Transposition plays a role in the epidemiology and pathogenesis of Neisseria meningitidis. Insertion sequences are involved in reversible capsulation and insertional inactivation of virulence genes encoding outer membrane proteins. In this study, we have investigated and identified one way in which transposon IS1106 controls its own activity. We have characterized a naturally occurring protein (Tip) that inhibits the transposase. The inhibitor protein is a truncated version of the IS1106 transposase lacking the NH(2)-terminal DNA binding sequence, and it regulates transposition by competing with the transposase for binding to the outside ends of IS1106, as shown by gel shift and in vitro transposition assays. IS1106Tip mRNA is variably expressed among serogroup B meningococcal clinical isolates, and it is absent in most collection strains belonging to hypervirulent lineages.
Identification, characterization, and variable expression of a naturally occuring inhibitor protein of IS1106 transposase in clinical isolates of Neisseria meningitidis / Salvatore, Paola; Pagliarulo, C.; Colicchio, Roberta; Zecca, P.; Cantalupo, G.; Tredici, M.; Lavitola, Alfredo; Bucci, C.; Bruni, CARMELO BRUNO; Alifano, P.. - In: INFECTION AND IMMUNITY. - ISSN 0019-9567. - 69:(2001), pp. 7425-7436. [10.1128/IAI.69.12.7425-7436.2001]
Identification, characterization, and variable expression of a naturally occuring inhibitor protein of IS1106 transposase in clinical isolates of Neisseria meningitidis
SALVATORE, PAOLA;COLICCHIO, ROBERTA;LAVITOLA, ALFREDO;BRUNI, CARMELO BRUNO;
2001
Abstract
Transposition plays a role in the epidemiology and pathogenesis of Neisseria meningitidis. Insertion sequences are involved in reversible capsulation and insertional inactivation of virulence genes encoding outer membrane proteins. In this study, we have investigated and identified one way in which transposon IS1106 controls its own activity. We have characterized a naturally occurring protein (Tip) that inhibits the transposase. The inhibitor protein is a truncated version of the IS1106 transposase lacking the NH(2)-terminal DNA binding sequence, and it regulates transposition by competing with the transposase for binding to the outside ends of IS1106, as shown by gel shift and in vitro transposition assays. IS1106Tip mRNA is variably expressed among serogroup B meningococcal clinical isolates, and it is absent in most collection strains belonging to hypervirulent lineages.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.