SIN-3 as a key determinant of lifespan and its sex dependent differential role on healthspan in Caenorhabditis elegans

Diminished muscle function and decreased lifespan is an outcome of sin-3 deletion in C. elegans

Earlier results from our lab demonstrated that wild-type worms fed with bacteria expressing dsRNA against sin-3 gene show significantly reduced lifespan. We further decided to study the role of sin-3 deletion mutant worms [sin-3(tm1276);him-5(e1490) hereafter referred as sin-3;him-5] in comparison to the isogenic control worms [him-5(e1490) hereafter referred as him-5] on lifespan and muscle function. The lifespan of sin-3;him-5 hermaphrodite worms was significantly reduced with mean and maximum lifespan of 10 and 14 days respectively as compared to 19 and 28 days in him-5 hermaphrodite worms (Figure 1a). In males mean and maximum lifespan observed in sin-3;him-5 was 11 and 16 days respectively as compared to 20 and 30 days in him-5 worms (Figure 1b and Tables S1 and S2).

Figure 1. sin-3 deletion causes reduction in lifespan. Kaplan-Meier survival curve showing the lifespan of sin-3;him-5 (dotted lines) and him-5(e1490) (solid lines) worms in (a) hermaphrodites and (b) males. Both hermaphrodites and males with sin-3 deletion manifest significant reduction in mean lifespan. (c) Movement rate in sin-3;him-5 hermaphrodites is compromised. Body bends are represented as strokes per minute. 20 hermaphrodites per strain were evaluated and the experiment was repeated thrice. (d) Movement rate in sin-3;him-5 males is compromised as compared to him-5 mutant males. Body bends are represented as strokes per minute. 20 males per strain were evaluated and the experiment was repeated thrice. (e) Pictures representing the tracks formed by nematodes of strains mentioned. (ns, non-significant; **p < 0.05; ****p < 0.001 and denotes the comparison with respect to him-5 (e1490); One-way ANOVA performed). The images were captured using Nikon stereoscopic zoom microscope at 5X zoom. Scale is equivalent to 200 pixels.

Like in humans, aging in C. elegans coincides with muscle deterioration, or sarcopenia, which is associated with reduced muscle function [23]. Muscles in C. elegans lack regenerative potential in the adult. Therefore, it offers a unique opportunity to study how different stress insults affect aging in a non-regenerating tissue. Several studies have demonstrated age associated decline in coordinated motility and function during C. elegans aging [24–26]. Since movement is an index of vitality and muscle frailty (a known marker for aging) we decided to look for any locomotory defects arising in the background of sin-3 mutation. In preliminary experiments, we found that nematodes are capable of normal sinusoidal movement till day 10 of adulthood. As C. elegans ages, a dramatic decrease in swimming ability, pharyngeal pumping and maximum movement velocity has been previously reported [10,27] and decline in these physiological behaviours is the hallmark of overall muscle health and indicate muscle frailty with progression in age of C. elegans. Our data demonstrated that movement rate (measured in strokes/minute) of C. elegans harbouring sin-3 deletion was significantly compromised with age in hermaphrodite (57 ± 1.5 strokes/ min) as compared to its isogenic (79 ± 1.2 strokes/minute) and wild-type (85 ± 1.7 strokes/minute) controls at 72 h and is reduced by approximately 50% at 96 h (Figure 1c). Similar results were obtained when wild-type worms were fed dsRNA against sin-3 (Table S2).

Parallel trend was observed in males where the mean strokes per minute were 55 ± 0.6 and 69 ± 2.2 respectively for sin-3;him-5 deletion mutant and him-5 mutant at 72 h; and 46 ± 2.1 and 62 ± 0.3 respectively at 96 h (p < 0.05). Interesting observation was that males of isogenic control worms with genotype him-5 manifested significant reduction in number of body bends/minute as compared to their hermaphrodite counterpart both at 72 and 96 h (Figure 1d and S1a).

Another important assay to determine the muscle health is pharyngeal pumping and surprisingly we did not observe any significant difference in both sin-3;him-5 and him-5 mutants with age (Figure S1b). When tracks formed by the mutant worms w.r.t controls were observed at young adult stage, we found that him-5 and wild-type N2 worms gave perfect sinusoidal track with average crest and trough of 0.19 ± 0.03 mm for him-5 and 0.26 ± 0.02 mm for N2 hermaphrodite. Similar trend was observed for males of him-5 where average crest and trough was measured to be 0.18 ± 0.04 mm. However, due to presence of uncoordinated tracks in both sin-3;him-5 hermaphrodite and males, determination of crest and trough was not possible and the tracks were almost straight (Figure 1e and S1c). Our observations further revealed that him-5 worms were fast moving whereas sin-3;him-5 worms were slow moving with a velocity of 0.25 ± 0.02 mm s^-1 as compared to 0.58 ± 0.05 mm s^-1 in him-5 worms (Figure S1d).

sin-3 deletion causes remarkable differences in physiological parameters in C. elegans

The reproductive ability of the organism may also be a reflection of both the lifespan and healthspan. When we assessed the reproductive ability of sin-3;him-5 worms, we found that the sin-3;him-5 worms demonstrated reduced brood size. The total number of eggs produced by sin-3;him-5 worms in self-progeny were 115.8 +3.48 and the viable eggs were 81.2 + 3.7 as compared to 253.2 + 2.1 total eggs and almost all (252.2 + 2.1) eggs were viable in him-5 worms (Figure 2a and 2b). The number of males in progenies were almost similar whether the hermaphrodites were allowed to mate or self-fertilize in both sin-3;him-5 worms and isogenic control him-5 worms (Figure 2c).

Figure 2. Loss of sin-3 causes reproductive defects in C. elegans. Graphical representation of (a) total number of eggs laid in the entire reproductive span of worms, (b) total number of eggs that were viable and (c) percentage of males in the viable progeny after self-fertilization and mating. (d) Loss of sin-3 causes AVID phenotype defect in C. elegans measured as percentage of worms showing ruptured vulva and protrusion of intestine and uterus. (e-g) Graphical representation for the quantification of red, green and the ratio of red/green for JC-1 staining respectively depicting the hypopolarisation of mitochondrial membrane potential in case in sin-3 deletion in C. elegans (For figure a, b and e-f: ns, non-significant; *p < 0.05; **p < 0.001, ****p < 0.0001 and denotes the comparison with respect to wild-type N2; Two way ANOVA performed # p <0.001 denotes the comparison between sin-3;him-5 and him-5(e1490) Student’s t test performed. For figure (c) and (d) *p < 0.05; **p < 0.001, ****p < 0.0001 two way ANOVA performed).

When the crossed progenies were observed, we found that sin-3;him-5 worms produced 101.8 + 6.1 and the him-5 worms produced 271.2 + 2.1 eggs respectively (Figure S2). The percent hatching of self-progeny and mated worms was observed to be 70% & 73% in sin-3;him-5 and 99% in him-5 worms (Table S3). Similar results were obtained when him-5 worms were fed dsRNAi (Table S2).

Age associated vulval integrity defect (AVID) has been chosen as powerful marker for worm healthspan [28]. It can be defined as loss of vulval integrity; thereby ejection of internal organs occurs causing pre-mature death in C. elegans. These worms are often censored from lifespan experiments as being ruptured worms. Our results clearly show that the sin-3;him-5 worms have increased AVID phenotype at 20 °C when compared to him-5 worms. We observed about 18-20% worms showing AVID phenotype in him-5 worms whereas sin-3;him-5 worms showed 48-50% AVID phenotype at 20 °C (p < 0.05). The percentage of AVID increased with decreasing temperature and were 68-70% in sin-3;him-5 worms as compared to 43-46% in him-5 worms at 15 °C (Figure 2d). Similar observations were made with dsRNAi fed him-5 hermaphrodites (Table S2).

Mitochondrial functioning is compromised in sin-3 deletion mutants

We have previously reported that intracellular oxidative stress is the underlying cause for enhanced autophagy and reduced lifespan [12]. In this study so far, we have observed that the sin-3 mutant worms demonstrate an age associated decline in cuticle integrity, stress tolerance, altered physiological parameters, protein homeostasis, and muscle integrity in addition to reduced lifespan. It is reported that sustained high levels of intracellular ROS cause extensive macromolecular damage which induce p53 dependent apoptosis and affect the lifespan and cause accelerated aging and decline in healthspan [29]. To check the role of ROS if any, in sin-3 mutants, mitochondrial membrane potential was determined using JC-1 staining of worms at young adult and at day 10 of attaining adulthood. The results clearly demonstrated that sin-3;him-5 worms had higher membrane depolarization as evident by the perturbed Red::Green fluorescence intensity as compared to the wild-type N2 and the isogenic control. The mitochondrial defects were presented both by the hermaphrodite as well as the male of the sin-3;him-3 strain (Figure 2g and Figure S3). This was further substantiated by the observation that sin-3;him-5 worms showed significantly reduced total cellular ATP levels in both hermaphrodite as well as male populations at day 10 of adulthood with respect to the isogenic strain (Figure S4).

sin-3 deletion results in cuticle defects in C. elegans

C. elegans have an outer body wall made up of collagen, called the cuticle that encapsulates the entire organism. This cuticle provides protection to the worm from outer environment and is also necessary for movement [30]. To analyze the health of the worm in relation to cuticle integrity, young adult worms grown on NGM plate were observed for first break in the cuticle when suspended in alkaline hypochloride solution. Our results show that sin-3 mutants have defective cuticle when compared to their isogenic controls. The major break in cuticle was observed at 69.6 ± 1.45 s in sin-3;him-5 hermaphrodite worms as compared to 125 ± 2.89 s in him-5 worms. Similarly in males of sin-3;him-5 worm the major cuticle break was at 96.7 ± 2.4 s as compared to 173.77 ± 3.2 s in him-5 worms (Figure 3a and Figure 4). The total disintegration of cuticle was observed at the mean time of 172.6 ± 11.0 s for sin-3;him-5 hermaphrodite worms and 267 ± 6.42 s in him-5 worms; for males the time was 171.33 ± 10.26 s in sin-3;him-5 worms and 312.67 ± 12.70 s in him-5 worms (Figure 3b and Figure 4).

Figure 3. sin-3 mutants have defective cuticle. (a) Graph representing the time in seconds when first major break in the cuticle is observed. (b) Graph representing time in seconds till complete disintegration of the cuticle occurred. (c) Body length of sin-3 mutant worms is longer. Graph representing the body length of nematodes of various strains measured at indicated time after attaining L4 stage (two way ANOVA was performed for all experiments; # p < 0.001 denotes comparison w.r.t him-5(e1490) and ** p < 0.001 represent comparison w.r.t N2).

Figure 4. Cuticle disintegration is rapid in sin-3;him-5 mutants. The representative images depicting time in seconds for first major break in cuticles (second row) till complete disintegration of the cuticle (last row) for sin-3;him-5 hermaphrodites and males as compared to isogenic control him-5(e1490) and wild-type worms.

Since body size shows most noticeable change in the hermaphrodite we further decided to measure the body size as a function of time after young adult stage. Surprisingly the body length of sin-3;him-5 worm was 32% longer than him-5 and N2 worms after 96 h following young adult (YA) stage. Difference in body length was apparent from young adult stage worms where in the body length of him-5 was 15% longer as compared to that of sin-3;him-5 worm (Table S4). Similar observations were recorded in dsRNAi (against sin-3) fed him-5 hermaphrodites (Table S2). The percentage body length increased with time in the sin-3;him-5 hermaphrodites as by 48 h it had increased by 25% from 15% seen in L4 staged worms (Figure 3c and S5). The wild-type and him-5 hermaphrodites too demonstrated an increase in body size with time. The increase in body size stagnated at 72 h after L4 stage in all the worms (Table S4).

Stress tolerance and protein homeostasis is compromised in sin-3 deletion mutants of C. elegans

Clegg and coworkers [31] suggested that there is loss of ability to recover from internal and external stress in elderly people. C. elegans can be used to check the ability to maintain homeostasis in healthy animals which is measured as an organism’s ability to respond to various physiological perturbations [9]. We tested the tolerance of worms to two types of stress i.e. heat and osmotic stress in age synchronized young adult worms. The results demonstrated the isogenic control him-5 hermaphrodite worms showed 50% mortality after 5 h of being subjected to heat stress after acclimatization and 4 h when exposed directly to heat stress (Figure 5b). Wild-type N2 hermaphrodites showed similar trend as that of the him-5 hermaphrodites and showed 50% mortality by 3 h when directly subjected to heat stress while 5 h if acclimatization was done before heat stress (Figure 5a). In contrast, the sin-3;him-5 hermaphrodite worm irrespective of acclimatization (25 °C for 18 h) followed by exposure to 37 °C, showed 50% mortality within 1 h of being exposed to the heat stress (Figure 5d).

Figure 5. Loss of sin-3 causes decline in percentage survival of worms after thermal stress insult. Percentage survival with and without acclimatization at 25 °C of (a) N2 hermaphrodite (b) him-5(e1490) hermaphrodites and (c) him-5(e1490) males. (d) Loss of sin-3 causes decline in percentage survival after thermal stress insult in both hermaphrodites and (e) males (ns, non-significant; * p < 0.05; Student’s t test was performed). (f) Loss of sin-3 causes decline in the survival after osmotic stress insults in the strains indicated when tested on NGM plates with 500mM NaCl. (g)sin-3 deletion causes significant protein carbonylation. Hermaphrodite and males of the indicated strains were subjected to quantification of protein carbonyl content (ns, non-significant; *p < 0.05; **p < 0.001, ****p < 0.0001 and denotes the comparison with respect to wild-type N2; Two way ANOVA performed # p <0.001 denotes the comparison between sin-3;him-5 and him-5(e1490) Student’s t test performed).

We also observed that the sin-3;him-5 males were more resistant to heat stress than hermaphrodites and were able to tolerate the heat stress for 3 h under both conditions (Figure 5e). In any case sin-3;him-5 males were more sensitive compared to their isogenic him-5 control males as latter survived up to 6 h when acclimatized and 4 h when exposed directly to heat stress (Figure 5c).

Another stress to which we exposed the worms to check their ability in maintaining homeostasis was osmotic stress; to that end we exposed the worms to 500 mM NaCl. The sin-3;him-5 worms both hermaphrodite and males were significantly more sensitive to osmotic stress as compared to him-5 and N2 worms. sin-3;him-5 hermaphrodites survived the osmotic stress for 113.4 ± 3.6 s and males survived 129.8 ± 4.3 s as compared to the hermaphrodites and males of him-5 worms surviving 270.8 ± 8.11 s and 323.8 ± 5.24 s respectively (Figure 5f).

Severity, specificity, site of generation and the kind of ROS imposed, determines the primary cellular target of oxidative stress dependent damage. Various kinds of protein modification can be brought about either directly or indirectly through reaction of secondary by products of ROS with amino acids. Methionine and cysteine residues are more prone to attack by almost all ROS species [32]. Indeed sin-3;him-5 hermaphrodite and males show enhanced protein carbonylation (6.3 ± 0.23 nmoles/mg protein and 5.73 ± 0.27 nmoles/mg protein respectively) as compared to him-5 hermaphrodite (3.07 ± 0.07 nmoles/mg protein) and males (2.3 ± 1.25 nmoles/mg protein) and wild-type N2 worms (2.43 ± 1.43 nmoles/mg protein) at YA stage (Figure 5g).

Age associated pigments are accumulated in the sin-3 deletion mutants

Our previous study strongly suggests that intracellular oxidative stress is the underlying cause for enhanced autophagy and reduced lifespan in sin-3 mutants [12]. The enhanced autophagy motivated us to check other age related pigments which may be altered in sin-3;him-5 worms. Nile staining of hermaphrodites and male worms demonstrated both qualitative and quantitative increase in age associated lipid deposition in sin-3;him-5 mutants as compared to that of him-5 and wild-type N2 strain with progressive aging from day1 to day 10 of adulthood (Figure 6a and S6). We also recorded the age associated death pigment lipofuscin and observed increased pigment in sin-3;him-5 hermaphrodite and male as compared to the him-5 isogenic control worms and wild-type N2 strain (Figure 6b and S6) with age.

Figure 6. Enhanced age associated lipid and lipofuscin deposition in the sin-3;him-5mutants (a) sin-3;him-5 hermaphrodite and male as compared to worms from him-5(e1490) and wild-type N2 worms at day one and day ten of attaining adulthood. (b) Enhanced age associated death pigment lipofuscin was observed in the sin-3;him-5 hermaphrodite and male as compared to worms from him-5(e1490) and wild-type N2 worms at day one and day ten of attaining adulthood. Visualization was done using NIKON fluorescence microscope. Magnification 400X, scale: 500 µm. 30 worms per strain were visualized and the experiment was repeated thrice.

C. elegans strains and culture conditions

The strains N2 Bristol (wild-type), sin-3 deletion mutant strain KC565 (sin-3(tm1276)I; him-5(e1490)V), CB4088 him-5(e1490)V and E.coli OP50 were procured from the Caenorhabditis Genetics Center (CGC, University of Minnesota). All strains were maintained as described by Brenner [50]. Briefly, nematode growth media (NGM) was prepared and worms were fed with E. coli strain OP50 at 20 °C unless otherwise stated. For all experiments young adult synchronous population, obtained by bleaching as described previously [12] were used unless otherwise stated. When performing dsRNAi experiments, young adults (P0) were fed with bacteria expressing the desired RNAi and the L3 progeny of the F2 generation were examined. For lifespan analysis and measurement of Age associated vulval integrity defects (AVID) worms were picked and allowed to lay eggs to avoid stress conditions.

Age synchronization

Age synchronization was performed as standardized previously [12]. Briefly, egg-bearing worms fed on OP50 were collected using M9 buffer from NGM plates. Gravid adult worms were bleached/lysed in the bleaching solution, followed by a quick centrifugation at 1300 g. The pellet consisting of worm debris was then washed with M9 buffer at least three times. The eggs so obtained were then resuspended in M9 buffer and the tubes were incubated overnight at 20 °C with fairly vigorous shaking to obtain synchronous L1 worms.

Analysis of lifespan

Adults were hand-picked and transferred to fresh plate seeded with the OP50 bacteria for egg laying. The adult worm was removed after eggs were laid and the plates were incubated to obtain worms at L4 stage. The worms were segregated into hermaphrodite and male worms for the lifespan analysis at 20 °C. In all the experiments, the pre-fertile period of adulthood (L4 stage) was used as t = 0 for lifespan analysis. The animals that ruptured, bagged (exhibited internal progeny hatching), or crawled off the plates were censored from lifespan analysis data. Each lifespan experiment was repeated at least three times with n = 75 to 100 worms per experimental group for both males and hermaphrodites. Kaplan-Meier survival analysis was used to compare the mean lifespan of different treatments and P-values were calculated using the log rank (Mantel-Cox method).

Measurement of AVID

Avid measurements were carried out as previously described [28]. Briefly, gravid adults were placed on NGM plates seeded with E. coli OP50 lawns for egg-laying. Subsequently, adults were removed from the plates, and eggs were allowed to hatch and reach L4 stage. Male worms were removed and the experiment was continued with hermaphrodites. Worms were transferred daily till their reproductive phase and later periodically to prevent starvation and avoid contamination. The AVID state was noted for each hermaphrodite under a stereo zoom microscope (Nikon SMZ1000). Worms that crawled off the plate were not considered.

Disintegration assay

Cuticle disintegration was measured as previously described by Watts and coworkers [51]. Briefly, age synchronized young adult nematodes were placed in 0.5 ml alkaline hypochlorite solution (1% sodium hypochlorite, 0.25 M NaOH) in a 96-well transparent bottom plates and cuticle disintegration was scored the time taken for the first major break in the cuticle. Plates were agitated gently every 20 s during observation. Error bars are plotted as mean ± SEM. For each experiment, fifteen worms were taken and the experiments were repeated at least thrice.

Stress assay

Osmotic stress. Resistance to osmotic stress was assessed as described earlier [52], by transferring age synchronized young adult worms to NGM plates containing 500mM NaCl. Twenty animals per plate were scored for survival every 2 minutes till they showed no movement due to dehydration induced paralysis. Results are plotted as mean ± SEM and statistical significance was calculated using two way ANOVA (P≤ 0.05 was considered significant; Bonferroni test was used for multiple comparison).

Thermo tolerance assay. Thermo tolerance assays were conducted at the indicated temperature (37 °C) and live worms were scored every hour for 6 h. For acclimatization, age synchronized young adult worms were first kept at 25 °C for 18 h before shifting to 37 °C. Plates were initiated with 20-25 adult animals each and were placed in an incubator. All plates were numbered randomly and at least three biological replicates were used and then counted for survival every hour.

For all stress resistance assays, Day 1 young adult worms were used. We used at least three biological replicates with a minimum of 20 worms per replicate.

Estimation of Brood size

Brood size was determined as described by Swain et al. [53]. Briefly, single L4 hermaphrodite animal alone or hermaphrodite with 4 males (for determining the brood size after mating) were placed onto individual plates. The plates were incubated at 20 °C and the worms (P0) were transferred to a new plate (replica-plated) every 24 h until they stopped laying eggs, and the number of eggs was recorded every day. Viable progeny was determined by counting the number of hatched larvae (F1) the day following transfer. The nematode brood size was determined based on the sum of total eggs laid by individual hermaphrodites. Percentage of males in the brood was determined after 72 hours by identifying and counting the number of males in F1 progeny using a Nikon SMZ1000 stereo zoom microscope.

Body length, body width and tracks of young adult worms

To measure the body length, L4 larvae worms with an obvious white crescent surrounding the visible prospective vulva were chosen and picked onto fresh plates and incubated at 20°C for 24 h to develop into young adults. 20 worms were photographed per strain using Nikon SMZ1000 stereoscopic zoom microscope. All length measurements were performed with the free Java image processing program ImageJ [54]. Young adult worms were measured from the nose to the tail tip. The body widths were measured at the position of the vulva, from side to side.

To photograph worm tracks, single young adult worms were moved to new plates containing a one day old bacterial lawn and were left undisturbed for 10 minutes. 20 worms per strain per assay were used and the experiment was repeated thrice.

Movement/Thrashing assay

Body bending thrashing assay was performed as described previously [55]. Briefly, 35 mm diameter sterile NGM agar plates were filled with 1 ml of M9 buffer. Before the start of assay, worms were put on a sterile NGM agar plate without bacteria and allowed to crawl freely to remove the agglomerated bacteria from the worm. After examining visually whether the bacteria were removed, young adult (day-1 adult) worm were put into the buffer and allowed to swim freely for 1 minute to be accustomed to the environment. The observations were similarly recorded for each worm after the indicated time from adulthood. Number of body thrashes was counted for one minute. 20 worms per strain per assay were counted. A movement of the worm that swings its head and/or tail to the same side is counted as one thrash.

Pharyngeal pumping assay

Pharyngeal pumping was recorded everyday along with lifespan from adult day one until death of the worms [56]. The pumping assays were performed on NGM agar plates at room temperature using Nikon SMZ1000 stereo zoom microscope. Pharyngeal pumping was defined as the number of times the terminal bulb of the pharynx contracted over one-minute interval. All pumping rates were measured on a lawn of OP50 bacteria at 20 °C at indicated duration after attaining adulthood. Worms were placed on NGM/OP50 plates and left undisturbed for 1 hour before measuring. 20 worms per strain per assay were observed. The experiment was repeated at least thrice.

ATP assay

The ATP assay was performed as described before, with minor modifications [57]. Age synchronized young adult worms were grown on NGM plates seeded with OP50 and collected for assay. In all, 200 age-synchronized day 10 adult worms of various strains were washed with M9 buffer, treated with four freeze-thaw cycles by dipping in liquid N2. The worms were then homogenized in ATP assay buffer followed by deproteinization using 4M Perchloric acid (Fisher Chemicals, A2296, 70.5% w/w or ̴11.7 M) and 2M KOH (Merck Millipore, CAS: 1310-58-3) method as described in the kit. Samples were then spun at 4 °C, 11,000 g for 10 minutes. A colorimetric/fluorometric ATP assay kit (Abcam, Cambridge, UK, AB83355), which utilizes the phosphorylation of glycerol to generate a product that is easily quantified by fluorometric (Ex/Em = 535/587 nm) methods, was used to quantify ATP contents. ATP concentrations were determined using standard curve derived from fluorescence of known ATP concentrations as per the kit instructions. Microplate fluorescence reader (Tecan infinite M200) was used to measure levels of fluorescence. For normalization, protein levels were determined by BCA protein assay kit (Pierce, Thermo Scientific, Rockford, IL, USA).

Osmotic Avoidance assay:

Age synchronized day 10 adult worms were evaluated for osmotic avoidance behavior (OSM) as described previously [52]. The behavior was quantified as the number of worms that crossed a 2 cm ring of 8M glycerol in 10 minutes. 30 worms per strain were observed and the experiment was repeated thrice.

Nile Red assay

The feeding Nile red assay was conducted by seeding wild-type or mutant age synchronized L1 C. elegans on NGM plates containing E. coli OP50 supplemented with 50 ng/mL Nile red (diluted fresh into 100 mL M9 media per plate from 500 mg/mL stock in acetone and added to the top of E. coli plates and allowed to dry). Worms were synchronized at 20 °C in minimal media to obtain the L1 staged worms. Imaging and quantification was conducted after growth at 20 °C as day one and day ten adults using a Nikon Eclipse E600 microscope fluorescence microscope at 200X. All Nile red analyses were carried out on animals grown at 20 °C. 30 worms per strain were visualized and the experiment was repeated thrice.

Protein carbonylation

Worm homogenate was prepared as described by Sharma et.al., [12] and protein carbonylation was quantified using alkaline DNPH method as previously described [58]. Briefly, for each reaction, 400 µl of DNPH (10 mM in 0.5 M H₃PO₄) (2,4-Dinitrophenylhydrazine, Sigma, D199303) was mixed with 400 µl of protein solution containing 500 µg of protein (obtained by sonication of age synchronized day one young adult worms in PBS). The mixture (800 µl) was incubated in dark at room temperature for 10 minutes followed by incubation with 200 µl of NaOH (6 M) for 10 minutes. The absorbance was read at 450 nm with the UV spectrophotometer (Perkin Elmer, MA, USA). Blank contained 400 µl of 0.5M H₃PO₄ instead of DNPH. Molar absorption coefficient of 21 mM⁻¹ cm⁻¹was used and the carbonyl content was calculated as nanomoles of DNPH incorporated (protein carbonyls) per mg of protein.

JC-1 staining for mitochondrial potential (ΔΨm)

The assay was performed as previously described [59]. Briefly, assay of ΔΨm was performed using JC-1 (5,5′,6,6′-tetrachloro-1,1′,3,3′-tetra-ethyl benzimid-azolylcarbocyanine iodide, catalog no. T-3168, Molecular Probes) dissolved in DMSO at a concentration of one mg/ml. Age synchronized day one and day ten hermaphrodite and males were suspended separately in PBS containing freshly prepared 2% paraformaldehyde and incubated for 20 minutes for fixation, followed by washing with M9 buffer. Samples were subsequently transferred to micro centrifuge tubes containing 1µM JC-1 reagent and incubated at 37 °C in a 5% CO₂ incubator for 45 minutes. Samples were washed and suspended in S basal buffer, placed in 96 well black bottom fluorescence plates. Around 100 worms were used per well per replicate. Measurements of red fluorescence (excitation 550 nm, emission 600 nm) and green fluorescence (excitation 485 nm, emission 535 nm) were performed using a fluorescence plate reader (Tecan, infinite M200). The experiment was repeated thrice.

Age pigment (Lipofuscin) Accumulation

One and ten days old adult worms were transferred onto freshly prepared 2% (w/v) agarose pads for microscopy. Levimasole (1mM) was added to the agarose pads to anesthetize the worms. Images were captured on a Nikon Eclipse E600 fluorescence microscope at 200X magnification. Lipofuscin levels were quantified after the acquired images were converted to 16-bit images, thresholded and subsequently quantified using ImageJ software by determining the average pixel intensity in each worm body. 30 worms per strain were visualized and the experiment was repeated thrice.

Statistical Analysis

All data is expressed as mean ± SEM. Unless otherwise stated all data was analyzed using One-way ANOVA for multiple comparisons. Kaplan-Meier survival analysis was used to compare the mean lifespan of different strains. All histograms were generated and all statistical analysis were performed using GraphPad Prism (GraphPad Software Inc. version 6.01). Bonferroni's multiple comparisons test was employed and P< 0.05 was accepted as statistically significant difference. The results have been expressed as mean ± SEM unless otherwise stated.