Difference between revisions of "Part:BBa K2429063"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K2429063 short</partinfo> | ||
+ | Parts K2429063 through K2429068 and parts K2429083 through K2429093 are a family of guide sequences used by either a dCas13a variant or Ms2 to target the intron of the mKate FF4 reporters (BBa_K2429033 and BBa_K2429049). These guides lie downstream of a U6 promoter, which is a constitutive promoter typically used for the production of guide RNA. | ||
+ | Our team used multiple guide sequences to "tile" along the reporter’s intron to determine what part of the intron is best to target when trying to control its splicing efficiency. Based on the level of fluorescence associated with each guide, we can compare the results to see whether a specific targeted sequence is integral in the process of splicing, and whether the binding of the RNA binding protein to said sequence changes the splicing efficiency. | ||
+ | |||
+ | https://static.igem.org/mediawiki/2017/9/97/Tiling.PNG | ||
+ | |||
+ | The guides shift by a few base pairs so we can make more precise conclusions about what intronic sequences are important for splicing. | ||
+ | |||
+ | |||
+ | Parts K-63 through K-68 lead to guide RNA sequences that serve as a guide for the dCas13a protein. | ||
+ | |||
+ | https://static.igem.org/mediawiki/parts/b/bd/Lsh_FF4_guides.png | ||
+ | |||
+ | |||
+ | Parts K-83 through K-87 as well as K-93 lead to the production of antisense oligonucleotides (ASOs). Parts K-88 through K-92 consist of the same ASO sequences corresponding to the same order (i.e. K-83 sequence is used in K-88); however, they have an additional portion of nucleotides that will form a hairpin loop which Ms2 can bind. The addition of oligonucleotides without hairpins loops serves as a control to test whether it’s the guide sequence or the protein that is actually affecting splicing. | ||
+ | |||
+ | https://static.igem.org/mediawiki/parts/e/e1/ASO_FF4_guides.png | ||
+ | |||
+ | |||
+ | <!-- Add more about the biology of this part here | ||
+ | ===Usage and Biology=== | ||
+ | |||
+ | <!-- --> | ||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K2429039 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K2429039 parameters</partinfo> | ||
+ | <!-- --> |
Revision as of 18:12, 25 October 2017
mKate FF4 Guide Family Member Parts K2429063 through K2429068 and parts K2429083 through K2429093 are a family of guide sequences used by either a dCas13a variant or Ms2 to target the intron of the mKate FF4 reporters (BBa_K2429033 and BBa_K2429049). These guides lie downstream of a U6 promoter, which is a constitutive promoter typically used for the production of guide RNA.
Our team used multiple guide sequences to "tile" along the reporter’s intron to determine what part of the intron is best to target when trying to control its splicing efficiency. Based on the level of fluorescence associated with each guide, we can compare the results to see whether a specific targeted sequence is integral in the process of splicing, and whether the binding of the RNA binding protein to said sequence changes the splicing efficiency.
The guides shift by a few base pairs so we can make more precise conclusions about what intronic sequences are important for splicing.
Parts K-63 through K-68 lead to guide RNA sequences that serve as a guide for the dCas13a protein.
Parts K-83 through K-87 as well as K-93 lead to the production of antisense oligonucleotides (ASOs). Parts K-88 through K-92 consist of the same ASO sequences corresponding to the same order (i.e. K-83 sequence is used in K-88); however, they have an additional portion of nucleotides that will form a hairpin loop which Ms2 can bind. The addition of oligonucleotides without hairpins loops serves as a control to test whether it’s the guide sequence or the protein that is actually affecting splicing.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 4697
Illegal XbaI site found at 30
Illegal PstI site found at 2205
Illegal PstI site found at 2574
Illegal PstI site found at 3303 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 4697
Illegal PstI site found at 2205
Illegal PstI site found at 2574
Illegal PstI site found at 3303 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 4697
Illegal BglII site found at 949
Illegal BglII site found at 1573
Illegal BglII site found at 1969
Illegal BglII site found at 2260
Illegal BglII site found at 2350
Illegal BglII site found at 3511
Illegal BglII site found at 3598
Illegal BamHI site found at 339
Illegal BamHI site found at 4593 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 4697
Illegal XbaI site found at 30
Illegal PstI site found at 2205
Illegal PstI site found at 2574
Illegal PstI site found at 3303 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 6
Illegal EcoRI site found at 322
Illegal EcoRI site found at 4697
Illegal XbaI site found at 30
Illegal PstI site found at 2205
Illegal PstI site found at 2574
Illegal PstI site found at 3303
Illegal NgoMIV site found at 4550
Illegal NgoMIV site found at 4569 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 935
Illegal SapI.rc site found at 1041
Illegal SapI.rc site found at 1911
Illegal SapI.rc site found at 2745