widespread among all domains of life, although the functions of only a small number have been validated by biochemical methods. Alternatively, cell-based reporter gene assays can be used to validate ribozyme function. However, reporter activity can be confounded by phenomena unrelated to ribozyme-mediated cleavage of RNA.&lt;h4>Results&lt;/h4>We established a ribozyme reporter system in Escherichia coli in which a significant reduction of reporter activity is manifest when an active ribozyme sequence is fused to the reporter gene and the expression of a foreign Bacillus subtilis RNaseJ1 5' exonuclease is induced from a chromosomally-integrated gene in the same cell.&lt;h4>Conclusio</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-05T13:48:26.011Z</modification><creation>2024-12-04T06:32:08.833Z</creation></dates><accession>S-EPMC7967978</accession><cross_references><pubmed>33726662</pubmed><doi>10.1186/s12860-021-00357-7</doi></cross_references></HashMap>