Jul 12, 2018
- Tibor Török1,2,3,4
- 1Department of Genetics;
- 2University of Szeged;
- 3Szeged, H-6726;
- 4Hungary
External link: https://doi.org/10.1371/journal.pone.0205920
Protocol Citation: Tibor Török 2018. Ancient DNA protocols. protocols.io https://dx.doi.org/10.17504/protocols.io.rmvd466
Manuscript citation:
Neparáczki E, Maróti Z, Kalmár T, Kocsy K, Maár K, Bihari P, Nagy I, Fóthi E, Pap I, Kustár
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: July 12, 2018
Last Modified: July 12, 2018
Protocol Integer ID: 13717
Keywords: ancient dna extraction from bone, performance of three ancient dna extraction method, ancient dna extraction, three ancient dna extraction method, dna contamination in human ancient dna research, human ancient dna research, ancient dna protocols ancient dna work, ancient dna, ancient dna from european early neolithic farmer, specialized ancient dna, dna solubilisation, dna extraction, ancient dna damage parameter, ancient bone, mg bone powder from tooth root, ancient dna damage pattern, controlling dna contamination, access to endogenous dna, mitochondrial dna capture, endogenous dna content, dna, library dna, biotinilated mtdna bait, human mitochondrial dna, endogenous dna, proportion of endogenous dna, multiplexed dna sequence capture, agilent 2200 tapestation genomic dna screentape, nucleic acids research, mg bone powder, mtdna, tapestation genomic dna screentape, multiplexed dna sequence capture of mitochondrial genome, generation dna sequencing data, mtdna bait, nucleotide, μl t4 dna polymerase, dna seq
Abstract
Ancient DNA work was performed in the specialized ancient DNA (aDNA) facilities of the Department of Genetics, University of Szeged, Hungary with strict clean-room conditions. In order to authenticate the results, we considered the latest recommendations of (Llamas et al. 2017) throughout of the experiments.
DNA extraction:
Note: This protocol is based on (Rohland and Hofreiter 2007), supplemented with partial predigestion (Damgaard et al. 2015) and using a GuHCl Binding Buffer modified after (Gamba et al. 2016).
- 100 mg bone powder from tooth root, petrous bone or other dense bone was predigested in 1 ml 0,5 M EDTA 100 µg/ml Proteinase K for 30 minutes at 48 oC, to increase the proportion of endogenous DNA (Damgaard et al. 2015),
- Then DNA solubilisation was done overnight at 48 oC in 1 ml extraction buffer containing 0.45 M EDTA, 250 µg/ml Proteinase K, 1% Triton X-100, and 50 mM DTT.
- DNA was bound to silica (Rohland and Hofreiter 2007) adding 6 ml Binding Buffer (5,83 M GuHCl, 105 mM NaOAc, 46,8% isopropanol, 0,06% Tween-20) and 150 µl silica suspension to the 1 ml extract, and the pH was adjusted between 4-6 with HCl.
- After 3 hours binding at room temperature silica was pelleted, and washed twice with 80% ethanol, then DNA was eluted in 100 µl TE buffer.
NGS library construction
Note: We used the double stranded library protocol of (Meyer and Kircher 2010) with double indexing (Kircher, Sawyer, and Meyer 2012), except that all purifications were done with MinElute columns . We also applied partial UDG treatment of (Rohland et al. 2015), but decreased the recommended USER and UGI concentrations to half (0.03 U/μL) and at the same time increased the incubation time from 30 to 40 minutes. This modification removed uracils with comparable efficiency to the original method.
DNA free negative control libraries were also made to detect possible contamination during handling or present in materials.
Partial UDG treatment:
| reagent | volume (μL) per sample | |
| Buffer Tango (10X) | 6 | |
| dNTPs (25 mM each) | 0,24 | |
| ATP (100 mM) | 0,6 | |
| USER (1 U/μL NEB) | 1,8 | |
| DNA extract | 51,36 | |
| Total: | 60 μL |
The reaction was incubated at 37oC for 40 minutes in PCR machine, with 40 oC lid temerature.
Then 1,8 μL UGI (Uracil Glycosylase Inhibitor, 2U/μL NEB) was added to the reaction, which was further incubated at 37oC for 40 minutes.
Blunt-End Repair:
- To each reaction we added 3 μL T4 polynucleotide kinase (10 U/μL) and 1,2 μL T4 DNA polymerase-t (5 U/μL), then incubated in PCR machine at 25°C for 15 minutes, followed by incubation at 12°C for 5 minutes and cooling to 4°C.
- 350 ul MinElute PB buffer (QIAGEN) was added to the reaction, then it was purified on MinElute columns. DNA was eluted in 20 ul EB prewarmed to 55 oC.
Adapter ligation:
| reagent | volume (μL) per sample | |
| T4 DNA ligase buffer (10X) | 4 | |
| PEG-4000 (50%) | 4 | |
| adapter mix (50 μM each) | 0,5 | |
| T4 DNA ligase (5 U /μL) | 1 | |
| H2O | 10,5 | |
| DNA | 20 ul | |
| Total: | 40ul |
- We incubated the reaction at 22°C for 30 minutes in PCR machine.
- Then 200 μL PB Buffer was added followed by MinElute purification. DNA was eluted in 20 ul EB.
Adapter Fill-In:
Note: We assembled the reaction below without library DNA, and the elution step from above was centrifuged directly on the fill-in reaction mix.
| reagent | volume (μL) per sample | |
| H2O | 14.1 | |
| ThermoPol reaction buffer (10X) | 4 | |
| dNTPs (25 mM each) | 0.4 | |
| Bst polymerase, large fragment (8 U/μL) | 1.5 | |
| Library DNA (from adapter ligation) | 20 | |
| Total: | 40ul |
- The reaction was incubated at 37°C for 20 minutes, then 200 ul PB was added followed by MinElute purification. Library was eluted in 20 ul EB.
Library preamplification:
Libraries were preamplified in 2 x 50 µl reactions containing 800 nM each of IS7 and IS8 primers, 200 µM dNTP mix, 2 mM MgCl2, 0,02 U/µl GoTaq G2 Hot Start Polymerase (Promega) and 1X GoTaq buffer, followed by MinElute purification. PCR conditions were 96 oC 6 min, 11 cycles of 94 oC 30 sec, 58 oC 30 sec, 72 oC 30 sec, followed by a final extension of 64 oC 10 min. Libraries were eluted from the column in 50 µl 55 oC EB buffer (Qiagen), and concentration was measured with Qubit (Termo Fisher Scientific). Libraries below 5 ng/µl concentration were reamplified in the same reaction for additional 5-12 cycles, depending on concentration, in order to obtain 50 µl preamplified library with a concentration between 10-50 ng/µl.
Double indexing:
50 ng preamplified libraries were double indexed according to (Kircher, Sawyer, and Meyer 2012) in a 50 µl PCR reaction containing 1 x KAPA HiFi HotStart ReadyMix (Kapa Biosystems) and 1000 nM each of P5 and P7 indexing primers. PCR conditions were 98 oC 3 min, 6 cycles of 98 oC 20 sec, 66 oC 10 sec, 72 oC 15 sec followed by a final extension of 72 oC 30sec. Indexed libraries were MinElute purified and their concentration was measured with Qubit, and size distribution was checked on Agilent 2200 TapeStation Genomic DNA ScreenTape.
Note: Lately we use 30 ng preamplified libraries and just 5 PCR cycles to avoid overamplification.
Mitochondrial DNA capture and sequencing:
Biotinilated mtDNA baits were prepared from three overlapping long-range PCR products as described in (Maricic, Whitten, and Pääbo 2010), but using the following primer pairs, L14759-H06378, L10870-H14799, L06363-H10888, described in (Haak et al. 2010).
Capture was done according to (Maricic, Whitten, and Pääbo 2010) with the following modifications: Just four blocking oligos, given below were used in 3 µM (each) final concentration:
BO1.P5.part1F: AATGATACGGCGACCACCGAGATCTACAC-Phosphate,
BO2.P5.part2F ACACTCTTTCCCTACACGACGCTCTTCCGATCT-Phosphate,
BO4.P7.part1 R GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT-Phosphate,
BO6.P7.part2 R CAAGCAGAAGACGGCATACGAGAT-Phosphate.
- For one capture 300 ng biotinilated bait was used with 30 µl Dynabeads MyOne Streptavidin C1 magnetic beads (Thermo Fisher Scientific).
- Double indexed libraries of 20 samples (300 ng each) were mixed and concentrated on MinElute columns, then captured together in a 64 µl hybridization reaction. When fewer samples were enriched, we used proportionally smaller amounts of baits.
- After washing, bead-bound enriched libraries were resuspended in 20 µl water and released from the beads in a 60 µl PCR reaction containing 1 X KAPA HiFi HotStart ReadyMix and 2000 nM each of IS5- IS6 library primers. PCR conditions were: 98 oC 1 min, 10 cycles of 98 oC 20 sec, 60 oC 30 sec, 72 oC 30 sec, followed by a final extension of 72 oC 30 sec. The captured and amplified library mix was purified on MinElute column and eluted in 15 µl EB.
- Before sequencing, libraries were quantified with Qubit, and quality checked and Agilent 2200 TapeStation Genomic DNA ScreenTape. Sequencing was done at the SeqOmics Biotechnology Ltd., using MiSeq sequencer with MiSeq Reagent Kit v3 (Illumina, MS-102-3003) generating 2x150bp paired-end sequences.
Note: Lately we perform low coverage shotgun sequencing prior to enrichment to estimate endogenous DNA content. Then 5-7 libraries with similar endogenous content are enriched together.
Data analysis
The adapters of paired-end reads were trimmed with the cutadapt software (Martin 2011) in paired end mode. Read quality was assessed with FastQC (S. Andrews 2016). Sequences shorter than 25 nucleotide were removed from this dataset. The resulting analysis-ready reads were mapped to the GRCh37.75 human genome reference sequence using the Burrows Wheeler Aligner (BWA) v0.7.9 software (Li and Durbin 2009) with the BWA mem algorithm in paired mode and default parameters. Aligning to the GRCh37.75 human reference genome that also contains the mtDNA revised Cambridge Reference Sequence (rCRS, NC_012920.1) (R. M. Andrews et al. 1999) helped to avoid the forced false alignment of homologous nuclear mitochondrial sequences (NumtS) to rCRS, though the proportion of NumtS, derived from low copy nuclear genome, is expexted to be orders of magnitudes lower than mtDNA in aDNA libraries. Samtools v1.1 (Li et al. 2009) was used for sorting and indexing BAM files. PCR duplicates were removed with Picard Tools v 1.113 (Broad Institute 2016). Ancient DNA damage patterns were assessed using MapDamage 2.0 (Jónsson et al. 2013), and read quality scores were modified with the rescale option to account for post-mortem damage. Freebayes v1.02 (Garrison and Marth 2012) was used to identify variants and generate variant call format (VCF) files with the parameters -q 10 (exclude nucleotids with <10 phred quality) and -P 0.5 (exclude very low probability variants). Each variant call was also inspected manually. From VCF files FASTA format was generated with the Genom Analysis Tool Kit (GATK v3.5) FastaAlternateReferenceMaker walker (McKenna et al. 2010).
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