用于化学转录障碍的内部修饰 DNA 模板的制备和特征分析

Eric  J. Strobel

doi:10.21769/BioProtoc.4141

Improve Research Reproducibility A Bio-protocol resource

提交稿件
订阅
CN
- EN - English
- CN - 中文

Peer-reviewed

Preparation and Characterization of Internally Modified DNA Templates for Chemical Transcription Roadblocking

用于化学转录障碍的内部修饰 DNA 模板的制备和特征分析

ES Eric J. Strobel email

发布: 2021年09月05日第11卷第17期 DOI: 10.21769/BioProtoc.4141 浏览次数: 2479

评审: Andrew SavinovTatiana MishaninaLionel Schiavolin

下载 PDF

Q&A

引用

Cited by

参见作者原研究论文

The authors used this protocol in:

Cover of The Journal of Biological Chemistry, featuring study using the protocol.

May 2020

实验方案合集

Cell Imaging - A Special Collection for Cell Bio 2023

相关实验方案

利用叉式PCR进行基因组步移以扩增未知侧翼DNA的实验方案

Hongjing Wu [...] Haixing Li

2025年01月20日 1658 阅读

基于部分重叠引物的PCR基因组步移技术用于未知侧翼DNA的鉴定

Mengya Jia [...] Haixing Li

2025年02月05日 656 阅读

使用PER-PCR进行基因步移挖掘未知侧翼DNA的实验方案

Zhou Yu [...] Haixing Li

2025年02月20日 776 阅读

Abstract

Site-specific transcription arrest is the basis of emerging technologies that assess nascent RNA structure and function. Cotranscriptionally folded RNA can be displayed from an arrested RNA polymerase (RNAP) for biochemical manipulations by halting transcription elongation at a defined DNA template position. Most transcription “roadblocking” approaches halt transcription elongation using a protein blockade that is non-covalently attached to the template DNA. I previously developed a strategy for halting Escherichia coli RNAP at a chemical lesion, which expands the repertoire of transcription roadblocking technologies and enables sophisticated manipulations of the arrested elongation complexes. To facilitate this chemical transcription roadblocking approach, I developed a sequence-independent method for preparing internally modified dsDNA using PCR and translesion synthesis. Here, I present a detailed protocol for the preparation and characterization of internally modified dsDNA templates for chemical transcription roadblocking experiments.

Graphic abstract:

Precise transcription roadblocking using functionalized DNA lesions

Keywords: Transcription (转录)

RNA (核糖核酸)

DNA lesion (DNA病变)

PCR (聚合酶链反应)

Translesion synthesis (跨损伤合成)

Cotranscriptional RNA folding (RNA共转录折叠)

Background

RNA begins to fold as it emerges from an RNA polymerase (RNAP) during transcription (Pan and Sosnick, 2006). Our ability to investigate the biological roles of nascent RNA structure and function therefore depends on the development of tools that can assess RNA cotranscriptionally. One successful approach towards this goal has been to leverage the extraordinary stability of the ternary RNAP-DNA template-nascent RNA complex to measure and manipulate nascent RNA in the context of arrested transcription elongation complexes (TECs) (Buenrostro et al., 2014; Tome et al., 2014; Watters et al., 2016; Strobel et al., 2017; Widom et al., 2018).

Multi-subunit RNAPs are remarkably processive enzymes that are capable of transcribing multi-kilobase operons in bacteria and tens of kilobases to megabases in eukaryotic genes (Core et al., 2008; Belogurov and Artsimovitch, 2019). The molecular forces that enable processive transcription elongation (Korzheva et al., 2000; Vassylyev et al., 2007a and 2007b) also render TECs notoriously resistant to dissociation in general. For example, when RNAP encounters a roadblock, such as a DNA-bound protein or a chemical DNA lesion, the TEC typically remains intact until either the roadblock is removed or a termination factor evicts RNAP from the DNA (Selby and Sancar, 1993 and 1994). When constructed in vitro by halting RNAP at a transcription roadblock, arrested TECs persist for exceptionally long periods of time. RNAP arrest by transcription roadblocking has consequently become the method of choice for structural and functional studies that require the display of nascent RNA molecules.

The development of high-throughput methods that use arrested RNAPs to display RNA underscores the need for versatile transcription roadblocking tools. Several roadblocking strategies that halt transcription elongation by colliding RNAP with a DNA-bound protein blockade have been developed: Sequence-specific protein roadblocks, such as the catalytically inactive EcoRI_E111Q mutant (Pavco and Steege, 1990) and the E. coli DNA replication terminator Tus (Tome et al., 2014), are attached to a DNA template by their respective recognition sequences. Streptavidin can be stably attached to template DNA using precisely (Frieda and Block, 2012) or randomly positioned (Strobel et al., 2017) biotin modifications. dCas9 can be reversibly loaded onto arbitrary DNA sequences to halt RNAP sequentially at multiple DNA positions (Widom et al., 2019). In contrast to the abundance of approaches for protein-mediated transcription roadblocking, methods for halting RNAP at DNA lesions have been conspicuously lacking despite the long-established fact that DNA damage causes transcription arrest. I previously addressed this technological gap by developing a sequence-independent method for preparing internally modified linear dsDNA using translesion synthesis and characterizing the transcription roadblocking properties of several DNA modifications (Strobel et al., 2020).

My chemical transcription roadblocking method complements the properties of protein-mediated roadblocking strategies in several ways. First, like biotin-streptavidin roadblocking, chemical transcription roadblocking is sequence-independent and therefore compatible with the preparation of complex sequence libraries. Second, chemical stall sites are fully functional in a minimal in vitro transcription reaction and are therefore compatible with diverse experimental conditions. Third, functionalized chemical stall sites can enable TEC manipulations that are not otherwise possible. For example, I previously showed that TECs that are arrested at a desthiobiotin stall site can be enriched by exclusion from streptavidin-coated magnetic particles. The primary disadvantage of chemical transcription roadblocking is that E. coli RNAP can bypass some DNA lesions over time. Nonetheless, in many cases, lesion bypass is extremely slow and will therefore not be prohibitive for most experiments: in the transcription reactions described below, TECs remain at a desthiobiotin-TEG stall site with a half-life of ~600 min, whereas unimpeded bacterial transcription occurs at 50-100 nt/s. Furthermore, these arrested TECs can persist stably for hours following nucleotide depletion (Strobel et al., 2020).

Here, I provide a detailed protocol for the preparation and characterization of internally modified linear dsDNA templates for chemical transcription roadblocking. I first describe considerations that must be taken into account during oligonucleotide design and provide a set of validated sequences for PCR amplification. I then present a straightforward protocol for the preparation of internally modified DNA using PCR and translesion synthesis and describe how to assess DNA template quality using denaturing and native polyacrylamide gel electrophoresis. Lastly, I present a single-round in vitro transcription protocol that can be used to verify the transcription roadblocking activity of the DNA template. Together, these protocols will enable any researcher with basic molecular biology expertise to successfully design and prepare internally modified DNA templates for the display of nascent RNA from arrested TECs.

Materials and Reagents

Consumables
1. Low retention 10 μl pipette tips (e.g., Neptune Scientific, catalog number: 2342S3.S)
2. Low retention 200 μl pipette tips (e.g., Neptune Scientific, catalog number: 2102.S)
3. Low retention 1,000 μl pipette tips (e.g., Neptune Scientific, catalog number: 2372.S)
4. 200 μl, 0.4 mm flat gel loading pipette tips (e.g., Laboratory Product Sales, catalog number: L113761)
5. Nuclease-Free 1.7 ml Microcentrifuge Tubes (e.g., Thomas Scientific, catalog number: 1149K01)
6. Nuclease-Free 2.0 ml Microcentrifuge Tubes (e.g., VWR, catalog number: 20170-170)
7. 2.0 ml Screw-Cap Tubes, w/ O-ring (e.g., Laboratory Product Sales, catalog number: L233226)
8. 0.2 ml 8-Strip PCR tube w/ dome cap (e.g., Laboratory Product Sales, catalog number: L216380)
9. Qubit^TM Assay Tubes (Invitrogen^TM, catalog number: Q32856)
10. 15 ml Conical Tubes (e.g., Laboratory Product Sales, catalog number: TR2000)
11. 20 ml Conical Tubes (e.g., Laboratory Product Sales, catalog number: TR2003)
12. 5 ml serological pipette (e.g., Laboratory Product Sales, catalog number: L310500)
13. 10 ml serological pipette (e.g., Laboratory Product Sales, catalog number: L311000)
14. 25 ml serological pipette (e.g., Laboratory Product Sales, catalog number: L312510)
15. Weigh boats (any source)
16. 10 ml Syringe (e.g., BD, catalog number: 302995)
17. 60 ml Syringe (e.g., BD, catalog number: 309653)
18. 20G 1½” Needle (e.g., BD, catalog number: 305176)
19. 0.2 μm Polyethersulfone (PES) syringe filter, sterile (e.g., VWR catalog number: 28145-501)
20. 150 mm Culture Dish (e.g., Corning^® catalog number: 430599)
21. Small 1-Ply Light-Duty Tissue Wipers (e.g., VWR, catalog number: 82003-820)
22. Large 1-Ply Light-Duty Tissue Wipers (e.g., VWR, catalog number: 82003-822)
23. Plastic-backed bench paper (e.g., Fisher Scientific, catalog number: 14-127-47)
24. Nitrile Gloves
25. Vaseline^® Petroleum Jelly Original
26. Rain-X^® Original Glass Water Repellent
27. Large binder clips (e.g., Staples 2” Binder Clips, Staples, catalog number: 10669)
28. AEP 30510400 ZipSafe Sealwrap, 18” × 2000’ (Amazon)
29. Razor blades
30. Aluminum foil
31. Dish soap
32. Plastic brush for cleaning sequencing gel plates

Reagents
Note: Chemicals should be Molecular Biology/Biotechnology Grade.
1. Nuclease-Free Water (e.g., Invitrogen^TM, catalog number: 10977015), store at room temperature (RT)
2. Milli-Q Water, store at RT
3. Deionized Water, store at RT
4. Diethyl pyrocarbonate (DEPC), >97%, (Thermo Scientific^TM, AAJ14710AC), store at -20°C
  Note: Handle DEPC in a chemical fume hood.
5. Tris (1 M), pH 8.0, RNase-free (Invitrogen^TM, catalog number: AM9855G), store at RT
6. EDTA (0.5 M), pH 8.0, RNase-free (Invitrogen^TM, catalog number: AM9260G), store at RT
7. Potassium Chloride (KCl) (2 M), RNase-free (Invitrogen^TM, catalog number: AM9640G), store at RT
8. Magnesium Chloride (MgCl₂), 1 M, RNase-free (Invitrogen^TM, catalog number: AM9530G), store at RT
9. Sodium Acetate (NaOAc) (3 M), pH 5.5 RNase-free (Invitrogen^TM, catalog number: AM9740), store at RT
10. 1× Tris-EDTA (TE) Solution (10 mM Tris pH 7.5, 0.1 mM EDTA), (e.g., Integrated DNA Technologies, catalog number: 11-05-01-05), store at RT
11. Tris Base (e.g., VWR, catalog number: 97061-794), store at RT
12. EDTA, Disodium Salt, Dihydrate (e.g., Invitrogen^TM, catalog number: 15576028), store at RT
13. Hydrochloric Acid (HCl) (e.g., Sigma-Aldrich, catalog number: 320331), store at RT with other acids beneath a fume hood.
  Caution: Hydrochloric acid is highly corrosive and must be handled in a chemical fume hood.
14. Sodium hydroxide (NaOH) (e.g., Sigma-Aldrich, catalog number: S8045), store at RT with other bases
  Caution: Sodium hydroxide is highly corrosive.
15. Boric Acid (e.g., Fisher Scientific, catalog number: BP168-500), store at RT
16. Sodium dodecyl sulfate sodium salt (SDS) (e.g., Millipore, catalog number: 7910-500GM), store at RT
17. Dithiothreitol (DTT) (e.g., Gold Biotechnology, catalog number: DTT100), store desiccated at -20°C
18. 100% Ethanol (200 Proof) (e.g., Decon Labs, catalog number: 2716), store at RT
19. Isopropanol (e.g., Sigma-Aldrich, catalog number: I9516-4L), store at RT
20. Glycerol (e.g., Sigma-Aldrich, catalog number: G5516-4L), store at RT
21. Phenol:Chloroform + Tris Buffer (e.g., Thermo Scientific^TM, catalog number: 17909), store at 4°C
  Caution: Phenol:chloroform should be handled in a chemical fume hood.
22. OmniPur Formamide, Deionized (e.g., Millipore, catalog number: 4650-500ML), store at 4 °C
  Caution: Formamide should be handled in a chemical fume hood.
23. Dimethyl sulfoxide (DMSO) (e.g., Fisher Scientific, catalog number: D128-500), store at RT
  Caution: Dimethyl sulfoxide should be handled in a chemical fume hood.
24. Ammonium persulfate (APS) (e.g., Sigma-Aldrich, catalog number: A3678-100G), store at RT
25. TEMED (Tetramethylethylenediamine) (e.g., Bio-Rad, catalog number: 1610801), store at RT
26. Bromophenol blue (e.g., Bio-Rad, catalog number: 1610404), store at RT
27. Xylene cyanole FF (e.g., Bio-Rad, catalog number: 1610423), store at RT
28. Ethidium bromide, 10 mg/ml (e.g., Invitrogen^TM, catalog number: 15585011), store at RT
  Note: Handle ethidium bromide in accordance with institutional guidelines.
29. Quick-Load^® Purple 100 bp DNA Ladder (New England Biolabs, catalog number: N0551L), store at RT
30. Low Range ssRNA Ladder (New England BioLabs, catalog number: N0364S), store at RT
31. SYBR Gold Nucleic Acid Stain (Invitrogen^TM, catalog number: S11494), store at -20°C
32. Deoxynucleotide (dNTP) Solution Mix (New England Biolabs, catalog number: N0447L), store at -20°C
33. dNTP Set (100 mM) (Invitrogen^TM, catalog number: 10297018), store at -20°C
34. 2-Amino-dATP (TriLink Biotechnologies, catalog number: N-2003), store at -20°C
35. 5-Propynyl-dCTP (TriLink Biotechnologies, catalog number: N-2016), store at -20°C
36. High Purity rNTP Set, 100 mM Solutions (ATP, CTP, GTP, UTP) (Cytiva Life Sciences, catalog number: 27202501), store at -20°C
37. UltraPure^TM BSA (Invitrogen^TM, catalog number: AM2616), store at -20°C
38. Rifampicin (Gold Biotechnology, catalog number: R-120-10), store dessicated at -20°C
39. GlycoBlue^TM Coprecipitant (Invitrogen^TM, catalog number: AM9516), store at -20°C
40. Qubit^TM dsDNA HS Assay Kit (Invitrogen^TM, catalog number: Q32854), some components stored at 4°C
41. Qubit^TM dsDNA BR Assay Kit (Invitrogen^TM, catalog number: Q32853), some components stored at 4°C
42. SeaKem GTG^TM Agarose (Lonza, catalog number: 50074), store at RT
  Critical: Agarose must be preparatory grade.
43. UreaGel 19:1 Denaturing Gel System (National Diagnostics, catalog number: EC-833), store at RT
  Caution: Contains acrylamide. Acrylamide is a neurotoxin and should be handled cautiously.
44. ProtoGel (30%) (National Diagnostics, catalog number: EC-890), store at RT
  Caution: Contains acrylamide. Acrylamide is a neurotoxin and should be handled cautiously.
45. QIAquick PCR purification kit (Qiagen, catalog number: 28106), store at RT
46. QIAquick Gel Extraction Kit (Qiagen, catalog number: 28706), store at RT
47. Internally modified oligonucleotides (Integrated DNA Technologies, see Table 1)
48. UTP, [α-³²P]-3000 Ci/mmol 10 mCi/ml (PerkinElmer, catalog number: BLU007H), store at -20°C
  Note: [α-³²P]-UTP must be handled in accordance with institutional radiation safety protocols.

Enzymes
1. Q5^® High-Fidelity DNA Polymerase (New England Biolabs, catalog number: M0491L), store at -20°C
2. Vent^® (exo-) DNA Polymerase (New England Biolabs, catalog number: M0257L), store at -20°C
3. Sulfolobus DNA Polymerase IV (New England Biolabs, catalog number: M0327S), store at -20°C
4. Thermolabile exonuclease I (New England Biolabs, catalog number: M0568L), store at -20°C
5. E. coli RNA Polymerase Holoenzyme (New England Biolabs, catalog number: M0551S), store at -20°C
  Note: E. coli RNA polymerase core and ⁷⁰ can be purified by well-established protocols (Marr and Roberts, 1997; Svetlov and Artsimovitch, 2015) and used to reconstitute the holoenzyme.

Prepared Solutions (see Recipes section)
1. DEPC-Treated Milli-Q Water
2. 10 mM Tris-HCl, pH 8.0
3. 10 mM Thermostability-enhancing dNTP Solution
4. 1× Tris-Borate-EDTA Buffer
5. 70% Ethanol
6. 10% SDS
7. 6× DNA Loading Dye (+SDS, XC only)
8. 10% APS
9. 1× Formamide Loading Dye
10. 3× Tris-Borate-EDTA Buffer
11. 6× DNA Loading Dye (non-denaturing)
12. 1 M DTT
13. 100 mM DTT
14. 10× Transcription Buffer
15. 20× NTP Solution
16. 5 mg/ml BSA
17. 2 mg/ml Rifampicin
18. 1 M Tris-HCl, pH 8.0
19. 0.5 M EDTA, pH 8.5
20. Stop Solution

Equipment

Autoclave
Fume Hood
-20°C and -80°C freezers (any source)
Refrigerator (4°C) (any source)
2 μl, 20 μl, 200 μl, and 1,000 μl micropipettes (any source)
Pipette Controller (e.g., Drummond, catalog number: 4-000-101)
Plastic tube racks for 1.7 ml, 15 ml, and 50 ml tubes (any source)
Lab Timer (e.g., Traceable^®, catalog number: 5004CC)
Ice bucket (e.g., SCIENCEWARE^®, catalog number: M16807-4002)
Erlenmeyer flasks (500 ml, 4 L) (any source)
Beakers (1 L, 2 L) (any source)
Autoclavable media bottles (500 ml, 1 L, and 2 L) (any source)
Graduated cylinders (10 ml, 50 ml, 200 ml, 0.5 L, 1 L, and 2 L) (any source)
Plastic 250 ml beaker (any source)
4 L polypropylene bottle (any source)
20 L carboy (any source)
Microwave (any source)
Vortex (e.g., Scientific Industries, catalog number: SI-0236)
Thermal cycler (e.g., Bio-Rad S1000 w/ 96-Deep Well Reaction Module, catalog number: 1852197)
Critical: 100 μl PCRs require a deep well thermal cycler. If 100 μl exceeds the maximum sample volume of your thermal cycler, aliquot the reaction into additional PCR tubes.
Refrigerated microcentrifuge (e.g., Eppendorf 5424 R, catalog number: 5406000046)
Mini centrifuge (e.g., VWR, catalog number: 76269-064)
Digital Dry Bath (e.g., Thermo Scientific^TM, catalog number: 88870001)
Lab Armor^TM Beads (Gibco^TM, catalog number: A1254301)
Aluminum block for 1.7 ml tubes (e.g., Thermo Scientific^TM, catalog number: 88880130)
Aluminum heating/block, holds 96 × 0.2 ml tubes (Sigma-Aldrich, catalog number: Z740270-1EA)
Analog thermometer (e.g., VWR, catalog number: 89095-600)
Digital thermometer (e.g., VWR, catalog number: 89094-750)
Qubit^TM 4 Fluorometer (Invitrogen^TM, catalog number: Q33238)
Rocking platform (e.g., Corning, catalog number: 6703)
Rotator (e.g., ATR, Rotamix Rotator RKVSD and end-over end rod, catalog numbers: 10101 and 10110)
pH meter (e.g., Mettler Toledo, S220-Bio, catalog number: 30019031)
Critical: The pH meter electrode must be compatible with Tris solutions.
Balance (e.g., Ohaus, catalog number: 30253007RM)
Analytical balance (e.g., Mettler Toledo, catalog number: 30029076)
Flat Spatula (e.g., VWR, catalog number: 82027-532)
Weighing Spatulas (any source)
Stir Plate (e.g., Corning PC-610D, catalog number: 6795620D)
Magnetic stir bars (e.g., VWR, catalog number: 58948-025)
Horizontal Gel Apparatus (e.g., Horizon 11-14 Midi Gel System, Gel Company, HZ1114)
Note: Comb should hold at least 50 μl.
Mini-PROTEAN Tetra Cell, 2-gel, for 1.0 mm handcast gels (Bio-Rad, catalog number: 1658003FC)
Sequencing Gel Apparatus (e.g., BRL Model S2; Gel Company, catalog number: S2-3040)
Note: Spacers and comb should be 0.4 mm thickness.
Basic power supply (e.g., Bio-Rad, catalog number: 1645050)
High voltage power supply (e.g., Bio-Rad, catalog number: 1645056)
UV Transilluminator (e.g., UVP catalog number: UV95045901)
Caution: Never expose eyes or skin to UV radiation.
Dark Reader Blue light Transilluminator (Clare Chemical, catalog number: DR89X)
Cardboard exposure cassette (e.g., Sigma-Aldrich, catalog number: E-9135, discontinued)
Storage Phosphor Screen, 35 × 43 cm (Cytiva Life Sciences, catalog number: 28956476)
Storage Phosphor Screen Image Eraser (Cytiva Life Sciences, catalog number: 29187190)
Typhoon Biomolecular RGB Biomolecular Imager (Cytiva Life Sciences, catalog number: 29187194)
Acrylic shielding for high-energy beta radiation
Note: I have found the items below useful when performing experiments with ³²P.
1. Vertical Bench-Top Beta Shield, 3/8” Thick (e.g., RPI, catalog number: BR-201)
2. 24-place Beta Block (e.g., Laboratory Product Sales, catalog number: 172644)
3. Sample Beta Box w/ ice compartment (e.g., Fisher Scientific, catalog number: S29137)
4. Acrylic Waste Box (e.g., ThermoScientic^TM, catalog number: 67459024)
5. Large Vertical Acrylic Shield (Denville Scientific, catalog number S0260-S)
6. Medium Vertical Acrylic Shield (Denville Scientific, catalog number S0180-S)
7. Large Acrylic Storage Container (e.g., Mitchell Plastics, catalog number: RP-400)
8. Small Acrylic Storage Container (e.g., IBI Scientific, catalog number: RB-100)
9. Pipette tip disposal box (Thomas Scientific, catalog number: 1216J05)

Procedure

English

中文翻译

文章信息

版权信息

如何引用

Readers should cite both the Bio-protocol article and the original research article where this protocol was used:

Strobel, E. J. (2021). Preparation and Characterization of Internally Modified DNA Templates for Chemical Transcription Roadblocking. Bio-protocol 11(17): e4141. DOI: 10.21769/BioProtoc.4141.
Strobel, E. J., Lis, J. T. and Lucks, J. B. (2020). Chemical roadblocking of DNA transcription for nascent RNA display.J Biol Chem 295(19): 6401-6412.