Tissue-Specific RNAi Tools to Identify Components for Systemic Stress Signaling

Summary

Maintenance of organismal proteostasis requires the coordination of protein quality control responses such as chaperone expression from one tissue to another. Here, we provide tools used in C. elegans that allow monitoring of proteostasis capacity in specific tissues and determine intercellular signaling responses.

Abstract

Over the past decade there has been a transformative increase in knowledge surrounding the regulation of protein quality control processes, unveiling the importance of intercellular signaling processes in the regulation of cell-nonautonomous proteostasis. Recent studies are now beginning to uncover signaling components and pathways that coordinate protein quality control from one tissue to another. It is therefore important to identify mechanisms and components of the cell-nonautonomous proteostasis network (PN) and its relevance for aging, stress responses and protein misfolding diseases. In the laboratory, we use genetic knockdown by tissue-specific RNAi in combination with stress reporters and tissue-specific proteostasis sensors to study this. We describe methodologies to examine and to identify components of the cell-nonautonomous PN that can act in tissues perceiving a stress condition and in responding cells to activate a protective response. We first describe how to generate hairpin RNAi constructs for constitutive genetic knockdown in specific tissues and how to perform tissue-specific genetic knockdown by feeding RNAi at different life stages. Stress reporters and behavioral assays function as valuable readouts that enable the fast screening of genes and conditions modifying systemic stress signaling processes. Finally, proteostasis sensors expressed in different tissues are utilized to determine changes in the tissue-specific capacity of the PN at different stages of development and aging. Thus, these tools should help clarify and allow monitoring the capacity of PN in specific tissues, while helping to identify components that function in different tissues to mediate cell-nonautonomous PN in an organism.

Introduction

Cellular proteostasis is monitored by an intricate network of protein quality control components such as molecular chaperones, stress responses and degradation mechanisms including the ubiquitin proteasome system (UPS) and autophagy^1,2. The activation of stress response pathways, such as the HSF-1 mediated heat shock response (HSR), the unfolded protein response of the endoplasmic reticulum (UPR^ER) and the mitochondria (UPR^mito) is vital for cellular adaptation to and survival during environmental challenges or protein misfolding disease that lead to toxic protein aggregation^1,2,3,4,5,6.

Cellular proteostasis is coordinated by an additional layer in multicellular organisms, such as C. elegans, that requires the orchestration of cellular stress responses across different tissues to activate protective protein quality control components such as molecular chaperones⁷. In the past decade, cell nonautonomous activation of “cellular” stress response pathways has been observed for the heat shock response (HSR), the UPR^ER and the UPR^mito, as well as transcellular chaperone signaling (TCS)^3,4,7,8,9,10. In each case, the nervous system as well as signaling from the intestine plays a crucial role in controlling the activation of chaperones across tissues, to protect against the toxic consequences of acute and chronic protein misfolding stresses^3,5,9,11. This transmission from the neurons to the intestine and other cells in the periphery can be achieved by neurotransmitters as is the case for the UPR^ER and the HSR^6,8,11. In one form of cell nonautonomous stress signaling, TCS, that is activated by the increased expression of HSP-90 in the neurons, secreted immune peptides play a role in the activation of hsp-90 chaperone expression from the neurons to the muscle⁵. In another form of TCS, reducing the expression of the major molecular chaperone hsp-90 in the intestine leads to an increased expression of heat-inducible hsp-70 at permissive temperature in the body wall muscle^5,10. In this particular case, the specific signaling molecules activated in the stress-perceiving intestine and the responding muscle cells are, however, unknown.

Thus, in order to identify how chaperone expression is activated from one tissue to another, an approach is required that allows to monitor the capacity of the proteostasis network (PN) and stress response activation at the tissue-specific level. To investigate which stress response pathway is activated in the individual tissues, an available selection of transcriptional chaperone reporters fused to fluorescent protein tags can be utilized (see also Table 3). These include fluorescently tagged hsp-90, hsp-70 and hsp-16.2 transcriptional reporters that indicate the induction of the HSR, hsp-4 that indicates the activation of the UPR^ER and hsp-6, indicating the UPR^mito. The combination of these reporters with a tissue-specific stress condition then allows a powerful read-out that will pin-point individual tissues responding to an imbalance of the PN in a distal “sender” tissue perceiving the stress. To induce a stress condition or imbalance of the PN in a specific tissue, different approaches can be taken. For example, one such approach is by ectopic expression of the activated form of a stress transcription factor (e.g., xbp-1s) and another one is by reducing the expressing levels of an essential molecular chaperone (e.g., hsp-90) using tissue-specific promoters^8,10. To deplete PN components in only one cell type, tissue-specific knockdown by RNAi is a useful tool.

In C. elegans, RNAi is however systemic; double stranded RNA in the environment can enter and spread throughout the animal to silence a targeted gene^12,13. This systemic spread of ingested dsRNA is mediated by SID (systemic RNAi defective) proteins, such as SID-1 and SID-2 proteins that are dsRNA transporters, as well as SID-5, that colocalizes with late endosome proteins and is implicated in the export of ingested dsRNA^14,15,16. SID-1 is a multi-pass transmembrane protein in all cells except neurons, and is required for dsRNA export as well as import into cells¹⁷. SID-2 expression is restricted to the intestine where it functions as an endocytic receptor for ingested dsRNA from the intestinal lumen into the cytoplasm of intestinal cells¹⁶. Neurons lack a response to systemic RNAi, and this correlates with reduced expression of the transmembrane protein SID-1 in neurons, that is essential for dsRNA to be imported^15,18. Thus, for tissue-specific RNAi to be effective in only one cell-type, the systemic spread of dsRNA needs to be prevented. This can be achieved by utilizing the RNAi-resistant sid-1(pk3321) mutant that prevents the release and uptake of dsRNA across tissues¹⁵. Expression of a tissue-specific hairpin RNAi construct in this mutant or the ectopic expression of SID-1 in a specific tissue can then complement the function of mutant sid-1 and will allow for tissue-specific RNAi¹⁹.

So how is dsRNA ingested by the intestine in a sid-1 loss of function mutant and how can it then reach neurons or muscle cells that ectopically express a SID-1 construct? In one current model explaining this mechanism, endocytosed dsRNA is taken up into the intestinal cytoplasm via SID-2 and then exported into the pseudocoelom by another SID-1 independent mechanism, involving SID-5 and transcytosis¹⁷. Thus because SID-1 is required for dsRNA import¹⁷, only cells expressing wild type SID-1 will be able to take up the dsRNA released from the intestine into the pseudocoelom.

Here we demonstrate the use of a set of tools that allow for tissue-specific RNAi. We use the example of the molecular chaperone Hsp90 to describe the construction of hairpin RNAi that can be useful to constitutively knock down gene expression in a specific tissue¹⁰. The described approach could be used for any target gene of interest. The response of other tissues to the proteostasis imbalance caused by tissue-specific hsp-90 RNAi can be probed by monitoring the expression of fluorescently tagged stress reporters in other tissues. As a second method for tissue-specific RNAi, we demonstrate how the sid-1 mutant system can be adapted for feeding RNAi-expressing bacteria rather than expression of a hairpin RNAi construct. This can be useful when performing a candidate or genome-wide RNAi screen to identify components required for a tissue-specific response. Likewise, developmental defects associated with depletion of a vital PN component will require RNAi-mediated knockdown in specific tissues at later stages of development. We demonstrate how a SID-1 complementation system can be used on a candidate RNAi screen for tissue-specific TCS modifiers. In the example, we aim to identify signaling components that upon knockdown in the “stress-perceiving” sender tissue (intestine) and the stress effecting tissue (muscle) lead to the changed expression of a fluorescently tagged hsp-70 reporter in muscle cells.

Protocol

1. Tissue-specific RNAi in two ways: Hairpin RNAi and tissue-specific SID-1 complementation

1. Generation of hairpin RNAi constructs for tissue-specific expression in sid-1 mutants
   1. Amplify the target gene sequence (e.g., hsp-90 sequence isolated from the hsp-90 RNAi clone from the Ahringer RNAi library²⁰) by PCR. Place a nonpalindromic sequence at the 3’ end of the hsp-90 sequence, that is a SfiI site (ATCTA)²¹.
      NOTE: The primers used for cloning the hsp-90 with the SfiI sequence (underlined) are:
      as-hsp90-SfiI 5’-GGCCATCTAGGCCCTGGGTTGATTTCGAGATGCT-3’
      as-hsp90 5’ TCATGGAGAACTGCGAAGAGC-3’.
   2. Subclone the amplified sequence into the commercial cloning kit vector (e.g., TOPO pCR BluntII).
   3. Isolate the inverted hsp-90 sequence from the hsp-90 RNAi clone (Ahringer RNAi library)²⁰ by restriction digestion using XbaI and PstI restriction sites and place it downstream of the hsp-90-SfiI sequence in the vector (from step 1.1.1), resulting in an hsp-90 hairpin construct (Figure 1).
   4. Subclone the hairpin construct into a Gateway entry vector pDONR221 and fuse it with Gateway entry clones that contain tissue-specific promoters for either expression in neurons (rgef-1p); in the intestine (vha-6p); or the bodywall muscle (unc-54p) and the unc-54 3’UTR (or any other 3’UTR of choice) in a Gateway reaction as described in the protocol of the supplier.
   5. Linearize the resulting hairpin RNAi constructs (Figure 1) using a unique restriction site outside the coding sequence and microinject as a complex array at a concentration of 1 ng/µL hairpin RNAi construct, mixed with 100 ng/µL N2 Bristol genomic DNA (digested with ScaI) into a C. elegans strain expressing the hsp-70p::RFP reporter (strain AM722) and crossed into the genetic background of sid-1(pk3321) mutants (strain NL3321). For a protocol on how to perform microinjection of complex arrays please follow²².
   6. As a negative control, use empty vector hairpin constructs expressing the nonpalindromic SfiI containing sequence (GGCCATCTAGGCC) under control of a tissue-specific promoter.
   7. Use the increased hsp-70p::RFP expression of the reporter as a readout to score positive transformants expressing hsp-90 hairpin RNAi (Figure 3). For a more general approach to verify the tissue-specific knock-down of any gene of interest, measure whole animal mRNA levels using qRT-PCR of the gene of interest.
   8. Integrate the extrachromosomal array of the resulting strain expressing the intestine-specific hsp-90 hairpin construct (PVH2; see Table 1) by gamma-irradiation. For integration of the extrachromosomal arrays into the genome, please see²².
2. Tissue-specific SID-1 expression to allow for tissue-specific RNAi by feeding dsRNA-expressing bacteria
   1. Subclone the sid-1 genomic DNA from vector TU867 (unc-119p::SID-1)¹⁹ into the Gateway entry vector pDONR221. Primers for cloning of sid-1 DNA can be found in¹⁹. Fuse the sid-1 pDONR221 construct with Gateway entry clones containing muscle- (myo-3p) or intestine- (vha-6p) specific promoters and the unc-54 3’UTR (or any other 3’UTR of choice) in the Gateway reaction as described before in 1.1.4.
   2. Microinject the resulting vha-6p::SID-1::unc-54 3’UTR or myo-3p::SID-1::unc-54 3’UTR constructs at a concentration of 30 ng/µL together with a red fluorescent pharyngeal co-injection marker (e.g., myo-2p::RFP; 5 ng/µL) into sid-1(pk3321) mutants.
   3. Integrate the extrachromosomal intestine- or muscle-specific sid-1 arrays into the genome as described in²². Here, this resulted in strains PVH5 [myo-3p::SID-1; myo-2p::RFP];sid-1(pk3321) and PVH65 [vha-6p::SID-1; myo-2p::RFP];sid-1(pk3321).
   4. For neuron-specific expression of sid-1 in the sid-1(pk3321) mutant, use strain TU3401 uIs3401[unc-119p::SID-1; myo-2p::RFP];sid-1(pk3321) that was generated previously by Calixto et al.¹⁹.
   5. As mentioned in 1.1.7, ensure tissue-specific knockdown of the gene of interest by measuring mRNA levels of the desired target gene by qRT-PCR. Alternatively, confirm tissue-specific RNAi sensitivity by using a fluorescent protein (e.g., GFP or RFP) expressed in the same tissue and treat worms with GFP or RFP RNAi. Expose nematodes to GFP/RFP RNAi as synchronized L1 stage larvae and grow on the RNAi bacteria until Day 1 of adulthood (see Figure 2). In our case, we used strains expressing SID-1 in the neurons, muscle or intestine and crossed into strains expressing HSP-90::RFP in neurons (AM987), in the intestine (AM986) and in the muscle (AM988).

2. Using stress reporters and proteostasis sensors to monitor cell autonomous and cell nonautonomous proteostasis

NOTE: To monitor PN capacity in specific tissues, use tissue-specific proteostasis sensors (such as strains expressing Q44 in the intestine or Q35 in the muscle – see Table 3) and stress reporters (such as the heat-inducible hsp-70p::mCherry reporter; Table 3).

1. Genetically crossing the sid-1 (pk3321) mutant allele into a proteostasis sensor strain and confirming the presence of sid-1(pk3321) by feeding RNAi
   1. Genetically cross the proteostasis sensor/stress reporter strain into the genetic background of the sid-1 (pk3321) mutant strain. To establish genetic crosses between different transgenic strains, please follow²³ for a detailed protocol.
      NOTE: sid-1(pk3321) mutants are resistant to feeding RNAi and hence treatment of embryos with RNAi against an essential gene (such as elt-2 or hsp-90) will only lead to developmental arrests or larval lethality in strains heterozygous or wildtype for the sid-1 gene.
   2. Let 10 gravid hermaphrodites lay eggs on RNAi plates against elt-2 or hsp-90 and control (empty vector; EV) RNAi plates at 20 °C. Remove the mothers after 1 - 2 h. Use N2 Bristol and the sid-1(pk3321) mutant as controls.
   3. Observe development of the larvae on the RNAi plates over the next 2-3 days. elt-2 RNAi will result in L1 larval arrest, while hsp-90 RNAi results in L3 larval arrest in N2 Bristol. sid-1 mutants will be unaffected by the RNAi treatment and will develop into gravid adults.
      NOTE: C. elegans homozygote for sid-1(pk3321) will show a uniform population developing into adulthood. Heterozygotes will be indicated by mixed populations of some animals showing larval arrest, and some animals developing into adults.
2. Confirming the presence of sid-1(pk3321) by genotyping
   1. Pick 15-20 worms of the selected candidate F2 strain into a PCR tube containing 15 µL of Worm Lysis Buffer (Table 2).
   2. Place the tube at -80 °C for at least 10 min or overnight.
   3. Incubate the tube in the PCR machine using the following program:
   4. 65 °C for 60 min (lyse worm); 95 °C for 15 min (inactivate Proteinase K); hold at 4 °C.
   5. Use 2 µL of the worm lysate as a “template” to perform the PCR reaction for genotyping, using the following primers for sid-1: sid-1 forw: 5’-agctctgtacttgtattcg-3’ and sid-1 rev: 5’-gcacagttatcagatttg-3’.
   6. Use the following program for PCR genotyping: 1 cycle at 95 °C for 3 min; then 30 cycles of 95 °C for 10 , 55 °C for 30 s, and 72 °C for 30 s; 1 cycle at 72 °C for 10 min, hold at 4 °C.
   7. Purify the ~650 bp PCR product using a PCR purification kit (Table of Materials) and sequence the sid-1 PCR product to identify the G-to-A point mutation of the sid-1 (pk3321) allele. Alternatively, the G-to-A point mutation creates an ApoI restriction site, which can be used on the PCR product for genotyping as described in²⁴.
3. Using iQ44::YFP as a proteostasis sensor for the intestine
   1. Synchronize C. elegans expressing Q44::YFP in the intestine (strain OG412) or crossed into the sid-1(pk3321) mutant background by bleaching, following the protocol described in²⁵. Plate synchronized L1 larvae onto a 9 cm nematode growth media (NGM)-agar plate containing OP50 bacteria and grow until L4 stage at 20 °C.
   2. Collect L4 animals by washing worms off the plate using 5 mL of M9 buffer. Transfer the M9 buffer containing L4 worms to a 15 mL tube using a glass pipette or a siliconized plastic pipette, and centrifuge at 1000 x g for 1 min at room temperature to gently pellet the worms. Remove the supernatant carefully, ensuring to leave the worm pellet undisturbed.
   3. Critical Step: To transfer or plate out nematodes use a glass pipette or a plastic pipette tip that was treated with a siliconizing agent (e.g., SigmaCote) following the manufacturer’s instruction. This prevents the sticking of worms to the plastic surface of a pipette tip.
   4. Repeat step 2.3.2 three more times to wash off all OP50 bacteria from the worms.
   5. Take up the worm pellet in 5 mL of M9 buffer and count the number of worms present in 10 µL.
   6. Plate L4 animals on 6 cm NGM Agar plates containing empty vector control (EV) or hsp-90 RNAi bacteria at a density of 10 worms per plate (prepare 5 plates per time point and biological replicate) and incubate for 24 -48 hours at 20 °C.
   7. After 24 hours (=Day 1 adults) and 48 hours (=Day 2 adults) count the number of Q44 foci in the intestines of nematodes exhibiting aggregates. Score a total of at 30-50 nematodes per biological replicate.

3. Tissue-specific candidate RNAi screen for modifiers of cell nonautonomous proteostasis

NOTE: For the tissue-specific RNAi screen we used strain PVH172 allowing for intestine-specific RNAi by feeding RNAi bacteria and strain PVH171 allowing for muscle-specific RNAi (see Table 1 for genotype).

1. Preparation of the candidate RNAi plates
   1. Prepare 6 cm NGM agar plates supplemented with 100 µg/mL ampicillin, 12.5 µg/mL tetracycline and 1 mM IPTG according to standard methods²⁵.
   2. Use the Ahringer RNAi library to obtain the candidate RNAi clones for the RNAi screen²⁰.
   3. Inoculate 3 mL of LB-amp media (50 µg/mL ampicillin in LB media) in at 15 mL tube with the desired RNAi clone using a plastic pipette tip. Grow at 37 °C overnight with agitation.
   4. The next day add Isopropyl-b-D-thiogalactopyranosid (IPTG) (from a 1 M stock) to a final concentration of 1 mM in the bacterial overnight culture.
   5. Agitate the cultures for a further 3 h at 37 °C.
   6. Plate 300 µL of bacterial RNAi culture onto a 6 cm NGM agar plate supplemented with 100 µg/mL ampicillin, 12.5 µg/mL tetracycline and 1 mM IPTG. Let the plates dry on the bench for 2 days at room temperature, covered with aluminum foil to protect from light. Once dry, the RNAi plates can be stored in a box at 4 °C for several weeks.
2. Synchronization of C. elegans and treatment with RNAi bacteria
   1. To synchronize worm strains, pick 15 gravid adults onto RNAi plates and allow to lay eggs for 1 h. Then remove the adults from the plate.
   2. Critical step: Synchronization by bleaching is avoided in this case, because it can induce the hsp-70p::RFP reporter, as it is a stressful condition for C. elegans.
   3. Pick synchronized L4 stage larvae and transfer to a fresh RNAi plate.
   4. Allow nematodes to grow on the relevant RNAi for two generations to ensure efficient uptake of dsRNA, making sure the temperature is kept at 20 °C.
   5. For imaging and hsp-70p::RFP fluorescence quantification, use Day 1 adults.
3. Preparation of microscope slides
   1. Prepare the microscope slides by placing ~250 µL of a 2% agarose solution (in M9 buffer) onto a glass microscope slide and a second slide place on top to create a flat disc.
   2. Place 5 µL of 5 mM Levamisole solution (in M9 buffer) on the set agarose pad and transfer 5 Day 1 adult worms into the Levamisole drop. Leave the nematodes to paralyze for 5 min.
   3. Once C. elegans are paralyzed, carefully align with a platinum wire pick and remove excess levamisole with a laboratory wipe before addition of a coverslip.
   4. Critical step: Ensure to take images of the worms within 30 minutes after preparation of the microscope slides. Paralyzed nematodes on the microscope slide can dry out and burst, which can compromise the fluorescence measurements.
4. Microscope settings and image analysis
   NOTE: Images are obtained using a confocal microscope equipped with an EM-CCD camera and a microscopy image automation & image analysis software.
   1. Take images at 10x magnifications using a 561 nm laser for RFP fluorescence excitation. Ensure all images are taken using the same settings for laser power, pinhole size and fluorescence gain to enable comparisons.
   2. Save all images as TIFF files.
   3. Perform image analysis using ImageJ. Measure fluorescence intensity in each image as pixels per unit area, with background fluorescence subtracted. Normalize fluorescence intensity for each image to the image area as well as the length of the worms.
   4. Measure the mean intensity using Analyze | Measure in ImageJ. Normalize the resulting intensity value to the image area by dividing the intensity by area.
   5. To normalize the intensity to worm length, measure the worm by drawing a line along the length of the worm in ImageJ and using Analyze | Measure. The reason for normalizing fluorescence intensity to worm length, is that worms can vary in size, dependent on the gene that is knocked down by RNAi, and this could affect the mean intensity.
   6. Normalize the measured fluorescence intensities to untreated controls (i.e., transgenic C. elegans grown on control (EV) RNAi plates). Pool the normalized values to compare mean fluorescence intensities for each RNAi condition. Aim to image 20 worms per biological replicate and collect at least 3 biological replicate images.
   7. Calculate P-values of the mean fluorescence intensity values using student’s t test and perform a correction for multiple testing using the Benjamini-Hochberg method, using a false discovery rate of 0.05.

Results

Tissue-specific RNAi in two ways: Expression of hairpin constructs or tissue-specific SID-1 complementation
Expression of tissue-specific hairpin RNAi constructs allows for constitutive knockdown of a gene throughout development. However this can sometimes be impractical when the surveyed gene is required for organogenesis of that particular tissue, such as elt-2 which is required for development of the intestine²⁶. Tissue-specific SID-1 expression in the RNAi-resista...

Discussion

The methods described here demonstrate the use of tools that allow for the tissue-specific knockdown of PN components in a constitutive and temporal manner. We have previously identified TCS, a cell nonautonomous stress response mechanism that is induced by tissue-specific alteration of Hsp90 expression levels¹⁰. Tissue-specific knockdown of hsp-90 by expression of hairpin RNAi leads to cell nonautonomous upregulation of protective hsp-70 chaperone expression in distal tissues, t...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Ampicillin	Merck	A0166-5G	Protocol Section 3.1.
DNA Clean & Concentrator-500	Zymo Research	D4031	Protocol Section 2.2.
IPTG Isopropyl-β-D-thiogalactoside	Merck	367-93-1	Protocol Section 3.1.
Multisite Gateway Cloning Kit	Thermo Fisher	12537100	Protocol Section 1.2.
SigmaCote	Merck	SL2-25mL	Protocol Section 2.3.
Tetracycline	Merck	T7660-5G	Protocol Section 3.1.
Zero Blunt TOPO PCR Cloning Kit	Thermo Fisher	K280002	Protocol Section 1.1.