Difference between revisions of "Part:BBa K2440001"

 
Line 1: Line 1:
  
 
__NOTOC__
 
__NOTOC__
−
<partinfo>BBa_K2440001 short</partinfo>
+
<partinfo>BBa_K2440000 short</partinfo>
  
−
It is used to knock down miR-214 and miR-654.
+
Locker B is a miRNA locker with two different functional modules to target miR-214 and miR-654 at the same time.
  
−
<!-- Add more about the biology of this part here
 
 
===Usage and Biology===
 
===Usage and Biology===
  
−
<!-- -->
+
It is one of the experimental cases which were constructed to examine the scalability, reliability and efficiency of the Overlapped Oligo Assembly (OOA) method.
−
<span class='h3bb'>Sequence and Features</span>
+
 
 +
===Overlapped Oligo Assembly method===
 +
 
 +
In OOA method, modularized DNA parts is designed into the chemically synthesized DNA oligo, and overlapped 5’-overhangs are added for assembly. After that, dsDNAs can be obtained by annealing of two complementary single-strand oligonucleotides, then phosphorylated by T4 Polynucleotide Kinase to facilitate the following ligation reaction. T4 DNA ligase is use for their ligation onto pSB1C3 plasmid backbone. High-throughput one-step assemble of multiple short dsDNA nucleotides can therefore be achieved, and the correct assembling order is guaranteed by using identical overlap sequences among oligos, serving as zipcodes. The zipcodes are introduced as the intervals in a miRNA Locker.
 +
The dsDNA assembles are capable of being sub-cloned into plasmid backbones for amplification and long-term storage. In view of that, a prefix and a suffix is added to the dsDNA oligos forming the 5’ and 3’ terminus of the assembly, ensuring that the plasmids we constructed are compatible with BioBrick RFC[10].
 +
 
 +
[[File:NUDT-part-locker.jpeg|500px|]]
 +
 
 +
Figure 1. Schematic representation of the Overlapped Oligo Assembly method
 +
 
 +
===Sequence and Features===
 +
 
 
<partinfo>BBa_K2440001 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2440001 SequenceAndFeatures</partinfo>
  
 +
==Experimental Validation==
 +
 +
This part is validated through four ways: enzyme cutting, PCR, Sequence, and functional testing
 +
 +
===Sequencing===
 +
 +
This part is sequenced as correct after construction.
 +
 +
===PCR===
 +
 +
'''Methods'''
 +
 +
The PCR is performed with Premix EX Taq by Takara.
 +
 +
F-Prime: 5’- GAATTCGCGGCCGCTTCTAGAATGC-3’
 +
 +
R-Prime: 5’- GGACTAGTATTATTGTTTGTCTGCC-3’
 +
 +
The PCR protocol is selected based on the Users Manuel.
 +
The Electrophoresis was performed on a 1％ Agarose glu.
 +
The result of the agarose electrophoresis was shown on the picture below.
 +
 +
[[File:NUDT-part-lockerB.png|500px|]]
 +
 +
===Enzyme digestion test ===
 +
 +
'''Methods'''
 +
 +
After the assembly ,the plasmid was transferred into the Competent ''E. coli'' DH5α). After culturing overnight in LB,we minipreped the plasmid for cutting.
 +
The preparation of the plasmid was performed with TIANprep Mini Plasmid Kit from ''TIANGEN''. The cutting procedure was performed with EcoRI and SpeI restriction endonuclease bought from ''TAKARA''.
 +
 +
The plasmid was cutted in a 20μL system at 37 ℃ for 2 hours.
 +
The Electrophoresis was performed on a 1％ Agarose glu.
 +
 +
The result of the agarose electrophoresis was shown on the picture above.
  
−
<!-- Uncomment this to enable Functional Parameter display
+
===Functional Test===
−
===Functional Parameters===
+
−
<partinfo>BBa_K2440001 parameters</partinfo>
+
−
<!-- -->
+

Revision as of 19:39, 1 November 2017


Locker A

Locker B is a miRNA locker with two different functional modules to target miR-214 and miR-654 at the same time.

Usage and Biology

It is one of the experimental cases which were constructed to examine the scalability, reliability and efficiency of the Overlapped Oligo Assembly (OOA) method.

Overlapped Oligo Assembly method

In OOA method, modularized DNA parts is designed into the chemically synthesized DNA oligo, and overlapped 5’-overhangs are added for assembly. After that, dsDNAs can be obtained by annealing of two complementary single-strand oligonucleotides, then phosphorylated by T4 Polynucleotide Kinase to facilitate the following ligation reaction. T4 DNA ligase is use for their ligation onto pSB1C3 plasmid backbone. High-throughput one-step assemble of multiple short dsDNA nucleotides can therefore be achieved, and the correct assembling order is guaranteed by using identical overlap sequences among oligos, serving as zipcodes. The zipcodes are introduced as the intervals in a miRNA Locker. The dsDNA assembles are capable of being sub-cloned into plasmid backbones for amplification and long-term storage. In view of that, a prefix and a suffix is added to the dsDNA oligos forming the 5’ and 3’ terminus of the assembly, ensuring that the plasmids we constructed are compatible with BioBrick RFC[10].

NUDT-part-locker.jpeg

Figure 1. Schematic representation of the Overlapped Oligo Assembly method

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Experimental Validation

This part is validated through four ways: enzyme cutting, PCR, Sequence, and functional testing

Sequencing

This part is sequenced as correct after construction.

PCR

Methods

The PCR is performed with Premix EX Taq by Takara.

F-Prime: 5’- GAATTCGCGGCCGCTTCTAGAATGC-3’

R-Prime: 5’- GGACTAGTATTATTGTTTGTCTGCC-3’

The PCR protocol is selected based on the Users Manuel. The Electrophoresis was performed on a 1％ Agarose glu. The result of the agarose electrophoresis was shown on the picture below.

NUDT-part-lockerB.png

Enzyme digestion test

Methods

After the assembly ,the plasmid was transferred into the Competent E. coli DH5α). After culturing overnight in LB,we minipreped the plasmid for cutting. The preparation of the plasmid was performed with TIANprep Mini Plasmid Kit from TIANGEN. The cutting procedure was performed with EcoRI and SpeI restriction endonuclease bought from TAKARA.

The plasmid was cutted in a 20μL system at 37 ℃ for 2 hours. The Electrophoresis was performed on a 1％ Agarose glu.

The result of the agarose electrophoresis was shown on the picture above.

Functional Test