Repression of IS200 transposase synthesis by RNA secondary structures

The IS200 transposase, a 16 kDa polypeptide encoded by the single open reading frame (ORF) of the insertion element, has been identified using an expression system based on T7 RNA polymerase. In wild-type IS200, two sets of internal inverted repeats that generate RNA secondary structures provide two...

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Detalles Bibliográficos
Autores: Beuzón López, Carmen del Rosario, Marqués, Silvia, Casadesús Pursals, Josep
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:1999
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/57427
Acceso en línea:http://hdl.handle.net/11441/57427
https://doi.org/10.1093/nar/27.18.3690
Access Level:acceso abierto
Palabra clave:Messenger RNA
RNA directed DNA polymerase
Transposase
Descripción
Sumario:The IS200 transposase, a 16 kDa polypeptide encoded by the single open reading frame (ORF) of the insertion element, has been identified using an expression system based on T7 RNA polymerase. In wild-type IS200, two sets of internal inverted repeats that generate RNA secondary structures provide two independent mechanisms for repression of transposase synthesis. The inverted repeat located near the left end of IS200 is a transcriptional terminator that terminates read-through transcripts before they reach the IS200 ORF. The terminator is functional in both directions and may terminate > 80% of transcripts. Another control operates at the translational level: transposase synthesis is inhibited by occlusion of the ribosome-binding site (RBS) of the IS200 ORF. The RBS (5'-AGGGG-3') is occluded by formation of a mRNA stem-loop structure whose 3' end is located only 3 nt upstream of the start codon. This mechanism reduces transposase synthesis ~ 10-fold. Primer extension experiments with AMV reverse transcriptase have provided evidence that this stem-loop RNA structure is actually formed. Tight repression of transposase synthesis, achieved through synergistic mechanisms of negative control, may explain the unusually low transposition frequency of IS200.