CRISPR families of the crenarchaeal genus Sulfolobus: bidirectional transcription and dynamic properties
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CRISPR families of the crenarchaeal genus Sulfolobus: bidirectional transcription and dynamic properties. / Lillestøl, Reidun K; Shah, Shiraz Ali; Brügger, Kim; Redder, Peter; Phan, Hien; Christiansen, Jan; Garrett, Roger A.
In: Molecular Microbiology, Vol. 72, No. 1, 2009, p. 259-272.Research output: Contribution to journal › Journal article › Research › peer-review
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T1 - CRISPR families of the crenarchaeal genus Sulfolobus: bidirectional transcription and dynamic properties
AU - Lillestøl, Reidun K
AU - Shah, Shiraz Ali
AU - Brügger, Kim
AU - Redder, Peter
AU - Phan, Hien
AU - Christiansen, Jan
AU - Garrett, Roger A
PY - 2009
Y1 - 2009
N2 - Summary CRISPRs of Sulfolobus fall into three main families based on their repeats, leader regions, associated cas genes, and putative recognition sequences on viruses and plasmids. Spacer sequence matches to different viruses and plasmids of the Sulfolobales revealed some bias particularly for family III CRISPRs. Transcription occurs on both strands of the five repeat-clusters of Sulfolobus acidocaldarius and a repeat-cluster of the conjugative plasmid pKEF9. Leader strand transcripts cover whole repeat-clusters and are processed mainly from the 3'-end, within repeats, yielding heterogeneous 40 - 45 nt spacer RNAs. Processing of the pKEF9 leader transcript occurred partially in spacers, and was incomplete, probably reflecting defective repeat recognition by host enzymes. A similar level of transcripts was generated from complementary strands of each chromosomal repeat-cluster and they were processed to yield discrete approximately 55 nt spacer RNAs. Analysis of the partially identical repeat-clusters of Sulfolobus solfataricus strains P1 and P2 revealed that spacer-repeat units are added upstream only when a leader and certain cas genes are linked. Downstream ends of the repeat-clusters are conserved such that deletions and recombination events occur internally.
AB - Summary CRISPRs of Sulfolobus fall into three main families based on their repeats, leader regions, associated cas genes, and putative recognition sequences on viruses and plasmids. Spacer sequence matches to different viruses and plasmids of the Sulfolobales revealed some bias particularly for family III CRISPRs. Transcription occurs on both strands of the five repeat-clusters of Sulfolobus acidocaldarius and a repeat-cluster of the conjugative plasmid pKEF9. Leader strand transcripts cover whole repeat-clusters and are processed mainly from the 3'-end, within repeats, yielding heterogeneous 40 - 45 nt spacer RNAs. Processing of the pKEF9 leader transcript occurred partially in spacers, and was incomplete, probably reflecting defective repeat recognition by host enzymes. A similar level of transcripts was generated from complementary strands of each chromosomal repeat-cluster and they were processed to yield discrete approximately 55 nt spacer RNAs. Analysis of the partially identical repeat-clusters of Sulfolobus solfataricus strains P1 and P2 revealed that spacer-repeat units are added upstream only when a leader and certain cas genes are linked. Downstream ends of the repeat-clusters are conserved such that deletions and recombination events occur internally.
U2 - 10.1111/j.1365-2958.2009.06641.x
DO - 10.1111/j.1365-2958.2009.06641.x
M3 - Journal article
C2 - 19239620
VL - 72
SP - 259
EP - 272
JO - Molecular Microbiology
JF - Molecular Microbiology
SN - 0950-382X
IS - 1
ER -
ID: 11368650