Difference between revisions of "Part:BBa K512001"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K512001 short</partinfo> | <partinfo>BBa_K512001 short</partinfo> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | casABCDE12 is a series of cas (CRISPR-associated) genes responsible for CRISPR interference in E. coli. These genes make up seven of the eight cas genes involved in the assembly of the Cascade (CRISPR-associated complex for antiviral defence) complex. This complex has been studied to provide immunity to viral infections and plasmid conjugation. casE, in particular, has been studied to be an endonuclease in ''E. coli'' that cleaves precursor CRISPR RNA into small crRNAs that bind with Cascade and guide the defense against foreign viruses and plasmids. | ||
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+ | Additional studies have shown that only cas genes casABCDE and cas3 are required for CRISPR interference to work. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K512001 SequenceAndFeatures</partinfo> | <partinfo>BBa_K512001 SequenceAndFeatures</partinfo> | ||
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<partinfo>BBa_K512001 parameters</partinfo> | <partinfo>BBa_K512001 parameters</partinfo> | ||
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+ | ===Source=== | ||
+ | casABCDE12 has been cloned from genomic DNA of DH5a. | ||
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+ | ===References=== | ||
+ | #Brouns, S.J.J., et. al. (2008) Small CRISPR RNAs guide antiviral defense in prokaryotes. ''Science'' '''321''': 960-964. | ||
+ | #Westra, E.R., et. al. (2010) H-NS-mediated repression of CRISPR-based immunity in ''Escherichia coli'' K12 can be relieved by the transcription activator LeuO. ''Molecular Microbiology'' '''77''':1380-1393. |
Revision as of 00:40, 29 September 2011
casABCDE12
Usage and Biology
casABCDE12 is a series of cas (CRISPR-associated) genes responsible for CRISPR interference in E. coli. These genes make up seven of the eight cas genes involved in the assembly of the Cascade (CRISPR-associated complex for antiviral defence) complex. This complex has been studied to provide immunity to viral infections and plasmid conjugation. casE, in particular, has been studied to be an endonuclease in E. coli that cleaves precursor CRISPR RNA into small crRNAs that bind with Cascade and guide the defense against foreign viruses and plasmids.
Additional studies have shown that only cas genes casABCDE and cas3 are required for CRISPR interference to work.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 84
Illegal PstI site found at 1253 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 84
Illegal PstI site found at 1253 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 3094
Illegal BglII site found at 4279
Illegal BamHI site found at 23
Illegal BamHI site found at 3224
Illegal BamHI site found at 3585
Illegal BamHI site found at 4482 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 84
Illegal PstI site found at 1253 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 84
Illegal PstI site found at 1253
Illegal NgoMIV site found at 5203
Illegal AgeI site found at 784 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1764
Source
casABCDE12 has been cloned from genomic DNA of DH5a.
References
- Brouns, S.J.J., et. al. (2008) Small CRISPR RNAs guide antiviral defense in prokaryotes. Science 321: 960-964.
- Westra, E.R., et. al. (2010) H-NS-mediated repression of CRISPR-based immunity in Escherichia coli K12 can be relieved by the transcription activator LeuO. Molecular Microbiology 77:1380-1393.