<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(1)</volume><submitter>Siddique A</submitter><funding>Wellcome Trust</funding><pubmed_abstract>Neisseria meningitidis is the primary causative agent of bacterial meningitis. The genome is rich in repetitive DNA and almost 2% is occupied by a diminutive transposon called the Correia element. Here we report a bioinformatic analysis defining eight subtypes of the element with four distinct types of ends. Transcriptional analysis, using PCR and a lacZ reporter system, revealed that two ends in particular encode strong promoters. The activity of the strongest promoter is dictated by a recurrent polymorphism (Y128) at the right end of the element. We highlight examples of elements that appear to drive transcription of adjacent genes and others that may express small non-coding RNAs. Pair-wise comparisons between three meningococcal genomes revealed that no more than two-thirds of Correia </pubmed_abstract><journal>PLoS genetics</journal><pagination>e1001277</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3024310</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The transposon-like Correia elements encode numerous strong promoters and provide a potential new mechanism for phase variation in the meningococcus.</pubmed_title><pmcid>PMC3024310</pmcid><pubmed_authors>Buisine N</pubmed_authors><pubmed_authors>Chalmers R</pubmed_authors><pubmed_authors>Siddique A</pubmed_authors></additional><is_claimable>false</is_claimable><name>The transposon-like Correia elements encode numerous strong promoters and provide a potential new mechanism for phase variation in the meningococcus.</name><description>Neisseria meningitidis is the primary causative agent of bacterial meningitis. The genome is rich in repetitive DNA and almost 2% is occupied by a diminutive transposon called the Correia element. Here we report a bioinformatic analysis defining eight subtypes of the element with four distinct types of ends. Transcriptional analysis, using PCR and a lacZ reporter system, revealed that two ends in particular encode strong promoters. The activity of the strongest promoter is dictated by a recurrent polymorphism (Y128) at the right end of the element. We highlight examples of elements that appear to drive transcription of adjacent genes and others that may express small non-coding RNAs. Pair-wise comparisons between three meningococcal genomes revealed that no more than two-thirds of Correia </description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jan</publication><modification>2026-05-02T07:43:24.167Z</modification><creation>2019-03-27T00:38:18Z</creation></dates><accession>S-EPMC3024310</accession><cross_references><pubmed>21283790</pubmed><doi>10.1371/journal.pgen.1001277</doi></cross_references></HashMap>