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From 2012hs.igem.org

Contents 1 Testing of DNA prepared by several methods 2 PCR of promoters and fluorescent protein coding sequences 3 Blunting the PCR Product 4 Digestion of pUC19 5 Ligation 6 Transformation 7 BsaI-digested Miniprep DNA 8 Obtaining the remaining clones

Testing of DNA prepared by several methods

Yeast genomic DNA is commonly prepared using a phenol/chloroform based method. Because both phenol and chloroform are toxic chemicals, we tested several methods for preparing yeast genomic DNA that do not use these chemicals. We compared a method that uses LiOAc to disrupt the yeast cell wall (BioTechniques 50:325-328, 2011) to methods that use the enzyme zymolyase to disrupt the cell wall (a Promega kit or a [http://www.bio.brandeis.edu/haberlab/jehsite/pdfs/ZymoPrep.pdf protocol from Jim Haber’s lab], “JH zym”). For the Haber lab protocol, we did not include beta mercaptoethanol in the zymolyase solution, realizing that without this the zymolyase step might take longer. We used the procedure in the Haber lab protocol to check the completion of the zymolyase digestion for the Promega protocol and the Haber lab protocol. DNA from all protocols was treated with RNase A. The Haber lab protocol produced the greatest yield of genomic DNA, but DNA made using the Promega kit was used in subsequent PCRs because it seemed to produce the most consistent results. 1µl, 2µl, or 5µl of genomic DNA was used in each PCR reaction with LIF1 promoter primers. The exception was that the DNA prepared using the Haber lab protocol was diluted 1:10 because it was about 10X more concentrated than the DNA prepared using the other methods. Following these initial tests, 1µl of yeast genomic DNA was used for subsequent PCRs. The LiOAc method was the shortest and least expensive and we may switch to this method when future DNA preps for PCR are needed. It should be noted that in retrospect, the PCR reactions below were too robust to fairly compare the DNA preps. DNA would need to be diluted and/or the cycles would need to be shortened to come close to having PCR reactions in the linear range. However, we learned from this that we had successfully prepared genomic DNA, so we moved forward.

For PCR, we used:

Yeast Genomic DNA: 1µl or 2µl or 5µl

2X OneTaq Mix (NEB): 25µl

5µM Forward primer: 2.5µl

5µM Reverse primer: 2.5µl

H2O: 19µl or 18µl or 15µl

Cycling conditions

1 cycle of:

94°C 5 min

15 cycles of:

94°C 30 sec

50°C 30 sec

68°C 45 sec

30 cycles of:

94°C 30 sec

55°C 30 sec

68°C 45 sec

1 cycle of:

68°C 5 min

PCR of promoters and fluorescent protein coding sequences

We did an isolation of genomic DNA from yeast using the Promega Wizard Genomic DNA Purification Kit- cat# A1120. We substituted 20T zymolyase (Seikagaku) for lyticase.

For PCR, we used:

Yeast Genomic DNA: 1µl

2X OneTaq Mix (NEB): 25µl

5µM Forward primer: 2.5µl

5µM Reverse primer: 2.5µl

H2O: 19µl

Cycling conditions

1 cycle of:

94°C 5 min

15 cycles of:

94°C 30 sec

50°C 30 sec

68°C 45 sec

30 cycles of:

94°C 30 sec

55°C 30 sec

68°C 45 sec

1 cycle of:

68°C 5 min

The ladder on all gels is the 2-log ladder (NEB).

2% agarose gels in 1X Sodium Borate buffer: BioTechniques 36:214-216 (February 2004)

There may be more nonspecific bands in these PCR reactions than is typical either because there was a considerable delay waiting for all students to be ready to add their tubes to the PCR machine or because we had an issue where the program was initially incorrect and we needed to restart the PCR machine after correcting the problem.

Then we conducted a gel extraction, using QIAquick Gel Extraction Kit.

Blunting the PCR Product

After we had the purified PCR product, we used the Blunt Cloning Kit (NEB) to blunt and phosphorylate the ends of the PCR product. The blunting reaction was composed of:

Purified DNA: 15µl

10X Blunting Buffer: 2.5µl

1 mM dNTP Mix: 2.5µl

Blunt Enzyme Mix: 1.0µl

Sterile dH20: 4µl

Total Volume: 25µl

Digestion of pUC19

The pUC19 vector was digested with SmaI:

1µg/µl pUC19 (NEB): 5µl

10X NEBuffer 4: 3µl

SmaI: 1 µl

H2O: 11 µl

The restriction digest was incubated for 4 hours at 25°C. 1µl of Calf Intestinal Phosphatase (NEB) was added and the mixture was incubated at 37°C for 2 hrs.

Ligation

Next, we did a ligation reaction with the Quick Ligation Kit (NEB). We followed the manufacturer's suggested protocol which was to use a 3:1 molar ratio of insert: vector and 50 ng of SmaI digested/CIP'd pUC19 vector.

Transformation

For the transformation, we used NEB 10-beta Competent E. coli cells (cat # C3019H). We followed the manufacturer's suggested protocol for the transformation, and we plated on Ampicillin/IPTG/X-Gal.

BsaI-digested Miniprep DNA

Overall, most plates contained a mixture of blue and white colonies and the number of colonies was fairly low - not much higher than for our "no insert" ligations. We then picked two white colonies from each plate and inoculated 2ml of LB/amp and then mini-prepped the DNA. Blue colonies had intact lacZ genes, and therefore did not contain inserts. The samples on these gels contain BsaI-digested miniprep DNA prepared from individual colonies from the transformations above.

For the BsaI Digest, we used:

Miniprep DNA: 4µl

10X NEB4: 2µl

100X BSA: .2µl

BsaI: .5µl

H20: 13.3µl

Expected band sizes from BsaI digests

pUC19 (no insert): 1 cut, 1 band: 2686 bp

pUC19 + insert: 3 cuts, 3 bands: 1354 bp, 1332 bp, insert (expected sizes listed on gel below) Almost all inserts are a single BsaI fragment, but there is an internal BsaI site in the TEF1, ENO1, EAF6, and MSN4 promoters so 2 band sizes are listed for these inserts.

Note that the 1354bp and 1332bp bands will appear to run as one band on the gel.

Based on the data above, we concluded that the following clones had inserts of the correct size:

Promoters

MET15 yes: B

GAL1 yes: A

GAL1-L yes: A

GAL1-S yes: B

RAD52 yes: B

RAD50 yes: A

RAD54 yes: A, B

RAD55 yes: A, B

MRE11 yes: A, B

XRS2 yes: A, B

REV1 yes: B

TDH3 yes: A, B

LIF1 none

MIG1 yes: B

TUB1 yes: A

CSE4 yes: B

CLN2 yes: B

CLB2 none

ACT1 none

ENO1 yes: A (we initially forgot there should be 2 insert bands and so continued to try to get clones in the next steps)

ENO2 none

TEF2 yes: B

TEF1 none

EAF6 none (possibly a band, but too little DNA to be confident)

HSP12 yes: A, B

HSP26 yes: A

HSC82 none

MSN2 yes: A

MSN4 none

HHO1 yes: A, D

Protein-coding sequences

BFP maybe: A (the insert may be too large)

GFP none

YFP none

mTangerine none

mCherry yes: A (but bottom band seems possibly too intense)

mGrape1 none

Extra colonies were picked from the transformations for the following promoter clones:

LIF1, CLB2, ACT1, ENO1, ENO2, TEF1, EAF6, HSC82, MSN4

DNA from these clones was miniprepped using Qiagen minipreps. The DNA was digested with BsaI as follows:

miniprep DNA: 3µl

10X NEBuffer 4: 2µl

100X BSA: 0.2µl

BsaI: 0.5µl

H2O: 14.8µl

BsaI digests were incubated at 37°C for 2 hrs and then run on a 2% agarose gel in 1X sodium borate buffer.

Based on the data above, we concluded that the following clones had inserts of the correct size:

Promoters

LIF1 none

CLB2 yes: C

ACT1 yes: C

ENO1 none

ENO2 yes: C

TEF1 none

EAF6 yes: D (This was started from culture EAF6-B)

HSC82 none

MSN4 yes: C (we initially forgot there should be 2 insert bands and so continued to try to get clones in the next steps)

Obtaining the remaining clones

Because there had been relatively few colonies on most of the transformation plates, we decided to try 2 different strategies for obtaining the remaining clones:

1. Repeat the original blunt ligations using a higher insert:vector ratio. 2. Try a sticky-end ligation strategy since it may have a higher success rate than the blunt ligation strategy. (This strategy is outlined in detail below:

When we designed the PCR primers, we added nucleotides 5' to the BSA recognition site in both the forward and reverse primers. We decided to introduce the sequence 5' CCCGGG 3'which is the site for both SmaI (creates blunt ends) and XmaI (creates sticky ends). According to the NEB catalog, SmaI and XmaI can cut very close to the end of a PCR product. Thus, the introduction served as a backup strategy if the blunt cloning was problematic. The PCR products could be cut with XmaI and ligated into XmaI-digested pUC19.

The original PCR reaction was digested with XmaI for the following promoters:

LIF1, ENO1, TEF1, HSC82, MSN4

purified PCR product: 15µl

10X NEBuffer 4: 3µl

100X BSA: 0.3µl

XmaI: 0.5µl

H2O: 11.2µl

These digested PCR products were run on the gel below:

2% agarose gel in 1X sodium borate buffer:

These bands were excised and purified using the QiaQuick Gel Extraction Kit.

Because the cloning of the fluorescent proteins was particularly problematic, we repeated the PCR of these genes:

5ng/µl fluorescent protein vector: 2µl

2X OneTaq Mix (NEB): 25µl

5µM Forward primer: 2.5µl

5µM Reverse primer: 2.5µl

H2O: 18µl

Cycling conditions

1 cycle of:

94°C 5 min

15 cycles of:

94°C 30 sec

50°C 30 sec

68°C 45 sec

30 cycles of:

94°C 30 sec

55°C 30 sec

68°C 45 sec

1 cycle of:

68°C 5 min

PCR products were purified using the QiaQuick Gel Extraction Kit.

The purified PCR products were then digested with XmaI:

purified PCR product: 15µl

10X NEBuffer 4: 3µl

100X BSA: 0.3µl

XmaI: 0.5µl

H2O: 11.2µl

These digested PCR products were run on the gel below and the bands were excised and purified using the QiaQuick Gel Extraction Kit.

The pUC19 vector was digested with XmaI:

1µg/µl pUC19 (NEB): 5µl

10X NEBuffer 4: 3µl

100X BSA: 0.3µl

XmaI: 0.5µl

H2O: 11.2µl

The pUC19 vector was digested overnight at 37°C. Then, the reaction was heated at 65°C for 20min. 1µl of Calf Intestinal Phosphatase (NEB) was added to the reaction and it was incubated at 37°C for 2 hrs. This digested, dephosphorylated vector was run on the agarose gel below.

2% agarose gel in 1X sodium borate buffer:

These bands were excised and purified using the QiaQuick Gel Extraction Kit.

Strategy 1: blunted PCR products were ligated into SmaI/CIP'd pUC19 vector as before, except that a 10:1 molar insert:vector ratio was used.

Strategy 2: XmaI-digested PCR products were ligated into XmaI/CIP'd pUC19 vector using a 6:1 molar insert:vector ratio.

5µl of ligation reaction were transformed and plated on LB/Amp/X-gal/IPTG.

After about 18hrs, the plates with promoter clones had normal-sized colonies, but the colonies on the plates for the fluorescent protein coding sequences were just barely visible. We realized in retrospect that we probably shouldn't have plated the cells for the fluorescent protein sequences on IPTG/X-gal plates. The IPTG induced transcription of B-galactosidase with the fluorescent protein insertion. We know from previous experience with fluorescent protein plasmids that these proteins are somewhat toxic. The toxicity of the fluorescent proteins could explain the small size of the colonies. We would suggest not using blue/white selection for future cloning of protein-coding sequences. These fluorescent protein plates were allowed to grow 2 more days at room temperature before colonies were picked (2 days because we couldn't access the school building on a Sunday). We picked 2 colonies from each plate into LB/amp and miniprepped the DNA. Several of the colonies that we picked from the blunt cloning plates for the fluorescent proteins failed to grow in LB/amp.

miniprep DNA: 3µl

10X NEBuffer 4: 2µl

100X BSA: 0.2µl

BsaI: 0.2µl

H2O: 14.6µl

BsaI digests were incubated at 37°C overnight and then run on a 2% agarose gel (promoters) or 1% agarose gel (fluorescent protein coding sequences) in 1X sodium borate buffer.

Based on the data above, we concluded that the following clones had inserts of the correct size:

Promoters

LIF1 yes: X2

ENO1 yes: X1,X2,B1,B2

TEF1 yes: X1,X2,B1

HSC82 yes: X1,X2,B1,B2

MSN4 yes: X2,B1,B2

Protein-coding sequences

BFP yes: X1,X2

GFP yes: X1,X2

YFP yes: X1,X2

mTangerine yes: X1,X2, B2

mCherry yes: X2

mGrape1 yes: X1,X2

NOW WE HAVE ALL THE CLONES!!!

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