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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003136naa a2200337 4500
001oai:DiVA.org:liu-25978
003SwePub
008091008s2001 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-259782 URI
024a https://doi.org/10.1046/j.1523-5378.2001.00015.x2 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Monstein, Hans-Jurg,d 1946-u Linköpings universitet,Hälsouniversitetet,Institutionen för hälsa och miljö4 aut0 (Swepub:liu)hanmo19
2451 0a Probing 23S ribosomal RNA cleavage sites in coccoid Helicobater pylori.
264 1b Wiley,c 2001
338 a print2 rdacarrier
520 a Background. Previous studies have revealed that extensive nonrandom fragmentation of ribosomal RNA occurs during conversion of Helicobacter pylori to the coccoid form. The 16S rRNA fragmentation has been characterised in some detail. The aim of the present study was to define corresponding cleavage-sites in the 3'-half of the 23S rRNA molecule. Materials and Methods. Northern blot analysis using 23S rRNA specific antisense riboprobes and a 5'-end- labelled oligonucleotide probe was used to analyse the 23S rRNA fragmentation pattern in coccoid H. pylori type strain CCUG 17874T and H. pylori 26695, for which the genome has been sequenced. A double- stranded cDNA-dependent (ds-cDNA) primer- extension analysis technique using 23S rRNA ds-cDNA and a primer targeting the vicinity of the peptidyl-transferase centre was used to determine cleavage sites at the nucleotide level. Results. We report here the mapping of putative cleavage sites within domains IV and V, enclosing the peptidyl transferase centre, in the 3'-half of the 23S rRNA molecule. Three cleavage sites were located in domain IV. Two other cleavage sites were located in the peptidyl transferase centre, and one presumptive multiple-break site between helices 77 and 78 in domain V. The DNA motifs were different from the postulated A + U rich single-strand cleavage sites recognised by RNase E, which has been implicated in rRNA degradation in Escherichia coli. Conclusions. The present analysis suggests that a hitherto unknown mechanism is responsible for the nonrandom fragmentation of rRNA in coccoid H. pylori, which may have important consequences for the growth, and survival of the bacterium.
653 a 23S rRNA cleavage sites
653 a Coccoid Helicobacter pylori
653 a Ds-cDNA primer extension
653 a MEDICINE
653 a MEDICIN
700a de la Cour, CD4 aut
700a Jonasson, Jon,d 1942-u Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Institutionen för hälsa och miljö,Klinisk mikrobiologi4 aut0 (Swepub:liu)jonjo59
710a Linköpings universitetb Hälsouniversitetet4 org
773t Helicobacterd : Wileyg 6:2, s. 100-109q 6:2<100-109x 1083-4389x 1523-5378
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-25978
8564 8u https://doi.org/10.1046/j.1523-5378.2001.00015.x

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de la Cour, CD
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Helicobacter
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Linköpings universitet

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