2009
DOI: 10.1186/1471-2105-10-325
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Riboswitch Detection Using Profile Hidden Markov Models

Abstract: Background: Riboswitches are a type of noncoding RNA that regulate gene expression by switching from one structural conformation to another on ligand binding. The various classes of riboswitches discovered so far are differentiated by the ligand, which on binding induces a conformational switch. Every class of riboswitch is characterized by an aptamer domain, which provides the site for ligand binding, and an expression platform that undergoes conformational change on ligand binding. The sequence and structure… Show more

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Cited by 35 publications
(31 citation statements)
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“…A purine riboswitch-specific pHMM7 was used to screen the bacterial genomes. A systematic analysis of the genomic context of purine riboswitches was carried out to identify the genes upstream to which riboswitches occur.…”
Section: Methodsmentioning
confidence: 99%
“…A purine riboswitch-specific pHMM7 was used to screen the bacterial genomes. A systematic analysis of the genomic context of purine riboswitches was carried out to identify the genes upstream to which riboswitches occur.…”
Section: Methodsmentioning
confidence: 99%
“…Thiamine pyrophosphate (TPP) is the most abundant riboswitch and is known to be present even in eukaryotes [37]. It has an intermediate level of sequence conservation [38]. So in many organisms (prokaryotes, algae, plants and fungi), riboswitch has been found to play the role of regulating thiamine biosynthesis [39].…”
Section: Thiamine Pyrophosphate: the Dominant Class Of Riboswitchmentioning
confidence: 99%
“…In contrast, while secondary structure is conserved in the terminator loop of the expression platform in purine riboswitches, there is relatively low sequence conservation (data not shown). While a number of methods exist to computationally predict riboswitch aptamers [31], [32], [33], [34], [35] (and especially INFERNAL [36], which latter is used to predict riboswitch aptamers in Rfam), it is an important biological problem to determine the expression platform, since the structure of the expression platform can suggest whether there is transcriptional regulation via a terminator loop or translational regulation via the sequestration of the Shine-Dalgarno sequence [28]. Determination of the precise location and structure of the expression platform is difficult due to low conserved sequence identity (in-house computations, data not shown).…”
Section: Resultsmentioning
confidence: 99%