An Easy Method for Plant Polysome Profiling

Summary

This protocol describes an easy method to extract and fractionate transcripts from plant tissues on the basis of the number of bound ribosomes. It allows a global estimate of translation activity and the determination of the translational status of specific mRNAs.

Abstract

Translation of mRNA to protein is a fundamental and highly regulated biological process. Polysome profiling is considered as a gold standard for the analysis of translational regulation. The method described here is an easy and economical way for fractionating polysomes from various plant tissues. A sucrose gradient is made without the need for a gradient maker by sequentially freezing each layer. Cytosolic extracts are then prepared in a buffer containing cycloheximide and chloramphenicol to immobilize the cytosolic and chloroplastic ribosomes to mRNA and are loaded onto the sucrose gradient. After centrifugation, six fractions are directly collected from the bottom to the top of the gradient, without piercing the ultracentrifugation tube. During collection, the absorbance at 260 nm is read continuously to generate a polysome profile that gives a snapshot of global translational activity. Fractions are then pooled to prepare three different mRNA populations: the polysomes, mRNAs bound to several ribosomes; the monosomes, mRNAs bound to one ribosome; and mRNAs that are not bound to ribosomes. mRNAs are then extracted. This protocol has been validated for different plants and tissues including Arabidopsis thaliana seedlings and adult plants, Nicotiana benthamiana, Solanum lycopersicum, and Oryza sativa leaves.

Introduction

Protein synthesis is an essential and energetically costly process in all cells ¹. First of all, cells must invest energy in the production of the translation machinery, the ribosomes. For example an actively dividing yeast cell produces as much as 2,000 ribosomes per minute. Such a production requires up to 60% of the total transcriptional activity and up to 90% of the total splicing activity of the cell ². In addition, energy is required for the synthesis of amino acids, aminoacyl-tRNA and peptide bonds. In plants, adding one amino acid to a peptide chain costs from 4.5 to 5.9 molecules of ATP ³. Therefore, it is not surprising that the translation of mRNA to protein is a major site of regulation, particularly when it comes to dealing with changing environmental conditions.

The initiation step of translation, that is the association of a mRNA with the ribosome, is the main target of the regulation of translation⁴. As a consequence of the regulation of translation as well as other post-transcriptional regulatory steps, only 40% of the variations in protein concentration can be explained by mRNA abundance ^5,6. Thus, the study of total mRNA gives relatively poor information about protein abundance. On the other hand, the association of mRNA with ribosomes gives better insight into protein abundance by giving access to those mRNAs involved in translation. Actively translated mRNAs are associated with several ribosomes in structures called polysomes. Conversely, poorly translated mRNAs will be associated with only one ribosome (monosome). Consequently, the translational status of an mRNA can be evaluated by monitoring its association with ribosomes⁷.

This protocol describes the isolation of polysomes from six days old Arabidopsis thaliana seedlings, the subsequent isolation of RNA, and the analysis of the results. Polysomes and monosomes are separated through a sucrose density gradient. Gradients are collected into six fractions. Some of the fractions are pooled to obtain three well separated fractions: polysomes, monosomes and the light fraction (hereafter called supernatant), which contains the free 60S and 40S ribosomal subunits and mRNAs that are not associated with ribosomes. Global translation activity can be estimated by generating a polysome/monosome ratio, which is determined by integration of the area under the curve, and by comparing the polysomes profiles. mRNAs and proteins are then extracted from the different fractions and used for analysis by RT-PCR, qRT-PCR, Northern blot, microarray, western blot or proteomics. This protocol has been validated for other plants and tissues.

The equipment required to perform this protocol are commonly found in most laboratories: There is no need for a gradient maker. Freezing each layer before adding the next one prevents from any mix or disturbance of the layers. No tube piercer is used for gradient collection which can be achieved by immersion of a glass capillary tube in the gradient. Therefore, the costly ultracentrifuge tubes remain undamaged and can be re-used many times. Collectively, this makes the present protocol an easy and cheap method for polysome profiling.

Protocol

1. Preparation of 20 to 50% (w/v) Sucrose Gradients

Note: The gradients are made of 4 layers of sucrose (50%, 35% and 2 layers of 20%) in a 13.2 ml ultracentrifuge tube. In our experience, pouring the 20% sucrose in two separate layers greatly improves the quality of polysome preparations.

1. Prepare the stock solutions. Ensure that all solutions are RNAse and DNAse free.
   1. Prepare 10X Salt Solution: 400 mM Tris-HCl pH 8.4, 200 mM KCl and 100 mM MgCl_2.
   2. Prepare 2 M Sucrose Solution: For 200 ml, dissolve 137 g of sucrose in 1X Salt Solution.
2. Dilute the Sucrose Solution in Salt Solution, as described in Table 1, to prepare the gradients. The volumes given are for six gradients.

Final sucrose concentration	Sucrose 2M (ml)	Salt solution 1X (ml)	Final Vol. (ml)
50%	8.8	3.2	12
35%	12.9	12.1	25
20%	7.4	17.6	25
20%	5.8	14.2	20

Table 1. Dilutions of the Sucrose Solution to prepare six gradients.

3. Pour the layers as per Table 2.

Sucrose layer	50%	35%	20%	20%
Vol. (ml)	1.85	3.65	3.65	1.35

Table 2. Volume of sucrose solution per layer.

4. After pouring each layer, keep the tubes in a -40 °C or -80 °C freezer until complete freezing before adding the next sucrose layer. Freezing is usually achieved after 2 hr at -40 °C, but waiting about 6 hr before pouring the next layer is recommended. The last 20% layer can be frozen or added freshly on the day of the experiment.
   Note: Freezing each layer before adding the next one prevents from any mixing or disturbance of the layers. Gradients can be kept in a -40 °C or -80 °C freezer for at least six months.
5. If it has not already been done, add the last 20% layer to the gradients on the day of the experiment. Then, let the gradients thaw out in a cold room or a fridge.

2. Preparation of Cytosolic Extracts

Note: We recommend using two gradients per biological sample. 300 mg is the optimum amount of plant material to prepare two gradients when working with 6 days old Arabidopsis thaliana seedlings. When working with less translationally active tissues, the amount of plant material can be increased up to 600 mg.

1. Harvest six day old seedlings grown on ½ Murashige and Skoog⁸ medium supplemented with 1% sucrose or equivalent media by quick-freezing in liquid nitrogen
2. Grind plant material in a precooled mortar and pestle with liquid nitrogen.
3. Weigh 300 mg of powdered material in a precooled weighing dish. Perform this step quickly to avoid thawing of the sample.
   Note: Keep the frozen samples for no more than one week in a -80 °C freezer.
4. Add 2.4 ml of precooled polysome buffer (Salt Solution 4X, 5.26 mM EGTA, 0.5% (v/v) Octylphenoxy poly(ethyleneoxy)ethanol, branched, 50 µg.ml^-1 cycloheximide, 50 µg.ml¹ chloramphenicol) and homogenize by mixing with the pipette tip. Transfer into two 1.5 ml tubes. Work quickly to prevent the samples from warming.
5. Centrifuge at 16,000 x g for 15 min at 4 °C in a microcentrifuge to pellet debris.
   Note: To prevent RNA degradation, always keep the samples at 4°C, use RNase/DNase free solutions and work in RNase/DNase free conditions. Heparin can be added to the polysome buffer, to a final concentration of 300 µg.ml^-1, to enhance RNA protection. However, since heparin can interfere with downstream analysis, it will have to be removed during the RNA precipitation step by performing lithium chloride precipitation instead of ethanol precipitation (cf. note 4.7).

3. Polysome Profiling

1. Carefully pipette the supernatant without disturbing the pellet. If plant fragments have been pipetted, repeat step 2.5. Load the supernatant on top of the gradient by gently pipetting onto the sidewall of the tube in a constant stream. Use one gradient for each 1.5 ml tube.
2. Transfer to precooled buckets and centrifuge at 175,000 x g for 2 hr 45 min at 4 °C, in an ultracentrifuge (e.g. 32,000 rpm when using a SW41 rotor).
3. Set up the gradient collection system as described in Figure 1. The UV cuvette has a 1 mm pathlength.

Figure 1. Gradient collection system. The UV cuvette is connected by polyvinyl chloride tubing to a glass capillary tube that descends to the bottom of the gradient. The gradient progresses through the system thanks to a peristaltic pump. OD₂₆₀ is continuously read and 2 ml fractions are collected. Please click here to view a larger version of this figure.

4. Adjust the fraction collector to RT, and set the carousel at a speed that will allow the collection of 2 ml fractions. Use pre-cooled collection tubes.
5. Collect the fractions from bottom to top using a glass capillary tube connected by polyvinyl chloride tubing to the gradient collection system. Use a plastic paraffin film to secure the connection between the polyvinyl chloride tubing and the glass capillary tube.
6. Read the absorbance at 260 nm from the bottom to the top of the gradient. When the entire gradient is collected, place the collection tubes on ice before RNA extraction.

4. RNA Extraction

1. Pool the fractions collected from two gradients, in 50 ml capped centrifuge tubes, as follows:
   Polysomes: fractions 1 to 3 (12 ml)
   Monosomes: fraction 4 (4 ml)
   Supernatant: fractions 5 and 6 (8 ml)
2. To each fraction, add 1 vol. 8M guanidine hydrochloride, 50 µg acryl carrier and 1.5 vol. isopropanol.
   Note: Acryl carrier is linear acrylamide, used as a coprecipitant to improve the recovery of nucleic acids during alcohol precipitation.
3. Mix by inverting the tubes and precipitate O/N at -20 °C.
4. Centrifuge at 175,000 x g for 1 hr at 4 °C, in an ultracentrifuge (32,000 rpm in a SW32 rotor). If the precipitation step is performed in a tube which is not compatible with ultracentrifugation, transfer to a suitable tube.
5. Discard supernatant and dissolve the pellet in 200 µl RNAse-free TE buffer (10 mM Tris-HCl pH 7.5 - 1 mM EDTA). Transfer to a fresh 1.5 ml tube.
6. Extract RNA by adding 1 vol. water saturated phenol (pH 6.6) and 1 vol. chloroform:isoamyl alcohol (24:1). Mix vigorously. Centrifuge at 15,000 x g for 20 min at 4 °C. Transfer the aqueous phase to a new 1.5 ml tube.
   Note: Acid phenol (pH 4.5) can be used in order to minimize DNA contamination.
7. Precipitate RNA by adding 1/10 vol. 3 M sodium acetate and 3 vol. 100% ethanol. Allow precipitation at -80 °C for 20 min or O/N at -20 °C. Centrifuge at 15,000 x g for 15 min at 4 °C.
   Note: If using heparin in the polysome buffer (cf. note 2.5), perform a lithium chloride (LiCl) precipitation instead of ethanol precipitation to properly remove any trace of heparin that could interfere with downstream analysis⁹. After extraction, add LiCl to a final concentration of 2.5 M. Allow precipitation for 30 min at -20 °C or O/N at 4 °C. Centrifuge at 15,000 x g for 15 min at 4 °C.
8. Wash the pellet with 500 µl 75% ethanol. Air dry the pellet and dissolve in 30 µl TE buffer. Assess RNA quality by electrophoresis on an RNAse free 1.2% agarose gel (100V, 15 min) or by capillary electrophoresis methods.

5. Data Analysis

1. Export raw data to a graphic and data analysis software.
   Note: As shown in Figure 2A and B, the raw profiles give qualitative information: the number of polysome peaks that can be seen, the height of the monosome peak, and the presence of a shoulder corresponding to the free ribosome subunits.
2. Merge profiles to allow comparison of the profiles between samples. Use the screen reader tool to determine the X value of the monosome peak for each sample and align the monosome peaks by removing extra data points at the beginning of the curves. Identify the lowest point of the curve and determine its Y value (using the screen reader tool). Set the lowest point Y value to 0 by using the "set columns value" function.
3. Determine the polysomes/monosomes ratio by integrating the area under the curve from raw profiles (Figure 3C). Use the data selector tool to define the border of the area to be integrated. Then use the integrate function (Analysis-Mathematics).
4. Normalize the curves to the monosome peak by dividing all data points of a curve by the Y value of the summit of the monosome peak (determined using the screen reader tool). Select the column, then under Analysis-Mathematics, select Normalize and choose the "divided by a specified value" methods. This step allows comparison of the relative level of polysomes (Figure 3D).

Figure 2. Representative polysome profiles. Arabidopsis thaliana wild-type (wt, ecotype Col-0) and mutant seedlings were grown for six days on ½ Murashige and Skoog medium under long day photoperiods (16 hr light, 8 hr dark). A: raw polysome profiles from wt seedlings. B: raw polysome profiles from mutant seedlings. C: Determination of the percentage of polysomes and monosomes by integration of the area under the curve D:Polysome profiles normalized to the monosome peak. Please click here to view a larger version of this figure.

Results

In the literature, polysome profiles are often shown from the light fraction to the heavy fraction as a result of the way the gradients are collected, i.e. from the top to the bottom. Since in the protocol described here the gradients are collected from the bottom to the top, the profiles we show start with the heavy fraction (the polysomes) and go to the light fraction (free ribosome subunits and RNAs) (Figure 2A). We then collect each gradient in six 2 ml fractions, but...

Discussion

The protocol we present here is an easy and cheap method for generating polysome profiles and isolating mRNAs associated with polysomes, single ribosomes or free of ribosomes. A wide range of different polysome fractionation methods is described in the literature. The method we have described here has been optimized to keep only the necessary compounds and has been adapted for plant material. In particular, we reduced the amount of detergent¹¹ and added chloramphenicol to the buffer to fix the chloroplastic ri...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Ultracentrifuge tube, thinwall, polyallomer - 13.2 ml	Beckman Coulter	331372
Ultracentrifuge tube, thinwall, polyallomer - 38.5 ml	Beckman Coulter	326823
Glass capillary tube	Drummond Scientific	1-000-1000
Ultracentrifuge	Beckman Coulter	Optima series
Ultracentrifuge Rotor SW41	Beckman Coulter	331362
Ultracentrifuge Rotor SW32	Beckman Coulter	369650
Peristaltic pump	Any
Tygon R3607 polyvinyl chloride tubing	Fisher Scientific	070534-22	Polyvinyl chloride tubing, 2.29 mm
Fraction collector Model 2110	Bio-Rad	731-8120
UV cuvette	Hellma	170.700-QS	Quartz flow-through cuvette
UV Spectrophotometer	Varian	Cary50	Read every 0.0125 sec
All chemicals	Any		Use only Molecular Biology Grade
Murashige and Skoog Basal Salt Mixture (MS)	Sigma-Aldrich	M5524
Rnase-Free water	Any
Petri Dishes	Fisher Scientific	10083251
Octylphenoxy poly(ethyleneoxy)ethanol, branched (Nonidet P40)	Euromedex	UN3500
Linear acrylamide (acryl carrier)	ThermoFischer scientific	AM9520	RNA precipitation carrier
OriginPro 8	OriginLab		Analysis software