- Open Access
A cost-effective method for Illumina small RNA-Seq library preparation using T4 RNA ligase 1 adenylated adapters
© Chen et al.; licensee BioMed Central Ltd. 2012
- Received: 2 July 2012
- Accepted: 22 August 2012
- Published: 20 September 2012
Deep sequencing is a powerful tool for novel small RNA discovery. Illumina small RNA sequencing library preparation requires a pre-adenylated 3’ end adapter containing a 5’,5’-adenyl pyrophosphoryl moiety. In the absence of ATP, this adapter can be ligated to the 3’ hydroxyl group of small RNA, while RNA self-ligation and concatenation are repressed. Pre-adenylated adapters are one of the most essential and costly components required for library preparation, and few are commercially available.
We demonstrate that DNA oligo with 5’ phosphate and 3’ amine groups can be enzymatically adenylated by T4 RNA ligase 1 to generate customized pre-adenylated adapters. We have constructed and sequenced a small RNA library for tomato (Solanum lycopersicum) using the T4 RNA ligase 1 adenylated adapter.
We provide an efficient and low-cost method for small RNA sequencing library preparation, which takes two days to complete and costs around $20 per library. This protocol has been tested in several plant species for small RNA sequencing including sweet potato, pepper, watermelon, and cowpea, and could be readily applied to any RNA samples.
- Small RNA sequencing
- Directional mRNA sequencing
- 3’ RNA adapter
- T4 RNA ligase 1
The rapidly increasing NextGen sequencing capacity is enabling researchers to combine more samples for multiplexed sequencing, and the sequencing cost itself could be less than that of the library preparation . We have previously reported a high-throughput RNA sequencing strategy that has significantly lowered the library preparation cost . Here we sought to develop an alternative protocol that would also simplify the small RNA library preparation. We note that both the Illumina small RNA sequencing and directional mRNA sequencing library construction protocols are based on the early microRNA cloning strategies , in which two adapters are sequentially attached to the RNA molecule to create the priming sites for subsequent PCR amplification. The 5’ adapter is a conventional RNA oligo that can be synthesized by commercial oligo manufacturers. The 3’ adapter is a modified DNA oligo containing a 5’5’-adenyl pyrophosphoryl moiety and a 3’ blocking group such as amine or dideoxylnucleotides. The adenyl modification on 3’ adapter is crucial for the library preparation as it enables the adapter to be ligated to RNA in the absence of ATP by a truncated form of T4 RNA ligase 2. This effectively prevents small RNA self-ligation and concatenation. Despite the simplicity of this method, the adenylated DNA oligos are very costly to synthesize, and few are available commercially.
It has been reported that T4 DNA ligase can convert DNA oligos to pre-adenylated adapters . In a ligation reaction, T4 DNA ligase first adenylates the donor DNA that has a 5’ phosphate, and the adenylated intermediate reacts with the acceptor DNA with a free 3’ hydroxyl group, resulting in phosphodiester bond formation. This process could be interrupted, allowing the adenylated intermediate to be purified. However, the adenylation efficiency of T4 DNA ligase is inconsistent and several improvements have been suggested to optimize the reaction . We reason that the difficulties of utilizing T4 DNA ligase to generate adenylated adapters are partly due to the fact that it works best on double-stranded substrate, while the desired adapter is a single-stranded molecule. Hence, an RNA ligase could be a more suitable enzyme for adapter adenylation, since RNA ligation also generates a 5’ adenylated donor intermediate .
In this report, we demonstrate that T4 RNA ligase 1 can efficiently adenylate DNA oligos with 5’ phosphate and 3’ blocking group, and we have optimized the reaction condition for large-scale adapter production. Using the enzymatically adenylated adapters, we developed a rapid and cost-effective protocol to generate small RNA sequencing libraries.
Agarose gel electrophoresis system
Polyacrylamide gel electrophoresis system
Qubit Fluorometer (Invitrogen)
T4 RNA liagse 2, truncated (NEB)
50% PEG8000 (NEB)
10 mM ATP (NEB)
RNase Inhibitor (Promega)
T4 RNA ligase 1 (Enzymatics)
SuperScriptIII Reverse Transcriptase (Invitrogen)
Phusion Hotstart DNA Polymerase (NEB)
MinElute Gel Extraction kit (Qiagen)
Quant-iT HS DNA assay kit (Inivtrogen)
5’ adapter RNA oligo
5’ adapter: GUUCAGAGUUCUACAGUCCGACGAUC
3’ adapter oligos used for adenylation
3’ non-multiplex adapter (BL1): Phosphate-CTGTAGGCACCATCAAT-amine.
3’ multiplex adapter: Phosphate-CAGATCGGAAGAGCACACGT-amine.
Substrate dA: Phosphate-ACTTCGTATGCCGTCTTCTGCTT-amine
Substrate dT: Phosphate-TAGTCGTATGCCGTCTTCTGCTT-amine.
Substrate dC: Phosphate-CTGTCGTATGCCGTCTTCTGCTT-amine.
Reverse transcription primers
Non-multiplex RT primer: amine-ATTGATGGTGCCTACAG.
Multiplex RT primer: amine-ACGTGTGCTCTTCCGATCTG.
Library PCR amplification primers
Universal forward PCR primer (* indicates phosphothio modification): AATGATACGGCGACCACCGAGATCTACACGACAG GTTCAGAGTTCTACAGTCCGACGAT*C.
Non-multiplex reverse PCR primer: CAAGCAGAAGACGGCATACGAGATTGATGGTGCCTACA*G.
Multiplex reverse PCR primers with 6 nt barcode (NNNNNN indicates the location of TruSeq index sequences):
Dissolve the 5’ phosphorylated and 3’ blocked DNA oligo in RNase-free water to a final concentration of 100 uM.
Setup a reaction in 0.2 ml PCR tube containing 10 uL oligo, 10 uL 10x T4 RNA ligase 1 buffer, 40 uL 50% PEG8000, 35 uL RNase-free water and 5 uL T4 RNA ligase 1, and incubate overnight at room temperature.
Optional: setup multiple reactions if more adenylated adapters are required.
Purify the adenylated adapter using a Sephadex G-25 or silica-based spin column, e.g., Qiagen Nucleotide Removal Kit. Adjust the adapter concentration to 10 uM with RNase-free water. Note: In this reaction, T4 RNA ligase 1 will first adenylate the 5’ phosphorylated DNA oligo and attempt to join it with a suitable acceptor molecule with a 3’ hydroxyl group. The 3’ end of the oligo is block with amine and could not take part in the ligation reaction, leading to accumulation of the adenylated intermediate.
3’ adapter ligation
Denature the sRNA sample at 65°C for 30 sec, immediately chill on ice.
Denature the adenylated 3’ adapter at 65°C for 30 sec, immediately chill on ice.
Setup the ligation reaction with 8 uL small RNA, 1 uL adapter (10 uM), 2 uL 10x T4 RNA ligase buffer without ATP, 0.5 uL RNase inhibitor, 5 uL PEG8000 and 0.5 uL T4 RNA ligase 2, truncated. The reaction is incubated at 25°C for 4 h or 18°C overnight. Note: ligation reaction must be performed in the absence of ATP to prevent self-ligation of the small RNA that has a 5’ phosphate. Successfully ligated small RNA could be visualized on Urea-PAGE (Figure 1A).
Add 0.5 uL reverse transcription primer (20 uM) to the ligation reaction, heat inactivate the reaction at 65°C for 15 min and incubate the reaction at 25°C for 10 min.
Optional: to minimize adapter dimer formation in the subsequent PCR enrichment, the ligated sRNA could be PAGE purify before proceeding to the following 5’ adapter ligation steps.
5’ adapter ligation
Denature the 5’ adapter (10 uM, dissolved in RNase-free water) at 65°C for 30 sec, immediately chill on ice.
Setup the 5’ ligation reaction with 20.5 uL 3’ ligation product, 1 uL 5’ adapter (10 uM), 1 uL 10x T4 RNA ligase 1 buffer with ATP, 0.5 uL RNase Inhibitor, 2 uL 10 mM ATP, 4 uL RNase-free water and 1 uL T4 RNA ligase 1. The reaction is incubated at 25°C for 4 h or 18°C overnight. Note: the 3’ end of the small RNA has already been ligated to the 3’ adapter that has an amine group at the 3’ end, and could no longer take part in the ligation reaction; thus its 5’ end could be ligated to an RNA oligo in the presence of ATP.
Add 2 uL dNTP (10 mM each), 3 uL DTT (100 mM), 9 uL 5xSuperScriptIII Frist Strand reaction buffer, and 1 uL SuperScriptIII reverse transcriptase to the 5’ ligation reaction.
Incubate the reaction at 50°C for 1 h, and heat inactivate the reverse transcriptase at 75°C for 15 min.
Assemble the PCR reaction with 10 uL RT product, 1 uL forward primer, 1 uL reverse primer, 1 uL dNTP, 6 uL 5x Phusion HF buffer, 10.5 uL water and 0.5 uL Phusion DNA polymerase. The remaining RT product could be stored at −20°C.
Perform 12 to 15 cycles of PCR amplification as followed: 94°C 2 min, 12–15 cycles of 98°C for 12 sec, 65°C for 30 sec and 72°C for 30 sec, and a final extension at 72°C for 2 min.
Seperate the PCR product on a 2% agarose gel. Note: The multiplex sRNA-Seq library and adapter dimer are 150 and 120 bp respectively (Figure 1B); whereas the reverse transcription and PCR primers used in the Illumina non-multiplex library preparation lack the barcode sequences, hence the sizes of non-multiplex sRNA-Seq library and adapter dimer are smaller at 120 and 90 bp, respectively.
Cut the band corresponding to the small RNA library and gel-purify the product with Qiagen MinElute kit.
Optional step: adjust PCR cycles accordingly to avoid over or insufficient PCR amplification.
Quantify and pool libraries for sequencing
Quantify the purified library using QuaniT HS DNA assay kit.
Use 10 uL of library with a final concentration no less than 2 ng/ul for each lane of Illumina sequencing.
Optional: if multiplex sRNA-Seq libraries were used, mix equal amount (10 ng) of each libraries, concentrate using Qiagen MinElute kit, and use 10 uL library with a final concentration no less than 2 ng/ul for each lane of Illumina sequencing.
Funding is provided by National Science Foundation (IOS-1110080) to Z.F., Human Frontier Science Program (LT00076/2009) to S.Z, National Science Council of Taiwan Fellowship to Y.C. and the Chinese National Natural Science Foundation (NSFC-3090243) to B.L.
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