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Identification and characterization of E. coli CRISPR‐cas promoters and their silencing by H‐NS
Abstract
Summary: Inheritable bacterial defence systems against phage infection and foreign DNA, termed CRISPR (c lustered r egularly i nterspaced s hort p alindromic r epeats), consist of cas protein genes and repeat arrays interspaced with sequences originating from invaders. The Cas proteins together with processed small spacer‐repeat transcripts (crRNAs) cause degradation of penetrated foreign DNA by unknown mechanisms. Here, we have characterized previously unidentified promoters of the Escherichia coli CRISPR arrays and cas protein genes. Transcription of precursor crRNA is directed by a promoter located within the CRISPR leader. A second promoter, directing cas gene transcription, is located upstream of the genes encoding proteins of the Cascade complex. Furthermore, we demonstrate that the DNA‐binding protein H‐NS is involved in silencing the CRISPR‐cas promoters, resulting in cryptic Cas protein expression. Our results demonstrate an active involvement of H‐NS in the induction of the CRISPR‐cas system and suggest a potential link between two prokaryotic defence systems against foreign DNA.
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Leader sequences have a length of approximately 500 bp, stand upstream of CRISPR loci, and carry promoter elements and signals for CRISPR systems adaptation that are crucial to crRNA transcription and the successful integration of foreign genetic material into CRISPR sequences.
“These leader sequences have a length of approximately 500 bp and carry promoter elements and signals for CRISPR systems adaptation that are crucial to the transcription of crRNA (CRISPR RNA) and the successful integration of foreign genetic material into CRISPR sequences [11,12].”
From CRISPR-Cas: Converting A Bacterial Defence Mechanism into A State-of-the-Art Genetic Manipulation Tool (2019) · cites this paper as [11]
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Research works printed but not linked: 69
- 10.1046/j.1365-2958.1998.00829.x · DOI
- 10.1128/JB.184.15.4168-4176.2002 · DOI
- 10.1126/science.1138140 · DOI · Paper page
- 10.1099/mic.0.28048-0 · DOI · Paper page
- 10.1006/prep.1993.1066 · DOI
- 10.1038/nsmb1233 · DOI
- 10.1128/jb.173.5.1789-1800.1991 · DOI
- 10.1016/0378-1119(84)90136-7 · DOI
- 10.1126/science.1159689 · DOI · Paper page
- 10.1021/bi00692a011 · DOI
- 10.1101/gad.1742908 · DOI
- 10.1038/nbt.1582 · DOI
- 10.1074/jbc.C100603200 · DOI
- 10.1111/j.1365-2958.1993.tb01634.x · DOI
- 10.1128/JB.01412-07 · DOI
- 10.1128/JB.186.9.2708-2716.2004 · DOI
- 10.1038/nrmicro1598 · DOI
- 10.1016/S0065-2164(08)01002-2 · DOI
- 10.1126/science.1137550 · DOI
- 10.1128/jb.175.22.7160-7169.1993 · DOI
- 10.1093/emboj/19.24.6697 · DOI
- Free A., 1998, The StpA protein functions as a molecular adapter to mediate repression of the bgl operon by truncated H‐NS in Escherichia coli, J Bacteriol, 180, 994, 10.1128/JB.180.4.994-997.1998 · DOI
- 10.1007/s00239-005-0223-z · DOI
- 10.1016/0003-9861(77)90521-5 · DOI
- 10.1261/rna.1246808 · DOI
- 10.1016/j.cell.2009.07.040 · DOI · Paper page
- 10.1046/j.1365-2958.2001.02358.x · DOI
- 10.1128/JB.01415-07 · DOI
- 10.1046/j.1365-2958.2002.02839.x · DOI · Paper page
- 10.1073/pnas.85.12.4237 · DOI
- 10.1093/nar/gkm712 · DOI
- 10.1093/emboj/20.5.990 · DOI
- 10.1155/2006/542818 · DOI
- 10.1111/j.1365-2958.2009.06641.x · DOI
- 10.1111/j.1365-2958.2007.05950.x · DOI
- 10.1073/pnas.90.5.1761 · DOI
- 10.1016/j.jsb.2006.05.006 · DOI
- 10.1093/nar/30.2.482 · DOI · Paper page
- 10.1186/1745-6150-1-7 · DOI · Paper page
- 10.1007/s00239-004-0046-3 · DOI · Paper page
- 10.1099/mic.0.023960-0 · DOI · Paper page
- 10.1093/nar/gkg037 · DOI
- 10.1101/gad.1543107 · DOI
- 10.1101/gad.1428206 · DOI
- 10.1016/j.tibs.2009.05.002 · DOI
- 10.1093/emboj/17.12.3439 · DOI
- 10.1073/pnas.91.5.1721 · DOI
- 10.1074/jbc.M709843200 · DOI
- 10.1074/jbc.M204268200 · DOI
- 10.1111/j.1365-2958.2005.04873.x · DOI
- 10.1016/j.jmb.2006.11.067 · DOI
- 10.1099/mic.0.2008/018408-0 · DOI
- 10.1046/j.1365-2958.1998.00720.x · DOI
- 10.1006/jmbi.2000.3708 · DOI
- 10.1074/jbc.M109.044313 · DOI
- 10.1128/JB.00108-09 · DOI
- 10.1038/nrmicro1793 · DOI
- 10.1099/mic.0.2008/020693-0 · DOI
- Stratmann T., 2007, Regulation of the yjjQ‐bglJ operon encoding LuxR‐type transcription factors and the divergent yjjP gene by H‐NS and LeuO, J Bacteriol, 190, 926, 10.1128/JB.01447-07 · DOI
- Studier F.W., 2009, Understanding the differences between genome sequences of Escherichia coli B strains REL606 and BL21(DE3) and comparison of the E. coli B and K‐12 genomes, J Mol Biol, 394, 635, 10.1016/j.jmb.2009.09.021 · DOI
- 10.1073/pnas.90.8.3511 · DOI
- 10.1016/S0076-6879(96)74023-5 · DOI
- 10.1006/jmbi.1996.0566 · DOI
- 10.1128/JB.01594-08 · DOI
- 10.1038/nsmb1130 · DOI
- 10.1016/j.cell.2009.01.043 · DOI
- 10.1016/j.jmb.2003.11.004 · DOI
- 10.1093/nar/20.24.6735 · DOI
- 10.1002/j.1460-2075.1996.tb00476.x · DOI
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Metadata
- Authors
- Pul, Ü., Wurm, R., Arslan, Z., Geißen, R., Hofmann, N., & Wagner, R.
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 2010-03
- Volume
- 75
- Issue
- 6
- Pages
- 1495-1512
- ISSN
- 0950-382X
- 1365-2958
- Cited by
- 282
- References
- 0
- Language
- en
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