Optimized protocols for RNA-induced silencing complex assembly and cleavage in cultured Drosophila cells.

Here, we provide an optimized RNA-induced silencing complex (RISC) assembly and cleavage protocol in vitro without using radiolabeled RNA. The protocol is useful to characterize the biochemical properties of the RISC. We describe the preparation of RNA probes, the target RNA, and Drosophila cell lysates for RISC assembly assay. We then detail AGO1 complexes immunoprecipitation for RISC cleavage assay. This protocol can detect RISC assembly and cleavage products within 5 days. Moreover, it can detect 5'- and 3'-cleavage products simultaneously. For complete details on the use and execution of this protocol, please refer to Gao et al. (2022).

Before you begin

Small interfering RNAs (siRNAs) and microRNAs (miRNAs) mediated gene silencing are a major process of gene expression at the transcriptional and post-transcriptional levels (Iwakawa and Tomari, 2022; Treiber et al., 2019). Small RNAs bind to Argonaute (AGO) proteins to form RISC to silence their target mRNA by RNA cleavage or by preventing protein translation (Bartel, 2018; Duchaine and Fabian, 2019). AGOs, as the catalytic core of RISC, play essential roles in mediating sequence-specific target gene silencing.

To achieve their function for target gene silencing. siRNAs and miRNAs must form RISC with AGO proteins in a similar manner. RISC assembly is divided into two steps: the loading step and the maturation step. In the loading step, a small RNA duplex is loaded into the AGO protein to form the pre-RISC (Iwakawa and Tomari, 2022). In the maturation step, the duplex is separated, and only the guide strands reside in the AGO protein to form the mature RISC via wedging and passenger ejection (Kwak and Tomari, 2012). Mature siRNA-RISC induces the perfectly complementary target mRNA decay via cleavage activity, and mature miRNA-RISC generally causes the translational repression of partially complementary target mRNA.

Further applications into therapeutics of RISC arise from the fact that siRNAs and miRNAs can be designed to target mRNA for silencing, and many factors can fine-tune the core silence activity of RISC. In vitro RISC assembly and cleavage assay provides powerful biochemical readouts to assess the activity and stability of RISC. Agarose native gel electrophoresis has been used to detect in vitro AGO-RISC assembly (Kawamata et al., 2009) and cleavage (Meister et al., 2004; Miyoshi et al., 2005) to investigate the molecular mechanism of RISC biogenesis in Drosophila AGO1 or human AGO2 pathways. However, previous protocols depended on radiolabeled RNA (Kawamata and Tomari, 2011) and required labeling and gel assay steps to be performed in an isotope lab. Here, we describe a similar agarose native gel electrophoresis system to analyze mature AGO-RISC assembly and cleavage without using radiolabeled RNA probes.

Preparation of the ASO for AGO1-RISC assembly

Timing: Approximately 2 days

Anti-miR-9b antisense oligonucleotide (ASO) design and synthesis.

Design anti-miR-9b ASO with 5′-FAM and 3′-2-O-methylated modification, complementary to miR-9b, except for one mismatch in the central region (Figure 1).

Figure 1

Schematic of the Anti-miR-9b antisense oligonucleotide

This ASO is designed to have a central bulge to prevent endo-nucleolytic cleavage by AGO1-RISC.

Other fluorescence modifications such as Cy3 or Cy5 would also work.

CRITICAL: The RNA probe is very sensitive to the RNases. All the steps are conducted by using fresh RNase-Free water and RNase-Free pipet tips.

Preparation of the dsRNA

Timing: Approximately 1 day

dsRNA synthesis (Figure 2).

Figure 2

Schematic of dsRNA synthesis

Preparation of the in vitro transcriptional template by PCR. Prepare DNA templates of dsRNAs from Drosophila cDNA with gene specific primers harboring the T7 promoter sequence. Gene specific primers used to prepare the templates are listed in key resources table.

In vitro transcription reaction. Because the DNA templates used for synthesizing dsRNA contain the T7 promoter sequence at both 5′ and 3′ sides, the templates can be used to synthesize both sense and antisense RNA sequences by the T7 RiboMAX Express Large-Scale RNA Production Kit (Promega) according to the standard protocol.

Sense and antisense RNAs are annealed to generate dsRNAs. Briefly microfuge the tube and collect the RNA solution at the bottom of the tube. Use the PCR program as follows to perform the annealing.

dsRNA recovery and quantitation. Before the recovery procedure, perform DNase I treatment to remove the template DNA. Purify the dsRNAs following instructions of the T7 RiboMAX Express Large-Scale RNA Production Kit. These procedures remove the nucleotides, short oligonucleotides, proteins, and salts from dsRNAs. Quantitation can be determined by Nanodrop (Thermo Fisher Scientific).

Store the dsRNA at −20°C or −80°C for up to one year.

Preparation of the agarose gel

Timing: Approximately 4 h

Vertical agarose gel preparation.

Clean and dry the glass plates to avoid the formation of air bubbles while pouring the gel.

Assemble the glass plates and set them up in a standing (vertical) position with the gel casting equipment (Tanon).

For a 102 × 85 × 1.5 mm plate, use 10 mL of TBE-agarose. Add 0.3 g agarose to 20 mL 0.5 × TBE solution in a 150 mL conical flask.

Melt the agarose in a microwave oven until it is completely dissolved.

Carefully and slowly pour the agarose into the glass plates, and immediately insert a 1.5 mm, 15-well comb between the glass plates.

When the gel has solidified, carefully remove the comb. These gels should be stored at 4°C.

Preparation of substrate RNAs for the cleavage assay

Timing: Approximately 8 h

Substrate RNAs preparation (Figure 3). See troubleshooting 2 and 4.

Figure 3

Schematic of cleavage substrate 1 preparation

Preparation of the transcriptional template by PCR.

Synthesize the partially complementary oligonucleotides containing the miR-9b cleavage site as follows.

miR-9b-S:

5′-GAACAATTGCTTTTACAGATGCACATATCGAGGTGAACATCACGTACGCATACAGCTAAAATCACCAAAGATCGGTTGGCAGAAGCTAT-3′.

miR-9b-AS:

5′-GGCATAAAGAATTGAAGAGAGTTTTCACTGCATACGACGATTCTGTGATTTGTATTCAGCCCATATCGTTTCATAGCTTCTGCCAACCGA-3′.

Use the miR-9b-S and miR-9b-AS oligonucleotides for a PCR fill-in reaction via the PCR program.

PCR program: 60 s at 95°C, 5 min at 72°C, then cooling to 4°C.

For the second PCR amplification reaction, directly add 2 μL of T7 and SP6 primer (10 μM) to the PCR mixture. Set up the following PCR program.

Purify the PCR products after separation on a 1.5% agarose gel via gel DNA extraction according to the instructions.

Ligate the PCR fragment into the pEASY cloning vector using the pEASY-Blunt Zero Cloning Kit.

Perform sequencing using the M13 forward and reverse primers to verify positive colonies.

Set up another PCR mixture using the template from a sequence-verified positive colony and use the PCR program from step (iv) above. The PCR products from this step will be used as the template for in vitro transcription.

Capped transcription reaction for cleavage substrate 1 preparation.

Assemble the capped in vitro transcription mixture at room temperature (22°C–28°C) according to the instruction of the mMESSAGE mMACHINE kit as follows.

Mix thoroughly by gently pipetting the mixture up and down, and then briefly microfuge the tube and collect the solution at the bottom of the tube.

Incubate at 37°C for 4 h or overnight (4–12 h).

The mMESSAGE mMACHINE Kit is designed for optimal function with transcription templates in the 300–1,000 base range. In general, maximum yield can be achieved after a 2 h incubation. The second hour of incubation is necessary for transcription of < 300 base products.

Add 1 μL TURBO DNase, mix well and incubate at 37°C for 15 min.

Recover the RNA by lithium chloride precipitation according to the standard protocol. The RNA resulting from capped in vitro transcription provides the cleavage substrate 1 for the RISC cleavage assay.

Cleavage substrate 2 preparation.

Synthesize the 3′-RNA adaptor designed with both 5′-phosphate and 3′-6-FAM modification. 5′-phosphate-GrUrGrCrUrCrGrArGrUrCrGrCrGrGrCrCrGrCrArArGrGrArArCrArUrUrCrGrGrC-3′-6-FAM.

Ligate the 3′-RNA adaptor to cleavage substrate 1 by T4 RNA ligase 1 following the manufacturer’s instructions as follows (Figure 4).

Figure 4

Schematic of cleavage substrate 2 preparation

Incubate at 25°C for 4 h.

Purify the ligated RNA by size selection (> 200 nucleotides) using the Separated Fraction of the ZYMO-Spin Column, and use the purified ligated RNA for cleavage substrate 2 (Figure 5).

Figure 5

Purification and size selection of the cleavage substrate

CRITICAL: Avoid multiple freezes and thaw cycles for the RNA.

Preparation of buffers and solutions

Timing: Approximately 1 day

Preparation of lysis buffer for RISC assembly lysate preparation.

Refer to Materials and equipment.

Preparation of the 5 × TBE solution.

Refer to Materials and equipment.

Preparation of the RISC assembly reaction mixture.

Refer to Materials and equipment.

Preparation of immunoprecipitation (IP) lysis buffer.

Refer to Materials and equipment.

Preparation of IP washing buffer.

Refer to Materials and equipment.

Preparation of cleavage reaction buffer.

Refer to Materials and equipment.

Design qPCR primers for RNAi efficiency detection

Timing: Approximately 20 min

Primers used in the protocol are listed in the key resources table.

Key resources table

Materials and equipment

CRITICAL: DTT is a hazardous chemical. Carefully work under a chemical hood, and must wear gloves and a lab coat when handing. DTT waste needs to be collected and disposed of according to institute regulations.

Distilled H2O treated with 0.1% diethylpyrocarbonate (DEPC) can be used instead of commercial RNase Free H2O.

Step-by-step method details

Production of S2 lysates for RISC assembly

Timing: 4 days

This first part of the protocol is modified from a previous publication (Kawamata et al., 2009). This section describes how to prepare the cell lysates that will be used for RISC assembly assay.

Preparation of Drosophila S2 cells.

Culture Drosophila S2 cells in insect cell culture medium (Gibco) supplemented with penicillin-streptomycin and 10% FBS at 27°C.

To keep a healthy S2 cell culture going, the passage numbers of S2 cell is limited in 10–15.

Dilute confluent cells (∼1 × 107 cells/mL) and seed at a density of 5 × 105 cells/mL.

dsRNA treatment.

Seed S2 cells into a 10 cm dish with volumes of 10 mL at a density of 1 × 105 cells/mL and prepare for RNAi.

Thaw the frozen dsRNA reagents and place them on ice.

Add 8 μg dsRNA for targetting each gene(dcr-2, r2d2, ago2, or ago1 (3′-UTR)) to the cell culture medium and shake gently.

Transfer 1 mL of cells from the 10 cm dish to a 12-well plate to detect the efficiency of RNAi knockdown. See troubleshooting 1.

Plasmid transfection.

After 24 h of dsRNA treatment, prepare for plasmid transfection.

Preheat the Lipofectamine 2000 and Opti-MEM at room temperature (22°C–28°C).

Add 8 μg pAc5.1-Flag-AGO1 and 5 μg of pAc5.1-miR-9b plasmids to 500 μL Opti-MEM, and vortex the mixture.

The transfection of the miRNA is not essential. It depends on the expression levels of miRNA in the cell line.

Add 20 μL Lipofectamine 2000 to 500 μL Opti-MEM, and vortex the mixture.

Add diluted plasmids to the diluted Lipofectamine 2000 mixture.

Vortex the mixture, and incubate at room temperature (22°C–28°C) for 15 min.

Add the plasmid-lipid complex dropwise to the cell medium of the 10 cm dish and shake gently to mix.

qRT-PCR to confirm the efficiency of RNAi knockdown.

Design primers to perform the qPCR. Primers used for qPCR are listed in the key resources table.

After 72 h of dsRNA treatment, collect cells for subsequent real-time PCR.

Extract total RNA from the S2 cells treated with dsRNAs by the Trizol method.

Prepare cDNA with the HiScript III Reverse Kit (Vazyme) according to the instructions and dilute to a volume of 100 μL.

Set up the qRT-PCR reaction system.

Run the real-time PCR instrument.

Calculate the efficiency of RNAi knockdown. The relative mRNA expression is determined using the formula: 2-Ct method (Schmittgen and Livak, 2008) (Figure 6). See troubleshooting 1.

Figure 6

Relative expression levels of indicated genes in S2 cells treated with dsRNA measured by qRT-PCR

(A–D) S2 cells were treated with dsRNAs against dcr-2 (A), r2d2 (B), ago1 (C) or ago2 (D). Three days post dsRNA treatment, expressions of indicated genes were analyzed by qRT-PCR analysis. The two-tailed Student's t test was used to analyze statistical variance. Error bars indicate mean ± s.d (n=3). ∗∗∗, p<0.001, ∗∗∗∗, p<0.0001.

The TaqMan probes can be used instead of SYBR Green mixture and oligonucleotides.

Preparation of cell lysates.

After 48 h of transfection, collect the transfected S2 cells by centrifugation at 500 g for 5 min at 4°C, and then wash cells with cold PBS twice.

The waste of cell culture medium and the PBS needs to be collected and thoroughly mixed with an appropriate amount of 84 disinfectants, then disposed of according to institute regulations.

Resuspend cells in 1 mL lysis buffer (freshly supplemented with 2 mM DTT and protease inhibitor cocktail) and transfer to a pre-chilled Dounce homogenizer.

Dissolve one Complete EDTA-free protease inhibitor tablet in 500 μL lysis buffer as 100× stock solutions. Prepare freshly before use.

Prepare homogenates by performing 50 strokes using the tight pestle.

CRITICAL: This step should be performed on ice.

CRITICAL: Between samples, clean the Douncer and pestle with lysis buffer 3 times to avoid cross-contamination between different samples.

Clear the lysates by centrifugation at 15,000 g for 15 min at 4°C.

Transfer the supernatant and aliquot 50 μL/tube.

Freeze the lysates using liquid nitrogen and store them at −80°C.

We recommend immediately starting the AGO-RISC assembly reaction using fresh lysates.

Instead of the lysates prepared from S2 cells overexpressing AGO1, and in which dcr-2, r2d2, ago2, and ago1 are knocked down, the lysates prepared from the embryo of dcr-2 mutant flies can be used (Lee et al., 2004).

CRITICAL: Avoid multiple freezes and thaw cycles.

Pause point: The lysates can be stored at −80°C for up to one month.

Native gel analysis of AGO1-RISC assembly

Timing: 4 h

This section describes how to perform the in vitro RISC assembly.

Before beginning the in vitro RISC assembly, set up the agarose gel in the electrophoresis tank and fill it with pre-chilled 0.5 × TBE buffer.

Cooling the electrophoresis buffer is critical to detect complexes in the AGO1-RISC assembly. It is optimal to perform the electrophoresis at 4°C.

Prepare the in vitro RISC assembly as follows.

Incubate the mixture at 27°C for 40 min. See troubleshooting 3.

Load 3 μL of the assembly products into the 1.5% agarose native gel. See troubleshooting 5.

CRITICAL: Washing the gel and the gel wells with 0.5 × TBE buffer before running is essential for a good resolution.

Load 3 μL of 2 × RNA loading dye and perform electrophoresis at 300 V in cold 0.5 × TBE buffer for 20 min.

CRITICAL: We have noticed that the RISC assembly sample will not rapidly load to the bottom of the wells, likely due to the RISC assembly mixture not containing glycerol. We load the sample using long pipet pips to sink the sample to the bottom of the wells.

End the electrophoresis, and keep the gel attached to the glass plate.

Perform phosphor imaging to detect the mature AGO1-RISC.

Immunoprecipitation of AGO1 complexes for cleavage assay

Timing: 8–12 h

This section details the associated procedures of immunoprecipitation of AGO1 complexes. This part of the protocol is critical since the immunoprecipitation of AGO1 complexes will be used for the RISC cleavage assay.

Perform the cell culture as described under production of S2 lysates for RISC assembly.

Preparation of the cell lysates.

Harvest S2 cells by centrifugation at 500 g for 5 min.

Wash cells two times with cold PBS.

Add 1 mL of lysis buffer per 10 cm dish, resuspend the cell pellet by pipetting to ensure cells are fully lysed, and incubate on ice for 10 min.

Centrifuge at 12,000 g for 15 min at 4°C.

Carefully transfer the supernatant to new tubes and aliquot a 30 μL sample as the input fraction for western blot analysis.

When we transfer supernatant, do not disturb the pellets.

CRITICAL: Buffers should be pre-chilled on ice, and the centrifuge should be pre-cooled to 4°C.

Immunoprecipitation.

For immunoprecipitation of endogenous AGO1, incubate the supernatants with anti-AGO1 antibody or control IgG by rotation at 4°C for 5 h or overnight (6–12 h).

Use 20 μL of protein A/G agarose beads per sample.

Wash the beads once with 1 mL lysis buffer.

Add the washed beads to the lysates and incubate at 4°C for 3 h on a rotator.

Wash the samples three times with washing buffer.

Transfer the beads to a fresh tube and take an aliquot of 5 μL beads as the immunoprecipitation fraction for western blot analysis.

CRITICAL: All steps should be performed on ice or at 4°C.

RISC cleavage assay

Timing: 5 h

The section of this protocol is modified from a previous publication (Miyoshi et al., 2005), and this section describes how to perform the RISC cleavage assay in vitro.

Remove the supernatant.

Prepare the in vitro RISC cleavage reaction mixture as follows.

Incubate at 27°C for 2 h.

Add 1 mL of Trizol reagent to the cleavage RNA sample and pipet the sample up and down several times to homogenize.

Incubate for 10 min to allow complete dissociation of the AGO1-RNA complex.

Add 0.2 mL of chloroform to 1 mL of Trizol, cap the tube and mix thoroughly by shaking.

Incubate at room temperature (22°C–28°C) for 5 min.

CRITICAL: Trizol reagent and chloroform are hazardous solutions. Carefully work under a fume hood, must wear gloves and a lab coat. Trizol and chloroform waste must be collected and disposed of according to institute regulations.

Centrifuge the sample for 15 min at 13,000 g at 4°C.

Transfer 0.5 mL of the aqueous phase to a new tube.

After centrifugation, three phases will be obtained. An upper aqueous phase contains RNA, interphase contains DNA, and a lower phase contains proteins. Carefully pipet the aqueous phase and avoid transferring the interphase into the pipette.

Add 0.5 mL of 100% ethanol to the aqueous phase and mix well.

Proceed with the RNA Clean-up protocol of the ZYMO-Spin column.

Subject the cleaved fragment of substrate 1 to the Qsep1 for size distribution analysis, and the cleaved fragment of substrate 2 to gel electrophoresis analysis.

Agilent bioanalyzer (Agilent 2100 Bioanalyzer) with the Agilent RNA Pico Kit (Cat # 5067-1513RUO) can be used instead of Qsep1.

Expected outcomes

Here, we provide an optional protocol to detect AGO1-RISC assembly and cleavage by fluorescent labeling of RNA instead of radiolabeling. We use a FAM-ASO that is complementary to the miR-9b guide strand to detect the mature AGO1-RISC (Figures 7A and 7B). Moreover, we prepare FAM-labeled RNA substrate by T4 RNA ligation and perform the cleavage assay (Figures 7C–7E).

Figure 7

In vitro RISC assembly and cleavage assay

(A) Schematic of AGO-RNA-induced silencing complex assembly.

(B) The lysates from transfected S2 cells treated with dsRNA targeting dcr-2, ago2, r2d2, and ago1 (Figure 6) were incubated with 5′-FAM-labeled and 3′-2′-O-methylated anti-miR-9b ASO complementary to the guide strand of miR-9b for 40 min. Then the complexes were analyzed by native gel electrophoresis.

(C) Schematic of the cleavage assay procedure. The AGO complexes purified by immunoprecipitation cleaved the RNA substrate at a defined position.

(D and E) The AGO1 was immunoprecipitated by anti-AGO1 protein A/G beads from S2 cell lysates and incubated with cleavage substrate 1 or 2 containing a sequence complementary to miR-9b. The cleaved fragment was detected by gel electrophoresis (D) and Qsep1 (E).∗Indicates the signal corresponding to the cleaved substrate.

Limitations

Because this method labels the target RNA of RISC in the in vitro RISC assembly reaction, only the mature AGO1-RISC is detected. This protocol is not applicable to analyzing the dynamic formation of AGO1-RISC complexes. The sensitivity of fluorescent labeling is lower than that of radiolabeling.

Troubleshooting

Problem 1

Low RNAi knockdown efficiency (steps 2 and 4).

Potential solution

Increase the amount of dsRNA used for RNAi. Seed the S2 cells at a lower density. After dsRNA treatment, treat the S2 cells by starvation using a medium without serum for 30 min.

Problem 2

Low yield of the cleavage RNA substrate (step of preparation of substrate RNAs for the cleavage assay).

Increase the reaction time to 4 h or overnight (6–12 h). Increase the amount of template DNA.

Problem 3

There is no signal for AGO1-RISC present in the agarose gel (step 8).

Check the amount and quality of the miR-9b ASO on an agarose gel to ensure it is intact and of the expected size. Extend the reaction time. The reaction temperature can also be adjusted. The temperature is critical for the formation and stability of mature AGO1-RISC complexes.

Problem 4

RNA degradation (step of preparation of substrate RNAs for the cleavage assay).

RNA is highly sensitive to RNases. To avoid RNase contamination, the pipettes, pipette boxes and tube racks are treated with RNase, RNA and DNA Remover (Vazyme); Use the RNase-free 1.5 mL tubes, pipette tips, and H2O even though the buffer or reagent contains RNase inhibitors, the probability of degradation increases with time and temperature. To preserve RNA quality and avoid degradation, keep everything cold and spend no more than 60 min for RNA recovery.

Problem 5

Images of the RISC assembly contain high background (step 9).

The time of in vitro RISC assembly and the loading volumes of the products should be tested. The background might be reduced by a different loading volume or a longer reaction time.

Resource availability

Lead contact

Further information and requests for resources and reagents should be directed to and will be fulfilled by the lead contact, Dr. Dahua Chen (chendh@ynu.edu.cn).

Materials availability

All unique materials generated from this study are available from the lead contact with a complete Materials Transfer Agreement.

Steps	Temperature	Time	Cycles
Denaturation	94°C	2 min	1
Annealing	94°C–22°C	0.1°C/s	1
Incubation	22°C	5 min	1

Reagent	Amount
10 μM miR-9b-S	1 μL
10 μM miR-9b-AS	1 μL
2 × Phanta Mixture	25 μL
ddH2O	N/A
Total	46 μL

Steps	Temperature	Time	Cycles
Initial denaturation	95°C	2 min	1
Denaturation	95°C	15 s	30 cycles
Annealing	56°C	15 s
Extension	72°C	30 s
Final extension	72°C	3 min	1
Hold	4°C	forever

Reagent	Amount
10 μM T7 Primer	2 μL
10 μM SP6 Primer	2 μL
2 × Phanta Mixture	25 μL
ddH2O	N/A
Total	50 μL

Component	Amount
2 × NTP/CAP	10 μL
10 × Reaction buffer	2 μL
Template DNA	∼ 200 ng
Nuclease-free H2O	N/A
Total	20 μL

Component	Amount
Cleavage substrate 1	20 pmol
3′RNA adaptor	40 pmol
10 × T4 RNA ligase buffer	2 μL
10 mM ATP	2 μL
50% PEG 8000	7 μL
RNase inhibitor (40 U/μL)	1 μL
T4 RNA ligase I	1 μL
Nuclease-free H2O	N/A
Total	20 μL

REAGENT or RESOURCE	SOURCE	IDENTIFIER
Antibodies
Rabbit polyclonal anti-dmAGO1. Working dilution: 1:2000	Abcam	Cat# ab5070; RRID: AB_2277644
Rabbit polyclonal anti-Flag. Working dilution: 1:3000	Sigma-Aldrich	Cat# SAB1306078; RRID: N/D
Mouse monoclonal anti-β-Tubulin. Working dilution: 1:1000	Cowin	Cat# CW0098M; RRID: AB_2814800
Bacterial and virus strains
E. coli DH5α	AlpaLife	Cat# KTSM101L
Chemicals, peptides, and recombinant proteins
2 × Phanta Max Master Mix	Vazyme	Cat# P525-01
Protein A/G agarose beads	Thermo Fisher Scientific	Cat# 21186
Lipofectamine 2000	Thermo Fisher Scientific	Cat# 11668019
HEPES	Thermo Fisher Scientific	Cat# 11344041
KOH	Aladdin	Cat# P11287-500g
KAC	Aladdin	Cat# P108329-500g
Nonidet P-40	Thermo Fisher Scientific	Cat# 28324
Glycerol	Thermo Fisher Scientific	Cat# 17904
RNase Free H2O	Solarbio	Cat# R1600
cOmplete Protease Inhibitor Cocktail	Roche	Cat# 4693116001
Triton X-100	Sigma	Cat# X-100
Tween 20	Sigma	Cat# P1379
PageRuler Prestained Protein Ladder, 10–180 kDa	Thermo Fisher Scientific	Cat# 26616
Agarose	Invitrogen	Cat# 16500500
EDTA (Ethylenediaminetetraacetic acid)	Sigma	Cat# 798681
Trizol	TIANGEN	Cat# DP424
SYBR qPCR Master Mix	Vazyme	Cat# Q711
T4 RNA ligase I	NEB	Cat# M0437M
RNase inhibitor	NEB	Cat# M0314L
RNA Loading Dye	NEB	Cat# B0363S
ssRNA Ladder	NEB	Cat# N0364S
Schneider’s Drosophila Medium	Gibco	Cat# 11720-067
Opti-MEM	Gibco	Cat# 31985088
Tris Base	Sigma-Aldrich	Cat# 11814273001
Boric Acid	Sigma-Aldrich	Cat# B0394
PBS	Thermo Fisher Scientific	Cat# 14190144
DTT	Thermo Fisher Scientific	Cat# P2325
Creatine Phosphate	Sigma-Aldrich	Cat# 237911
Creatine phosphokinase	Sigma-Aldrich	Cat# C3755
ATP	Thermo Fisher Scientific	Cat# R0441
GTP	Thermo Fisher Scientific	Cat# R0461
ddH2O	N/A	N/A
Liquid nitrogen	N/A	N/A
Critical commercial assays
FasePure Gel DNA Extraction Kit	Vazyme	Cat# DC301-01
pEASY-Blunt Zero Cloning Kit	TransGen Biotech	Cat# CB501-01
T7 RiboMAX Express Large-Scale RNA Production Kit	Promega	Cat# P1700
HiScript III Reverse Transcriptase	Vazyme	Cat#R302
mMESSAGE mMACHINE kit	Thermo Fisher Scientific	Cat# AM1344
RNA clean and Concentrator-5	Zymo Research	Cat# R1013
RNase, RNA and DNA Remover	Vazyme	Cat# R504
Deposited data
Raw and analyzed data	Mendeley	https://data.mendeley.com/datasets/4gmsw3t82z/1
Experimental models: Cell lines
D. melanogaster cell line S2	(Xia et al., 2010)	N/A
Oligonucleotides
T7 primer	(Gao et al., 2022)	5′-TAATACGACTCACTATAGAACAATTGCTTTTACAG-3′
SP6 primer	(Gao et al., 2022)	5′-ATTTAGGTGACACTATAGGCATAAAGAATTGAAGA-3′
dsRNA(gfp) Forward Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAatggtgagcaagggc-3′
dsRNA(gfp) Reverse Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAggtgcgctcctggac-3′
dsRNA(ago1-3′UTR) Forward Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAaaagtatcgcccctccc-3′
dsRNA(ago1-3′UTR) Reverse Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAtttcctatttgctttcaatt-3′
dsRNA(ago2) Forward Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAagccaaggccaataccaa-3′
dsRNA(ago2) Reverse Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAcagaccgaccagggc-3′
dsRNA(dcr-2) Forward Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGActacgcagcttccatagc-3′
dsRNA(dcr-2) Reverse Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAggcattaccgtcccga-3′
dsRNA(r2d2) Forward Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAatggataacaagtcagccgt-3′
dsRNA(r2d2) Reverse Primer	(Gao et al., 2022)	5′-CTCACTATAGGGAGAttcaatggccgctcgc-3′
RT-rp49 Forward Primer	(Gao et al., 2022)	5′-ATGACCATCCGCCCAGCATAC-3′
RT- rp49 Reverse Primer	(Gao et al., 2022)	5′-CTGCATGAGCAGGACCTCCAG-3′
RT-Ago2 Forward Primer	(Gao et al., 2022)	5′-TCCAGGGCACGGCCAAGCCA-3′
RT-Ago2 Reverse Primer	(Gao et al., 2022)	5′-CGATTGCAACGAGGGAACAT-3′
RT-r2d2 Forward Primer	(Gao et al., 2022)	5′-AGGCATTGCGCAGAAAGAAA-3′
RT-r2d2 Reverse Primer	(Gao et al., 2022)	5′-GCAAGGGAACCAACGATGAA-3′
RT-Ago1 Forward Primer	(Gao et al., 2022)	5′-GGAGATCAAGGGTTTGAAGATCG-3′
RT-Ago1 Reverse Primer	(Gao et al., 2022)	5′-AGTGGGAATGATTGCATCTGAG-3′
RT-dcr2 Forward Primer	(Gao et al., 2022)	5′-TCTAGCCTTGTGGCGAGAAA-3′
RT-dcr2 Reverse Primer	(Gao et al., 2022)	5′-GCCTCAAGGGTATCGGCTAT-3′
3′-RNA adaptor	(Gao et al., 2022)	5′-phosphate-GrUrGrCrUrCrGrArGrUrCrGrCrGrGrCrCrGrCrArArGrGrArArCrArUrUrCrGrGrC-3′-6-FAM.
miR-9b-S	(Gao et al., 2022)	5′-GAACAATTGCTTTTACAGATGCACATATCGAGGTGAACATCACGTACGCATACAGCTAAAATCACCAAAGATCGGTTGGCAGAAGCTAT-3′
miR-9b-AS	(Gao et al., 2022)	5′-GGCATAAAGAATTGAAGAGAGTTTTCACTGCATACGACGATTCTGTGATTTGTATTCAGCCCATATCGTTTCATAGCTTCTGCCAACCGA-3′
Recombinant DNA
pAc5.1-Flag-AGO1	(Gao et al., 2022)	https://doi.org/10.1016/j.molcel.2022.02.035
pAc5.1-Flag-EGFP	(Gao et al., 2022)	https://doi.org/10.1016/j.molcel.2022.02.035
pAc5.1-miR 9b	(Gao et al., 2022)	https://doi.org/10.1016/j.molcel.2022.02.035
Software and algorithms
ImageJ	(Schneider et al., 2012)	https://imagej.nih.gov/ij/download.html
Snap gene	SnapGene	https://www.snapgene.com/try-snapgene/
Other
Dounce homogenizer (with tight pestle)	WHEATON	Cat# 1984-10002
Eppendorf centrifuge	Eppendorf	Cat# 5427R
Eppendorf centrifuge	Eppendorf	Cat# 5910R
Cold room	N/A	N/A
Membrane filter, pore size 0.22 m	Millipore	Cat# GSWP04700
Casting Unit	Tanon	Cat# 180-1600&1808
NanoDrop	Thermo Scientific	Cat# ND-ONE-W
LightCycler®480 Real-time PCR	Roche	N/A
Qsep1-lite	BiOptic	Cat# C100001-L
Tanon-6600 imaging workstation	Tanon	N/A

Lysis buffer for RISC assembly lysates

Reagent	Final concentration	Amount
HEPES-KOH (pH 7.4)	30 mM	1.4298 g
KAC	100 mM	1.9628 g
Mg(AC)2	5 mM	0.1424 g
ddH2O	N/A	N/A
Total	N/A	200 mL

Store at 4°C for 6 months. Filtered buffer can be stored at 4°C for up to one year.

5 × TBE solution

Reagent	Final concentration	Amount
Tris base	445 mM	56.3 g
Boric acid	445 mM	27.6 g
EDTA	10 mM	3.7 g
ddH2O	N/A	N/A
Total	N/A	1000 mL

Store at room temperature (22°C–28°C) for up to 6 months. Filter buffer and avoid RNase contamination.

RISC assembly reaction mixture

Reagent	Final concentration	Amount
KAC	133.3 mM	16 μL of 1 M stock
ATP	3.33 mM	4 μL of 100 mM stock
DTT	30 mM	2 μL of 1 M stock
Creatine monophosphate	83.3 mM	20 μL of 500 mM stock
Creatine phosphokinase	0.1 U/μL	6 μL of 2 U/μL stock
RNase Free H2O	N/A	72 μL
Total	N/A	120 μL

Store aliquots at −80°C for up to one year.

IP lysis buffer

Reagent	Final concentration	Amount
Tris-HCl (pH 7.4)	50 mM	3.028 g
KCl	300 mM	11.183g
EDTA	2 mM	0.372 g
Nonidet P-40	0.5%	5 mL
Glycerol	10%	50 mL
ddH2O	N/A	N/A
Total	N/A	500 mL

Store at 4°C for 6 months, and add DTT to a final concentration of 1 mM immediately before use.

IP washing buffer

Reagent	Final concentration	Amount
Tris-HCl (pH 7.4)	50 mM	3.028 g
NaCl	300 mM	8.766 g
MgCl2	5 mM	0.238 g
Nonidet P-40	0.05%	0.5 mL
ddH2O	N/A	N/A
Total	N/A	500 mL

Store at 4°C for 6 months.

Cleavage reaction buffer

Reagent	Final concentration	Amount
HEPES	150 mM	18 μL of 1 M stock
KCl	200 mM	24 μL of 1 M stock
ATP	3.33 mM	4 μL of 100 mM stock
DTT	10 mM	1.2 μL of 1 M stock
MgCl2	25 mM	6 μL of 0.5 M stock
RNase Free H2O	N/A	66.8 μL
Total	N/A	120 μL

Store aliquots at−80°C for up to one year.

Reagent	Amount
2 × SYBR Green Master Mix	10 μL
100 μM RT-Forward Primer	0.1 μL
100 μM RT-Reverse Primer	0.1 μL
cDNA template	9.8 μL
Total	20 μL

Steps	Temperature	Time	Cycles
Initial denaturation	95°C	30 s	1
Denaturation	95°C	10 s	40 cycles
Annealing/ Extension	60°C	30 s
Melting curve	95°C	5 s	1
	65°C	60 s
	97°C	5 s
Cooling	40	30 s	1

Reagent	Amount
RISC Assembly mixture	3 μL
S2 cell lysates	4 μL
50 nM miR-9b ASO	1 μL
RNase inhibitor	0.5 μL
RNase-free H2O	1.5 μL
Total	10 μL

Reagent	Amount
Cleavage reaction mixture	5 μL
Protein A/G Beads +/- Immunoprecipitated AGO1	10 μL
Cleavage substrate 1 or 2	100 ng
RNase inhibitor	1 μL
RNase-free H2O	N/A
Total	25 μL