Sam:LabNotes/Human-Chip-bisulfite-Seq/2010-2-27: Difference between revisions
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='''Low-Input DNA | ='''Low-Input DNA library construction - Internal marker templates test-2'''= | ||
==Background== | ==Background== | ||
*Repeat the low-input DNA | *Repeat the low-input DNA library construction with following changes: | ||
**Add inactivation step following End- | **Add inactivation step following End-repairing. | ||
**Try two more conditions of De-P-Carriers (carriers made by SAP 60min or ACP 60min) | **Try two more conditions of De-P-Carriers (carriers made by SAP 60min or ACP 60min) | ||
**Change the order of size-selection. '''The size-selection will be performed prior PCR amplification.''' | **Change the order of size-selection. '''The size-selection will be performed prior PCR amplification.''' | ||
== | ==Procedures== | ||
*Prepare the following samples | *Prepare the following samples | ||
**E.coli internal marker (IM) (200bp): 43.6ng/uL | **E.coli internal marker (IM) (200bp): 43.6ng/uL | ||
Line 26: | Line 26: | ||
'''NOTE: reactions B1, B2 and B3 will be added with De-P-carrier. Reactions B4 - B8 won't.''' | '''NOTE: reactions B1, B2 and B3 will be added with De-P-carrier. Reactions B4 - B8 won't.''' | ||
*Purify the DAN mixture with EtOH precipitation | *Purify the DAN mixture with EtOH precipitation | ||
**mimic the real | **mimic the real procedures to remove the enzyme and buffers from WGA reactions | ||
*Each sample (PCR product) has 100uL volume. Air dry the pellet. Dissolve the pellet in 34uL H2O. | *Each sample (PCR product) has 100uL volume. Air dry the pellet. Dissolve the pellet in 34uL H2O. | ||
===End- | ===End-repairing & Phosphorylation=== | ||
*End-it Kit (EPICENTRE) | *End-it Kit (EPICENTRE) | ||
Line 120: | Line 120: | ||
**Ladder well: 0.5uL low mass ladder + 3uL 6X loading dye + 6uL 0.5X TBE buffer | **Ladder well: 0.5uL low mass ladder + 3uL 6X loading dye + 6uL 0.5X TBE buffer | ||
[[File:sam030210-PCR amplified lib - 8th cycle.JPG|320px]] [[File:sam030210-PCR amplified lib - 12th cycle.JPG|300px]] | [[File:sam030210-PCR amplified lib - 8th cycle.JPG|320px]] [[File:sam030210-PCR amplified lib - 12th cycle.JPG|300px]] | ||
*'''The library from B5 didn't showed up in 8th cycle due to the insufficinet amplification'''. | |||
B1 B2 B3 B4 B5 B6''' | B1 B2 B3 B4 B5 B6''' | ||
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Sample (E.coli) 200bp ~300bp | Sample (E.coli) 200bp ~300bp | ||
Carrier (Lambda) 100bp ~200bp | Carrier (Lambda) 100bp ~200bp | ||
==Discussion== | ==Discussion== | ||
* | *'''Regardless which enzyme or condition was used, all dephosphorylated carriers are still ligated with adaptor in this test'''. | ||
**Sol1: Adjust the dephosphorylation conditions. | **Even I add the inactivation step (70C 10min)following End-repairing step, the situation was not imporved. | ||
**B4-B6: De-P-Carrier prepared by SAP, 30min. | |||
**B5: De-P-Carrier prepared by SAP, 60min. | |||
**B6: De-P-Carrier prepared by ACP, 60min. | |||
*Possible reasons of the appearance of adaptor-ligated carrier: | |||
**The Dephosphorylation is not complete. | |||
**The De-P-Carriere was rephosphorylated after End-repairing. | |||
**The Phosphorylation "on templates (insert)" is not playing the critical roll for ligation. | |||
*The method in this test (size selection prior PCR amplification) is still able to construct the library with only 10ng DNA (for both with or without carrier conditions). | |||
*The early size selection method can generate the libraries with much lower unspecific amplification. | |||
treated Regardless which enzyme or conditino were uuAll of Sol1: Adjust the dephosphorylation conditions. | |||
**Sol2: Add heat inactivation stet right after End-reparing reaction. | **Sol2: Add heat inactivation stet right after End-reparing reaction. | ||
*The smear (unspecific amplification) is weaker in those samples with lambda DNA carriers. Perhaps the Y-adaptor were comsumed more in those samples. | *The smear (unspecific amplification) is weaker in those samples with lambda DNA carriers. Perhaps the Y-adaptor were comsumed more in those samples. | ||
**'''I assumed that the overdose of Y-adaptor might be associated with the unspecific amplification.''' | **'''I assumed that the overdose of Y-adaptor might be associated with the unspecific amplification.''' | ||
*In the no lambda carries samples, even the 10ng input-DNA could be successfully made to library using the current protocl. | *In the no lambda carries samples, even the 10ng input-DNA could be successfully made to library using the current protocl. |
Revision as of 06:00, 3 March 2010
Low-Input DNA library construction - Internal marker templates test-2
Background
- Repeat the low-input DNA library construction with following changes:
- Add inactivation step following End-repairing.
- Try two more conditions of De-P-Carriers (carriers made by SAP 60min or ACP 60min)
- Change the order of size-selection. The size-selection will be performed prior PCR amplification.
Procedures
- Prepare the following samples
- E.coli internal marker (IM) (200bp): 43.6ng/uL
- 1/10 dilutted E.coli internal marker (IM) (200bp): 4.36ng/uL
- DNAse digested-cleaned (D-C) tRNA 109 ng/uL
Sample name B1 B2 B3 B4 B5 B6 B7 B8 200ng IM 50ng IM 10ng IM 50ng IM 10ng IM 0ng IM 0ng IM 0ng IM 300ng tRNA 450ng tRNA 490ng tRNA 450ng tRNA 490ng tRNA 500ng tRNA 500ng tRNA 500ng tRNA --------------------------------------------------------------------------------------------------------------------------------------------- E.coli IM (43.6ng/uL) 4.59 1.15 - 1.15 - - - - 1/10 E.coli IM (4.36ng/uL0 - - 2.29 - 2.29 - - - D-C-tRNA (78ng/uL) 3.85 5.77 6.28 5.77 6.28 6.41 6.41 6.41 H2O 91.56 93.08 91.43 93.08 91.43 93.59 93.59 93.59 --------------------------------------------------------------------------------------------------------------------------------------------- 100.00 100.00 100.00 100.00 100.00 100.00 100.00 100.00 uL NOTE: reactions B1, B2 and B3 will be added with De-P-carrier. Reactions B4 - B8 won't.
- Purify the DAN mixture with EtOH precipitation
- mimic the real procedures to remove the enzyme and buffers from WGA reactions
- Each sample (PCR product) has 100uL volume. Air dry the pellet. Dissolve the pellet in 34uL H2O.
End-repairing & Phosphorylation
- End-it Kit (EPICENTRE)
1rxn 8.5rxn DNA+H2O 34.0 - 10X buf. 5.0 42.5 2.5mM dNTP 5.0 42.5 10mM ATP 5.0 42.5 Enzyme 1.0 8.5 ------------------------------------ 50.0 136.0 136/8.5=16
- Mix the reaction by vortexing 5sec. Incubate at RT for 45min.
- Adding De-P-Carrier into the DNA mixture during QIAquick washing.
- Concentration of De-P-Carrier 1ug/30uL = 33.3ng/uL
- S30: 450ng for B4 reaction: 450/33.3=13.5uL
- S30: 490ng for B5 reaction: 490/33.3=14.7uL
- S30 :500ng for B6 reaction: 500/33.3=15.0uL
- S60 :500ng for B7 reaction: 500/33.3=15.0uL
- A60 :500ng for B8 reaction: 500/33.3=15.0uL
- Elute DNA in 28uL EB
A-tailing
- Exo-minus klenow DNA pol. kit (Epicentre)
1rxn 8.5rxn DNA+H2O 28.0 - 10X buf. 4.0 34.0 1mM dATP 6.0 51.0 Enzyme 2.0 17.0 ------------------------------------ 40.0 102.0 102/8.5=12
- Mix the reaction by vortexing 5sec. Incubate at 37C for 30min.
- QIAquick purification. Eluted in 20uL EB.
ligation
- T4 ligation kit (Enzymatic)
1rxn 8.5rxn DNA+H2O 11.0 - 2X rapid buf. 15.0 127.5 20uM Y-adaptor 2.0 17.0 T4 ligase 2.0 17.0 ------------------------------------ 30.0 161.5/8.5=19
- Mix the reaction by vortexing 5sec. Incubate at RT for 15min.
- QIAquick purification. Eluted in 20uL EB.
Size selection
- Only size select the first six reactions (reaction B7 and B8 are two extra negative controls).
- 20uL PCR product samples were run on 5-well PAGE (200V, 30min).
- Sample well: 20uL sample + 10uL 6X loading dye + 10uL 0.5X TBE buffer
- Ladder well: 0.5uL low mass ladder + 10uL 6X loading dye + 30uL 0.5X TBE buffer
File:Sam022810- B1 to B4 pre-cut.jpg File:Sam022810- B1 to B4 post-cut.jpg File:Sam022810- B5 to B8 pre-cut.jpg File:Sam022810- B5 to B8 post-cut.jpg
- DNA was recovered from the gel slice
- During the 37C incubation step (1X TE and homogenized gel slides), additional tRNA carriers were added into each reaction to protect sample DNA.
Sample name B1 B2 B3 B4 B5 B6 B7 B8 200ng IM 50ng IM 10ng IM 50ng IM 10ng IM 0ng IM 0ng IM 0ng IM 300ng tRNA 450ng tRNA 490ng tRNA 450ng tRNA 490ng tRNA 500ng tRNA 500ng tRNA 500ng tRNA --------------------------------------------------------------------------------------------------------------------------------------------- D-C-tRNA(78ng/uL) 3.85 5.77 6.28 5.77 6.28 6.41 6.41 6.41 uL
- Purify the DAN with Nanosap filter and EtOH precipitation.
- Air dry the DNA pellet in PCR hood (~5min). Elute the DNA in 20uL H2O.
Libraray amplification by qPCR
- 2X Fusion mastermix (Enzymatic)
1rxn 6.5rxn H2O 10.8 70.2 DNA 10.0 - PCR_f (10uM) 2.0 13.0 PCR_r (10uM) 2.0 13.0 SYBR 50X 0.2 1.3 2X Fusion enzyme 25.0 162.5 ------------------------------------ 50.0 195.0/6.5=30
- The amplification was stopped at the 8th cycle and 12th cycle.
TBE-PAGE validation
- 3uL PCR products were run on 10-well PAGE (200V, 30min).
- Sample well: 3uL sample + 3uL 6X loading dye + 3uL 0.5X TBE buffer
- Ladder well: 0.5uL low mass ladder + 3uL 6X loading dye + 6uL 0.5X TBE buffer
File:Sam030210-PCR amplified lib - 8th cycle.JPG File:Sam030210-PCR amplified lib - 12th cycle.JPG
- The library from B5 didn't showed up in 8th cycle due to the insufficinet amplification.
B1 B2 B3 B4 B5 B6 Input DNA 200ng 50ng 10ng 50ng 10ng 0ng tRNA 300ng 450ng 490ng 450ng 490ng 500ng De-P-Carrier 450ng 490ng 500ng Expected size: Nucleotides Prior-ligation Post-ligation -------------------------------------------------- tRNA N/A N/A Sample (E.coli) 200bp ~300bp Carrier (Lambda) 100bp ~200bp
Discussion
- Regardless which enzyme or condition was used, all dephosphorylated carriers are still ligated with adaptor in this test.
- Even I add the inactivation step (70C 10min)following End-repairing step, the situation was not imporved.
- B4-B6: De-P-Carrier prepared by SAP, 30min.
- B5: De-P-Carrier prepared by SAP, 60min.
- B6: De-P-Carrier prepared by ACP, 60min.
- Possible reasons of the appearance of adaptor-ligated carrier:
- The Dephosphorylation is not complete.
- The De-P-Carriere was rephosphorylated after End-repairing.
- The Phosphorylation "on templates (insert)" is not playing the critical roll for ligation.
- The method in this test (size selection prior PCR amplification) is still able to construct the library with only 10ng DNA (for both with or without carrier conditions).
- The early size selection method can generate the libraries with much lower unspecific amplification.
treated Regardless which enzyme or conditino were uuAll of Sol1: Adjust the dephosphorylation conditions.
- Sol2: Add heat inactivation stet right after End-reparing reaction.
- The smear (unspecific amplification) is weaker in those samples with lambda DNA carriers. Perhaps the Y-adaptor were comsumed more in those samples.
- I assumed that the overdose of Y-adaptor might be associated with the unspecific amplification.
- In the no lambda carries samples, even the 10ng input-DNA could be successfully made to library using the current protocl.