Difference between revisions of "Team:CSU CHINA/Notebook"
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<h4>2.Then we utilized these cDNA for qPCR </h4> | <h4>2.Then we utilized these cDNA for qPCR </h4> | ||
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<h4>1. We took the synthetic sequence(miR-141-BS and miR-148b-BS) for PCR amplification</h4> | <h4>1. We took the synthetic sequence(miR-141-BS and miR-148b-BS) for PCR amplification</h4> | ||
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<h4>3. We cut the fragments of gel and performed purification</h4> | <h4>3. We cut the fragments of gel and performed purification</h4> | ||
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<h4>1.We digested the two binding sites with the same incision enzyme with the vector (LSBr5and3), then we connected BS and vector together.</h4> | <h4>1.We digested the two binding sites with the same incision enzyme with the vector (LSBr5and3), then we connected BS and vector together.</h4> | ||
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<p>We transferred the bacteria cells to the solid LB medium with Amp<sup>+</sup></p> | <p>We transferred the bacteria cells to the solid LB medium with Amp<sup>+</sup></p> | ||
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<p>We purchased the primer of sponge of two miRNA: miR-141 and miR-148b</p> | <p>We purchased the primer of sponge of two miRNA: miR-141 and miR-148b</p> | ||
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<p>We got the primer and took up for PCR amplification</p> | <p>We got the primer and took up for PCR amplification</p> | ||
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<p>Then put the reaction system to the PCR machine</p> | <p>Then put the reaction system to the PCR machine</p> | ||
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<p>We designed the primer of the three synthetic promoters used for three Modules</p> | <p>We designed the primer of the three synthetic promoters used for three Modules</p> | ||
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<p>Golden gate method to connect the elements </p> | <p>Golden gate method to connect the elements </p> | ||
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<p>Then, we amplified them by PCR</p> | <p>Then, we amplified them by PCR</p> | ||
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<h4>1. pEGFP-N1-Module2(148b): pEGFP-N1-s(ESR1)p-(Sponge-148b) </h4> | <h4>1. pEGFP-N1-Module2(148b): pEGFP-N1-s(ESR1)p-(Sponge-148b) </h4> | ||
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<h4>2. pEGFP-N1-Module2(141): pEGFP-N1-s(ESR1)p-(Sponge-141) </h4> | <h4>2. pEGFP-N1-Module2(141): pEGFP-N1-s(ESR1)p-(Sponge-141) </h4> | ||
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<h4>3.PCR amplification</h4> | <h4>3.PCR amplification</h4> | ||
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<p>We turned to golden gate method to connect all the elements of Module1</p> | <p>We turned to golden gate method to connect all the elements of Module1</p> | ||
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<p> Then, we amplified them by PCR</p> | <p> Then, we amplified them by PCR</p> | ||
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Latest revision as of 17:09, 16 November 2019
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| 2019 | May | |||||
|---|---|---|---|---|---|---|
| SUN | MON | TUE | WED | THU | FRI | SAT |
NOTEBOOK
May
Main tasks
May 13-25
Screening TNBC specific Transcription factors (TFs)
May 27-29
Screening of low-expressed miRNA in TNBC
May 13
We screened for high-expressed genes in tumor groups in all invasive breast cancer from GEPIA database. Then, 245 genes is selected initially. 86 normal breast transcriptome samples and 303 tumor transcriptome samples were downloaded from TCGA (The Cancer Genome Atlas) database. The differentially expressed genes were screened by EdgeR algorithm. And all genes were selected in the GEPIA results set (245).
May 16
We used the GEPIA database to test the most specific differential-expressed gene in invasive breast cancer, and found out that 11 overlaps with the previously selected 245. Following the priority order for transcription factor identification, 9 transcription factors were identified.
May 21
Today we designed the primer of 9 TFs for PCR, and verified the expression of 9 selected TFs with qPCR.
May 22
Through RT reaction of mRNA and qPCR towards the cDNA, we got the results of qPCR. According to the expression in TNBC cell lines and normal cell lines, We chose ESR1 and GATA3 to design synthetic promoters.
May 25
We checked the potential specific miRNA in TNBC cells from articles and verified from TGCA database, then we purchased the primers of these miRNAs and amplified them The miRNAs we chose: miR-148b , miR-591, miR-125b, miR-34c-3p, miR-26a/26b, miR-216b, miR-101, miR-340, miR-409-3p, miR-489, miR-141, miR146a, miR-542-3p, miR-135a
May 27
1.We performed reverse transcription on miRNA and got these cDNA
| Step | Temperature | Time |
|---|---|---|
| Reverse transcription | 16℃ | 30min |
| 42℃ | 30min | |
| Stop reaction | 85℃ | 5min |
| Hold | 4℃ | Hold |
2.Then we utilized these cDNA for qPCR
| SYBR | 5μl |
| F Primer | 0.2μl |
| R Primer | 0.2μl |
| ddH2O | 2.6μl |
| cDNA | 2μl |
| Total | 10μl |
| Then put them for qPCR machine | |
| 95℃ for 10min | |
| 95℃ for 15s | 40 cycles |
| 60℃ for 60s | |
| 4℃ reserved | |
3.Result
May 29
We chose the specifically high-expressed miRNA: miR-148b and miR-141 for qPCR, and the result was showed below.
June
Main Tasks
June 3-10
Construction and examination of Binding Sites
June 3
We purchased the service of synthesizing the whole sequence for binding sites of miR-141 and miR-148b(then got the miR-141-BS and miR-148b-BS) from Sangon Biotech.
| Items | Sequence ( 5‘→3’) | Length |
|---|---|---|
| miR-141-BS | ATTGTGACTAGACCATTTCTAATGCCATTGTGACTAGACCATTTCTAATGCCATTGTGACTAGACCATTTCTAATGCCATTGTGACTAGACCATTTCTAATGGCAA | 106 |
| miR-148b-BS | ACAAAGTTCTGTGATGCACTGAATGCCACAAAGTTCTGTGATGCACTGAATGCCACAAAGTTCTGTGATGCACTGAATGCCACAAAGTTCTGTGATGCACTGAATGGCAA | 110 |
June 6
1. We took the synthetic sequence(miR-141-BS and miR-148b-BS) for PCR amplification
| Reagent | Volume(μl) |
|---|---|
| 5X Buffer | 10 |
| DMSO | 4 |
| dNTP | 4 |
| Forward Primer | 2 |
| Reverse Primer | 2 |
| Targeted DNA fragment | 1 |
| phusion | 1 |
| ddH2O | 26 |
| In Total | 50 |
| 95℃ for 10min | |
| 95℃ for 15s | n cycles |
| n℃ for 60s | |
| 4℃ reserved |
2. Then, we checked the result of PCR through agarose gel electrophoresis（1% agarose gel；110V for 30min）
3. We cut the fragments of gel and performed purification
| PCR production purification | |
|---|---|
| PE Buffer | 750μl/per column |
| PB Buffer | 50μl |
| Elution Buffer | 30μl |
| Gel recycling | |
| PE Buffer | 600μl |
| EB Buffer | 50μl |
Finally, we got the amplified products of miR-141-BS and miR-148b-BS and made them stored at -20℃
June 7
1.We digested the two binding sites with the same incision enzyme with the vector (LSBr5and3), then we connected BS and vector together.
| Digestion | DNA | Vector |
| In Total | 10 | 15 |
| Kpn11 | 1 | 1 |
| Xho1 | 1 | 1 |
| 10XBuffer | 2 | 2 |
| ddH2O | 6 | 11 |
| Connection | Volume | |
| Fragment | 3μl | |
| Vector | 10μl | |
| 10XBuffer | 2μl | |
| T4 DNA Ligase | 3μl | |
| ddH2O | 2μl | |
| Total | 20μl | |
2.We got the recombined plasmids to translate them to the competent E.coli cells
| PGL4.22-Promoter | 0ng | 5 ng | 10 ng | 20 ng |
| β-Gal(line lacZ) | 10ng | 10 ng | 10 ng | 10 ng |
| Empty | 90 ng | 85 ng | 80 ng | 70 ng |
| The total plasmid DNA content of each hole (12 holes in total) in the 24-well plate was 100ng.According to the Lipomax: DNA = 3 mu l;The 100ng ratio is configured with the following optin mixture | ||||
| +25μl Optin-DNA | Incubate 5min | |||
| +25μl Optin-Lipomax | incubate5min | |||
| Blend, then incubate for 20min（the system has a total of 50μl） | ||||
3.We cultured the bacteria cells with concussion for 12h
June 8
We transferred the bacteria cells to the solid LB medium with Amp+
| Solid LB medium with Amp+ | |
| LB medium （liquid） | 3.96ml |
| Amp | 4μl |
June 9
We picked up the AmpR+ cells and put miRNA mimics of miR-141 and miR-148b to the liquid medium
June 10
We took these cells for FACS gauging and observed the rate of different colors expressed by cells
July
Main Tasks
July 13-24
Construction of Sponge and gauging efficiency of Sponge
July 25-30
Construction of Synthetic Promoter and gauging efficiency of promoter (Partly, the rest was done in August)
July 13
We purchased the primer of sponge of two miRNA: miR-141 and miR-148b
| Items | Sequence(5’→3’) |
|---|---|
| F-miR-141-sponge | CGTCTCCAGCCGTAGAAGGA |
| R-miR-141-sponge | CGTCTCCCGAGCATCTTCCT |
| F-miR-148b-sponge | CGTCTCCAGCCACAAAGTTG |
| R-miR-148b-sponge | CGTCTCCCGAGTCAGTGCAT |
July 15
We got the primer and took up for PCR amplification
| Reagent | Volume(μl) |
|---|---|
| 5X Buffer | 10 |
| DMSO | 4 |
| dNTP | 4 |
| Forward Primer | 2 |
| Reverse Primer | 2 |
| Targeted DNA fragment | 1 |
| phusion | 1 |
| ddH2O | 26 |
| In Total | 50 |
Then put the reaction system to the PCR machine
| Cycle | Temperature | Time |
|---|---|---|
| 94℃ | 5min | |
| 10 cycles Add 0.5℃ after per cycle | 94℃ | 30s |
| 55℃ | 30s | |
| 72℃ | 30s | |
| 25 cycles | 94℃ | 30s |
| 60℃ | 30s | |
| 72℃ | 30s | |
| 72℃ | 7min | |
| 4℃ | reserved |
We took the products for agarose gel electrophoresis
We cut the fragments of gel and performed purification
Finally, we got the amplified products of Sponge-miR-141 and Sponge-miR-148b and stored at -20℃
July 16
We chose to construct the plasmid pEGFP-N1-sponge141_148b. Through double digestion towards the plasmid and the two Sponge, we made them connected and translated them to the competent E.coli cells
July 17
We gauged the efficiency of Sponge expression through luciferase assay
July 25
We designed the primer of the three synthetic promoters used for three Modules
| F-ESR1-EcoRI | CCGGAATTCATGACCATGACCCTCCAC |
| R-ESR1-BamHI | CGCGGATCCTCAGACCGTGGCAGGGAA |
| F-GATA3-EcoRI | CCGGAATTCATGGAGGTGACGGCGGAC |
| R-GATA3-BamHI | CGCGGATCCCTAACCCATGGCGGTGAC |
| R-G8p-XhoI | CCGCTCGAGTTTACCAACAGTACCGGA |
| R-lateADEp-XhoI | CCGCTCGAGAGAGTGAGGACGAACGCC |
| F-G8p-SacI | CGAGCTCCGATAGGTACCGAGTTTC |
| F-G8p-KpnI | CGGGGTACCCGATAGGTACCGAGTTTC |
July 28
We designed the structure of s(GATA3)p for Module1
Plasmid: PGL4.22-s(GATA3)p
July 30
We designed the structure of s(GATA3)p for Module1
Plasmid: PGL4.22-s(GATA3)p
August
Main Tasks
August 6-20
Golden Gate method for connection
August 24-30
Construction of Module1
August 2
We designed the structure of s(ESR1)p for Module3
Plasmid: pGL4.22-G8p
August 5
We tested the efficiency of promoters.
Plasmid: pGL4.22-hTERT
August 6
We utilized Golden gate method to connect Module1 and Module2
Plasmid: pEGFP-N1-lacZ
August 8
We constructed the plasmid for Module1
Promoter region: BsmBI RS-s(GATA3)p-BsmBI RS; screening and identification region: BsmBI RS-lacZp-lacZ-BsmBI RS
August 11
We constructed pLN431-s(GATA3)p
Golden gate method to connect the elements
| pLN431 plasmid | 2μl |
| s(GATA3)p | 1μl |
| 10XT4 Ligase Buffer | 2μl |
| 10XBuffer | 2μl |
| BsmBI | 1μl |
| ddH2O | 12l |
| Total | 20μl |
Then, we amplified them by PCR
| Step 1(X10) | |
|---|---|
| 37℃ | 5min |
| 16℃ | 10min |
| Step 2 | |
| 37℃ | 15min |
| 50℃ | 5min |
| 80℃ | 5min |
| Step 3 | |
| 16℃ | reserved |
August 12
We constructed the plasmid for Module2
August 16
1. pEGFP-N1-Module2(148b): pEGFP-N1-s(ESR1)p-(Sponge-148b)
| Vector | 2μl |
| miR141-Sponge | 1μl |
| s(ESR1)p | 1μl |
| 10XT4 Ligase Buffer | 2μl |
| 10XBuffer | 2μl |
| BsmBI | 1μl |
| ddH2O | 11μl |
| Total | 20μl |
2. pEGFP-N1-Module2(141): pEGFP-N1-s(ESR1)p-(Sponge-141)
| Vector | 2μl |
| miR141-Sponge | 1μl |
| s(ESR1)p | 1μl |
| 10XT4 Ligase Buffer | 2μl |
| 10XBuffer | 2μl |
| BsmBI | 1μl |
| ddH2O | 11μl |
| Total | 20μl |
3.PCR amplification
| Step 1(X10) | |
|---|---|
| 37℃ | 5min |
| 16℃ | 10min |
| Step 2 | |
| 37℃ | 15min |
| 50℃ | 5min |
| 80℃ | 5min |
| Step 3 | |
| 16℃ | reserved |
August 20
We tested the construction of Plasmid and important elements via gel electrophoresis
August 24
We got the sequences of elements of Module1
Here is the sequence of GAD
August 25
We turned to golden gate method to connect all the elements of Module1
| pLN431 plasmid | 2μl |
| s(GATA3)p | 1μl |
| 10XT4 Ligase Buffer | 2μl |
| 10XBuffer | 2μl |
| BsmBI | 1μl |
| ddH2O | 12l |
| Total | 20μl |
Then, we amplified them by PCR
| Step 1(X10) | |
|---|---|
| 37℃ | 5min |
| 16℃ | 10min |
| Step 2 | |
| 37℃ | 15min |
| 50℃ | 5min |
| 80℃ | 5min |
| Step 3 | |
| 16℃ | reserved |
September
Main tasks
September 2-11
Construction of Module3
September 13-20
Construction of Module2
September 21-29
III. Transfection with Transferrin modified liposome
September 2
| R-G8p-XhoI | CCGCTCGAGTTTACCAACAGTACCGGA |
| R-lateADEp-XhoI | CCGCTCGAGAGAGTGAGGACGAACGCC |
| SF-G8p-SacI | CGAGCTCCGATAGGTACCGAGTTTC |
| F-G8p-KpnI | CGGGGTACCCGATAGGTACCGAGTTTC |
September 5
Basic parts connecting
yCD
September 9
We constructed pLN431-G8p-yCD-(miR-BS)
September 11
We translated the plasmid to E.coli and transferred them to Amp+ solid medium , then picked the single bacterial colony for sequencing whether the plasmid was constructed correctly
September 13
We connected the elements of Module2 with Golden gate method and amplified.
1.Basic plasmid: pEGFP-N1-LacZ
2.Elements of Module2
PEGFP-N1- LacZ-s(ESR1)p Sponge
3.Connection by Golden gate method and constructing the whole Module2
We constructed pEGFP-N1-LacZ-miR148b-sponge; pEGFP-N1-LacZ-miR141-sponge; pEGFP-N1-LacZ-miR101-sponge
4.Amplification of Module2
| F-s(ESR1)p-BsmBI | GCCATCGTCTCCACTGAGGTCACGGTGACCT |
| R-s(ESR1)p-BsmBI | CGATTCGTCTCCGGCTAGAGTGAGGACGAA |
| F-miR141spe-EcoRI | CCGGAATTCGCCGTAGAAGGAATGTCA |
| R-miR141spe-BamHI | CGCGGATCCGAGCATCTTCCTTACAGT |
| F-miR148bspe-EcoRI | CCGGAATTCGCCACAAAGTTGTGAAAT |
| R-miR148bspe-BamHI | CGCGGATCCGAGTCAGTGCATTTCA |
| F-s(ESR1)p-KpnI | CGGGGTACCAGGTCACGGTGACCTTCT |
| Sponge-141-BsmBI | CGTCTCCAGCCGTAGAAGGAATGTCACAACCAGATAGACCAACACTGTAAGGAAGATGGATAGGTAGAAGGAATGTCACAACCAGATAGACCAACACTGTAAGGAAGATGGATAGGTAGAAGGAATGTCACAACCAGATAGACCAACACTGTAAGGAAGATGGATAGGTAGAAGGAATGTCACAACCAGATAGACCAACACTGTAAGGAAGATGCTCGGGAGACG |
| Sponge-148b-BsmBI | CGTCTCCAGCCACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTAGACAAAGTTGTGAAATGCACTGACTCGGGAGACG |
September 15
We translated the plasmid to E.coli and transferred them to Amp+ solid medium , then picked the single bacterial colony for sequencing whether the plasmid was constructed correctly
September 20
We tested when Module1+Module3 to examine whether G8p can be expressed.
September 21
We utilized the plasmid of Module1 2 3 for co-transfecting
September 24
HBL-100 with TF-NC for Day1
HBL-100 with TF-p53 for Day1
MDA-MB-231 with TF-NC for Day1
MDA-MB-231 with TF-p53 for Day1
September 2
HBL- 100 with TF-NC for Day2
HBL- 100 with TF-p53 for Day2
MDA-MB-231 with TF-NC for Day2
MDA-MB-231 with TF-p53 for Day2
DAPI Staining of MDA-MB-231 with TF-P53 For Day1
DAPI Staining of MDA-MB-231 with TF-P53 For Day2
October
Main Tasks
October 8-10
DAPI staining
October 8
We used DAPI staining method to observe the system that transfected to MBA-MD-231 and HBL-100 for one day to test whether it worked.
1.We prepared the two cell lines with transfecting the whole circuit, then operated as followed
- Wash the media with PBS for three times
- Incubate with PFA for 30-60 minutes
- Wash the media with PBS for three times
- Incubate in a solution of 1µg/ml 4,6-diamidino-2-phenylindole (DAPI) for 30 minutes
- Count cells under fluorescence microscope
2.Results
Fig.1 HBL-100 transfected with liposome for Day1
Fig.2 MDA-MB-231 transfected with liposome for Day1
October 9
We left the same cells as Octo.8 after being transfected for the two days , here were the results.
Fig.3 HBL-100 cell line with DAPI Staining under fluorescent microscope for Day2
Fig.4 MDA-MB-231 cell line with DAPI Staining under fluorescent microscope for Day2
October 10
We left the same cells as Oct.8 after being transfected for the three days , then we observed obvious results differentially in TNBC cells and normal cells.
Fig.5 HBL-100 cell line with DAPI Staining under fluorescent microscope for Day 3
Fig.6 MDA-MB-231 cell line with DAPI Staining under fluorescent microscope for Day3
Comparing Day2 and Day3, we noticed that the whole system transfected to MDA-MB-231 cells successfully worked and killed TNBC cells efficiently and specifically.