Genetic analysis of daf-18/PTEN missense mutants for starvation resistance and developmental regulation during Caenorhabditis elegans L1 arrest

Abstract Mutations in the well-known tumor suppressor PTEN are observed in many cancers. PTEN is a dual-specificity phosphatase that harbors lipid and protein-phosphatase activities. The Caenorhabditis elegans PTEN ortholog is daf-18, which has pleiotropic effects on dauer formation, aging, starvation resistance, and development. Function of 3 daf-18 point-mutants, G174E, D137A, and C169S, had previously been investigated using high-copy transgenes in a daf-18 null background. These alleles were generated based on their mammalian counterparts and were treated as though they specifically disrupt lipid or protein-phosphatase activity, or both, respectively. Here, we investigated these alleles using genome editing of endogenous daf-18. We assayed 3 traits relevant to L1 starvation resistance, and we show that each point mutant is essentially as starvation-sensitive as a daf-18 null mutant. Furthermore, we show that G174E and D137A do not complement each other, suggesting overlapping effects on lipid and protein-phosphatase activity. We also show that each allele has strong effects on nucleocytoplasmic localization of DAF-16/FoxO and dauer formation, both of which are regulated by PI3K signaling, similar to a daf-18 null allele. In addition, each allele also disrupts M-cell quiescence during L1 starvation, though D137A has a weaker effect than the other alleles, including the null. Our results confirm that daf-18/PTEN is important for promoting starvation resistance and developmental arrest and that it is a potent regulator of PI3K signaling, and they highlight challenges of using genetic analysis to link specific DAF-18/PTEN enzymatic activities to particular phenotypes.

The sole Caenorhabditis elegans PTEN ortholog DAF-18 shares significant sequence identity with its human counterpart in the phosphatase and C2 domains (Ogg and Ruvkun 1998;Mihaylova et al. 1999;Fig. 1a). daf-18 regulates longevity, formation of dauer larvae in response to adverse conditions (high population density, low nutrient availability, and other forms of stress), and developmental arrest and survival of starved L1-stage larvae (L1 arrest), each of which is also regulated by PI3K signaling (Murphy and Hu 2013;Baugh and Hu 2020). PTEN transgenes can rescue daf-18 dauer formation defective (Daf-d) and shortened-lifespan phenotypes (Solari et al. 2005), suggesting functional conservation.
Given sequence and functional homology, researchers have fruitfully translated findings between C. elegans and mammals. In addition, research in C. elegans has taken advantage of daf-18 mutations that correspond to the aforementioned PTEN mutations in an effort to connect specific enzymatic activities to specific phenotypes.daf-18(G174E) is the C. elegans homolog of PTEN(G129E), and it is presumed to specifically disrupt lipidphosphatase activity (Fig. 1a). Transgenic expression of daf-18(G174E) is unable to rescue the daf-18 Daf-d, shortened-lifespan, and L1 arrest-defective (Q-cell division) phenotypes, but it can weakly rescue the vulval-induction phenotype (Solari et al. 2005;Nakdimon et al. 2012;Zheng et al. 2018b). These results suggest that lipid-phosphatase activity is important for DAF-18 to regulate dauer formation, aging, developmental arrest, and to a lesser extent vulval induction, and that protein-phosphatase activity may be required to inhibit vulval induction.
Here, we present phenotypic analysis of daf-18(G174E), daf-18(D137A), and daf-18(C169S) in the context of L1 arrest, with focus on starvation resistance. Our initial objective was to identify which DAF-18 enzymatic activities are required for starvation resistance, but we were also concerned about the specificity of each allele with respect to enzymatic activity. Rather than relying on transgenes, we used CRISPR-Cas9 genome editing to modify the endogenous daf-18 locus to produce daf-18(G174E), daf-18(D137A), and daf-18(C169S) mutants. We used 3 (a) (b) Fig. 1. Schematic of DAF-18 protein and experimental design. a) DAF-18 full-length protein sequence was subjected to domain prediction using InterPro (Blum et al. 2021). A dual-specificity lipid/protein-phosphatase domain homologous to that of PTEN and a tensin-type C2 domain that can mediate Ca 2þindependent membrane recruitment of proteins (Lee et al. 1999) are indicated. Three C-terminal amino acids (TKV) constitute a PDZ-binding motif (PDZbm) in PTEN (Kim et al. 1995;Songyang et al. 1997;Steck et al. 1997), but that motif is not conserved in DAF-18 (IYL), though DAF-18 can bind PDZ . The 3 daf-18 missense alleles analyzed in this study are also indicated along with the homologous PTEN mutants. The same color-coding scheme for these alleles is used throughout the figures. b) Well-fed gravid adult worms of different genotypes were hypochlorite treated to obtain embryos, which were immediately placed in starvation cultures to hatch and enter L1 arrest (for experimental details, see Materials and methods). Time points of different assays performed are indicated with each color representing one assay.
complementary assays for L1 starvation resistance: L1 starvation survival, growth during recovery from L1 starvation, and fecundity following L1 starvation (Fig. 1b). We also assayed M-cell divisions and DAF-16::GFP nucleocytoplasmic localization during L1 arrest as well as high-temperature dauer formation with daf-2/ IGFR RNAi. All 3 alleles behaved similar to a daf-18 null mutant in each assay with the exception of the M-cell division assay. To address potential overlapping effects of each mutation on DAF-18 enzymatic activity, we assayed starvation resistance of trans-heterozygotes of D137A and G174E, and these alleles did not complement each other. This result suggests that at least one of the 2 alleles appreciably disrupts both enzymatic activities, confounding the ability to infer causal relationships between a specific enzymatic activity and a specific phenotype. Similar results and conclusions were drawn in a study by Wittes and Greenwald (submitted in parallel) examining somatic gonad and germ-cell quiescence in dauer larvae. Collectively, these 2 studies suggest the need for caution in interpreting results of genetic analysis using these missense alleles.

Strains used in this study
Wild-type strain N2 is from the Sternberg Lab collection.
IC166 daf18(ok480) IV was obtained from the Chin-Sang Lab at Queen's University.

Starvation survival
All strains assayed in this study were maintained on Escherichia coli OP50 nematode growth medium (NGM) plates and were wellfed for at least 3 generations before being used in experiments. Worms were grown and starved at 20 C. Gravid adult worms were hypochlorite treated ("bleached") to collect embryos, which were then resuspended, washed, and cultured in S-basal (including 0.1% EtOH). Cultures had 1 embryo/ml in 5 ml and were placed in 16 mm glass tubes on a tissue-culture roller drum at 20 C so they hatch and enter L1 arrest (Hibshman et al. 2021). The day after hypochlorite treatment, and again every day after that, a 100 ml aliquot of each starvation culture was plated on a 6 cm NGM plate around an E. coli OP50 lawn in the center. The number of larvae in the aliquot was recorded (total plated). Two days later, the number of live worms on the lawn was recorded (total alive). Proportion alive was determined as total alive divided by total plated.

Growth rate measurement
Strains were treated as described above in "Starvation survival," and the same worm population was used both here and in the survival assay. Worms were grown at 20 C. Five hundred microliters of starvation culture was plated on 10 cm NGM plates seeded with E. coli OP50 to support larval development (recovery plates). For the control condition (no starvation), embryos were plated directly after hypochlorite treatment, before starvation cultures were placed on the roller drum. For the starved condition, 500 ml of the starvation culture was plated 4 days after hypochlorite treatment. Worms were washed off plates with S-basal and transferred to unseeded (no OP50) 10 cm NGM plates for imaging using ZEISS SteREO Discovery.V20. Because L1 larvae take 12 h to hatch following hypochlorite treatment, control and starved worms were imaged 60 and 48 h after plating, respectively. This approach enabled measurements of body length after 48 h of feeding for both populations. The image-analysis program WormSizer was used to determine worm length (Moore et al. 2013).

Total brood size measurement
Strains were treated as described above, and the same worm population was used as for growth rate measurement and for starvation survival. Worms were grown at 20 C. For the control condition (no starvation), 18 worms were singled out per genotype from the control recovery plate of the growth-rate assay onto 6 cm NGM plates seeded with OP50 the day after hypochlorite treatment. For the starved condition, a 50 ml aliquot of the starvation culture was plated on a 6 cm NGM plate with OP50 24 h after hypochlorite treatment (12-h starvation) for each genotype, and 18 worms were singled out onto 6 cm NGM plates with OP50 the next day. Starting the day after singling out, and every day after for 5, each worm was transferred to a new 6 cm NGM plate with OP50. The total brood size of each worm was determined from the number of progeny on each plate. Worms that died during the process, including due to internal hatching ("bagging"), were recorded, and their total brood sizes were included in the reported results since gonad abnormalities and bagging are consequences of L1 starvation (Jordan et al. 2019).

M-cell division
Strains were treated as described above in "Starvation survival." Three days after hypochlorite treatment, larvae were mounted on 4% Noble agar pads on microscope slides and covered by a glass cover slip to be examined for M-cell division at 200x total magnification on a Zeiss Axio Imager A1. 100 L1 larvae were scored for each condition in each replicate.

DAF-16::GFP localization
Strains were treated as described above in "Starvation survival." Eighteen hours after hypochlorite treatment (6 h of starvation), a 700 ml aliquot of the starvation culture was centrifuged in a 1.7 ml Eppendorf tube at 3,000 rpm for 30 s to pellet L1 larvae. 1.5 ml of worm pellet was pipetted into the center of a slide with a 4% Noble agar pad, and a glass cover slip was immediately placed on top. A timer was set for 3 min, and the slide was systematically scanned with each individual worm scored for nucleocytoplasmic localization specifically within intestinal cells at 1000x on a Zeiss Axio Imager A1. At least 50 larvae were scored per replicate. Nucleocytoplasmic localization of DAF-16::GFP was scored in intestinal cells and assigned to one of 4 categories: nuclear, more nuclear, more cytoplasmic, and cytoplasmic. "More nuclear" and "more cytoplasmic" are intermediate categories between nuclear and cytoplasmic, with localization being more nuclear or cytoplasmic, respectively. Scoring for each slide stopped after 3 min in order to avoid confounding effects of the worms being mounted on slides.

Dauer-formation assay
Single E. coli HT115 colonies carrying pAD12 for empty vector (EV) or pAD48 for daf-2 RNAi grown on 12.5 mg/ml tetracycline and 100 mg/ml carbenicillin LB plates at 37 C were inoculated into LB starter cultures with the same concentration of tetracycline and half the concentration of carbenicillin. Starter cultures were incubated overnight at 37 C with shaking and then used to inoculate larger cultures of terrific broth (TB) with 25 mg/ ml carbenicillin which were incubated overnight at 37 C with shaking. Cells from large cultures were spun down and resuspended at a final density of 250 mg/ml in S-complete with 15% glycerol. Aliquots were frozen and thawed only once and seeded onto 6 cm NGM plates containing 25 mg/ml carbenicillin and 1 mM IPTG. Lawns were allowed to grow overnight at room temperature before plating worms. For each genotype and each replicate, 7 L4 worms were picked onto EV or daf-2 RNAi plates and grown at 27 C. Twenty hours after plating, they were removed but their progeny were allowed to continue growing at 27 C. Forty-eight hours later, the total number of worms and the number of dauers were recorded for each plate and the proportion of dauers was calculated. Dauers were identified by visual inspection on plates (relatively long, slender shape), and worms that had bypassed dauer formation had vulvas and were typically adults.

Results
daf-18(G174E), daf-18(D137A), and daf-18(C169S) are starvation-sensitive We used CRISPR-Cas9 to edit the laboratory reference N2 genome, producing daf-18(G174E), daf-18(D137A), and daf-18(C169S) mutants (Fig. 1a). We backcrossed these mutants 4 times, and we assayed L1 starvation resistance along with wild type and a null allele of daf-18 (ok480). The ability to survive starvation is clearly an indication of starvation resistance, but L1 starvation also affects growth and reproductive success after recovery, and there are genotypes and conditions that affect growth and fecundity following starvation without appreciably affecting starvation survival (Baugh and Hu 2020). We therefore assayed starvation survival as well as growth and total brood size after recovery (Fig. 1b). Because DAF-18 promotes DAF-16 activity via its wellestablished antagonism toward PI3K signaling, and daf-16 mutants are starvation-sensitive, daf-18(G174E) (presumed lipidphosphatase defective) and daf-18(C169S) (presumed both phosphatase-activities defective) were expected to be starvationsensitive. In contrast, it was unclear whether daf-18(D137A) (presumed protein-phosphatase defective) would affect starvation resistance. We found that all 3 missense alleles of daf-18 are very sensitive to L1 starvation. All 3 mutants and the null mutant survived L1 starvation for a significantly shorter time than wild type (Fig. 2, a and d). Likewise, all 4 daf-18 mutants displayed significantly greater decreases in growth after 4 days of L1 starvation compared to wild type (Fig. 2, b and e). Furthermore, all 4 mutants showed significant reduction in fecundity after 12 h of L1 starvation (Fig. 2, c and f). This last result demonstrates a striking cost of starvation on reproductive success in daf-18 mutants, given little to no effect of this brief 12-h starvation on the wild-type control. Together, these results demonstrate that daf-18(G174E), daf-18(D137A), and daf-18(C169S) are each very sensitive to L1 starvation (based on 3 different assays) comparable to a null allele.
M cells divide in daf-18(G174E), daf-18(D137A), and daf-18(C169S) during L1 arrest In addition to adapting to survive and recover from L1 starvation, wild-type worms remain in a developmentally arrested state while starved. There is a single M mesoblast cell at hatching, and it divides approximately halfway through the first larval stage in fed worms and goes on to produce 18 descendants by the L1 molt (Sulston and Horvitz 1977). However, the M cell does not divide during L1 starvation in wild-type worms (Baugh and Sternberg 2006;Kaplan et al. 2015). Developmental arrest, like starvation resistance, is affected by daf-18, so we assayed M-cell divisions in starved L1 larvae. We scored the number of M cells using an hlh-8p::GFP reporter (Harfe et al. 1998) in daf-18(G174E), daf-18(D137A), and daf-18(C169S), as well as daf-18(ok480) and wild type, after 3 days of starvation (Fig. 1b). M-cell quiescence requires daf-18 and daf-16, and so, by the same reasoning as for starvation resistance, we expected daf-18(G174E) (presumed lipid-phosphatase defective) and daf-18(C169S) (presumed both phosphataseactivities defective) to have M-cell divisions, but it was unclear whether daf-18(D137A) (presumed protein-phosphatase defective) would affect M-cell arrest.
We found that all 3 missense alleles and the null allele of daf-18 display M-cell divisions during L1 starvation (Fig. 3, a and b). However, unlike starvation resistance, daf-18(D137A) (presumed protein-phosphatase defective) was clearly different than the other alleles, with significantly fewer animals with a divided M cell, though still significantly more than wild type (zero). These results show that each of the daf-18 missense mutations confers an L1 arrest-defective phenotype, but they also reveal a difference in penetrance among the alleles.
DAF-16/FoxO localizes to the cytoplasm during starvation in daf-18(G174E), daf-18(D137A), and daf-18(C169S) Though it is possible that DAF-18 regulates L1 starvation resistance and developmental arrest through its putative proteinphosphatase activity, we grew concerned about the specificity with which the D137A and G174E alleles disrupt protein and lipid-phosphatase activities, respectively. We decided to look at a direct target of AGE-1/PI3K signaling, DAF-16/FoxO, at the subcellular level. When insulin/IGF signaling is low, such as during starvation, DAF-16 localizes to the nucleus to regulate transcription, but when insulin/IGF signaling, and thus AGE-1/PI3K signaling, is activated, DAF-16 localizes to the cytoplasm where it is inactive (Henderson and Johnson 2001;Lee et al. 2001;Lin et al. 2001). We expected disruption of DAF-18 lipid-phosphatase activity to render DAF-16 more cytoplasmic during starvation as a result of increased AGE-1/PI3K signaling, but we reasoned that it is much less likely that disruption of its protein-phosphatase activity would affect localization.
We scored DAF-16 subcellular localization after 6 h of L1 starvation (Figs. 1b and 4a). The vast majority of wild-type larvae had DAF-16::GFP localized to the nucleus (Fig. 4, b and c), as expected. In contrast, the vast majority of larvae had DAF-16::GFP localized to the cytoplasm in daf-18(G174E), daf-18(D137A), daf-18(C169S), and daf-18(ok480). These results demonstrate that all 3 missense alleles as well as the null allele have a strong effect on DAF-16::GFP localization. It is a formal possibility that DAF-18 regulates DAF-16 localization independent of AGE-1/PI3K signaling through its protein-phosphatase activity, but we believe the simplest interpretation of these results is that the D137A allele (c) (f) Fig. 2. daf-18 mutants are sensitive to L1 starvation. a and d) Survival was scored daily during L1 arrest, and survival curves were fit using logistic regression. Four biological replicates were performed. For each genotype and each replicate, quasi-binomial logistic regression was performed with the response variable being proportion alive and the explanatory variable being duration of L1 starvation. Half-lives (time corresponding to when the proportion alive is half of the starting value) were estimated by regression and were subjected to Bartlett's test, which indicated homogeneity of variance across all genotypes. Two-tailed unpaired t-tests with variance pooled across genotypes were performed on half-lives to calculate P-values for comparisons between genotypes. b and e) Body length after 48-h recovery on 10 cm NGM plates with E. coli OP50 for food was measured using the program WormSizer for image analysis (Moore et al. 2013) for starved (4-day L1 starvation) and control (no starvation) conditions. Four biological replicates were performed. C and F) Total brood size was scored for each worm in starved (12-h L1 starvation) and control (no starvation) conditions. Three biological replicates were performed. b, c, e, and f) A linear mixed effects (lme) model was fit to the data with the response variable being body length or brood size, fixed effects being the interaction between starvation and genotype, and the random effect being replicates. P-values for interaction terms were extracted. Horizontal bars represent estimates calculated by lme models. D values are differences between estimates in starved and control conditions. Each dot represents an observation with a single worm. d-f) *P < 0.05; **P < 0.01; ***P < 0.001; n.s. not significant.
(presumed protein-phosphatase defective) lacks specificity and also disrupts the lipid-phosphatase activity of DAF-18.
daf-18(G174E), daf-18(D137A), and daf-18(C169S) are dauer-formation defective Insulin/IGF and AGE/PI3K signaling is also a critical regulator of dauer formation (Hu 2007;Murphy and Hu 2013), and the dauer formation constitutive (Daf-c) phenotype of daf-2/IGFR mutants is suppressed by disruption of daf-18 (Mihaylova et al. 1999). We reasoned that in dauer-forming conditions provided by high temperature (27 C) and daf-2/IGFR RNAi, disruption of DAF-18 lipidphosphatase but not protein-phosphatase activity would rescue DAF-2/IGFR signaling and reduce dauer formation. We found that less than 10% of wild-type worms grown at high temperature without RNAi (control conditions) developed into dauer larvae, and that over 30% of worms grown at high temperature with daf-2 RNAi (dauer-forming conditions) became dauers, as expected.
In contrast, no daf-18(G174E), daf-18(D137A), or daf-18(C169S) worms became dauers in either control or dauer-forming conditions (Fig. 5). These results demonstrate that all 3 daf-18 missense alleles suppress dauer formation in response to reduced insulin/ IGF signaling and high temperature. Notably, Wittes and Greenwald (submitted in parallel) also report that daf-18(D137A) (presumed protein-phosphatase defective) is defective at dauer development while focusing on somatic gonad development and germ cell proliferation in dauer larvae induced by daf-7/TGF-b mutation. As for the other phenotypes we examined, it is possible that DAF-18 regulates dauer formation through an unknown mechanism involving its protein-phosphatase activity, but these results along with those of Wittes and Greenwald (submitted in parallel) challenge the notion that D137A disrupts DAF-18 protein-phosphatase activity without appreciable effects on its lipidphosphatase activity.
daf-18(D137A) and daf-18(G174E) do not complement each other The results presented thus far suggest that either DAF-18 affects a variety of phenotypes through its protein-phosphatase activity in addition to its better-characterized lipid-phosphatase activity, or that daf-18(D137A) actually disrupts the lipid-phosphatase activity rather than being selective for the protein-phosphatase activity. We reasoned that by analyzing D137A/G174E trans-heterozygotes we could assess whether these 2 alleles have overlapping effects on DAF-18 function or if they are actually specific to each enzymatic activity. That is, if these alleles are truly specific, then they should complement each other and trans-heterozygotes should be wild-type-like. We produced daf-18(D137A/ G174E) trans-heterozygotes (Fig. 6a), and we assayed their effect on L1 starvation resistance (Fig. 1b) along with homozygous mutants and wild type. We chose starvation resistance since this is our primary focus and we have the most data on this trait. However, our starvation survival and growth assays require large numbers of animals, and we were not able to obtain enough cross-progeny (trans-heterozygotes) for both assays. We found that growth of daf-18(D137A/G174E) animals was more impaired after 4 days of starvation than wild-type (Fig. 6, b and d), suggesting starvation sensitivity. Likewise, daf-18(D137A/G174E) animals produced fewer progeny than wild type after 12 h of starvation (Fig. 6, c and e). Not only were the trans-heterozygotes significantly different from wild type in both assays, but they were statistically indistinguishable from each homozygous mutant in each assay. These results clearly demonstrate that D137A and G174E do not complement each other, suggesting overlapping effects on DAF-18 function.

Discussion
We used genome editing to produce daf-18(G174E), daf-18(D137A), and daf-18(C169S) alleles, and we determined their effects on starvation resistance and developmental quiescence during C. elegans L1 arrest. We hoped to use these missense alleles to dissect the enzymatic activities of DAF-18/PTEN, delineating the function of its lipid and protein-phosphatase activities with respect to some of its mutant phenotypes. We found that all 3 alleles reduced starvation resistance, eliminated nuclear localization of DAF-16::GFP during starvation, and suppressed dauer formation. In each case, penetrance was comparable to a null allele (except a null allele was not included in the dauer-formation assay). Each missense allele also caused an L1 arrest-defective phenotype (M-cell divisions), though penetrance varied, with D137A (presumed protein-phosphatase defective) displaying significantly lower penetrance. There is ample evidence that DAF-18 affects each of these phenotypes through its lipid-phosphatase activity, but there is no evidence that its protein-phosphatase activity is involved, though it is possible that DAF-18 dephosphorylates a protein in the AGE-1/PI3K pathway (Shi et al. 2014). We therefore analyzed trans-heterozygotes of D137A and G174E, and these mutants failed to complement each other's starvationsensitive phenotypes. Together these results suggest that D137A (presumed protein-phosphatase defective) and possibly G174E (a) (b) Fig. 3. daf-18 mutants have M-cell divisions during L1 starvation. a) Proportion of starved L1 larvae with more than one M cell after 3 days of L1 arrest. Three biological replicates were performed. One hundred larvae were scored per genotype per replicate. Horizontal bars represent average proportions. b) Bartlett's test was performed on proportion divided, which indicated heterogeneity of variance across all genotypes. One-tailed unpaired t-tests (without pooling variance across genotypes) were conducted to compare daf-18 mutants to wild type. Two-tailed unpaired t-tests (without pooling variance across genotypes) were conducted to compare between daf-18 mutants. *P < 0.05; **P < 0.01; n.s. not significant.
(presumed lipid-phosphatase defective) disrupt more than one of these 2 DAF-18 activities. Either allele could also affect DAF-18 expression levels, but we cannot distinguish between these possibilities with genetic analysis alone. Wittes and Greenwald (submitted in parallel) analyzed dauer development in D137A/G174E trans-heterozygotes and also observed lack of complementation. They also showed that daf-18 is not haplo-insufficient. These results further suggest overlapping effects of each allele on DAF-18 function, and they also concluded that these alleles do not specifically disrupt one or the other enzymatic activity of DAF-18.
In vitro and in vivo phosphatase assays performed with PTEN greatly outnumber those performed with DAF-18. In vitro experiments actually suggest that PTEN(D92A) has disrupted lipidphosphatase activity (Lee et al. 1999;Xiao et al. 2007;Rodr ıguez-Escudero et al. 2011) in addition to loss of protein-phosphatase activity ). In addition, in vitro and in vivo studies suggest that although PTEN(G129E) retains little lipid- Fig. 4. DAF-16 localizes to the cytoplasm during L1 starvation in daf-18 mutants. a) Representative images of each of 4 categories of DAF-16::GFP nucleocytoplasmic localization in intestinal cells taken at 1,000x. Additional cells are also visible in the images but were not evaluated during scoring. Arrows and arrowheads annotate representative cells with cytoplasmic and nuclear DAF-16::GFP localization, respectively. b) Average proportion of larvae with cytoplasmic, more cytoplasmic, more nuclear, and nuclear DAF-16::GFP localization in intestinal cells after 6 h of L1 starvation. Four biological replicates were performed. At least 50 larvae were scored per genotype per replicate. Error bars represent standard deviations. c) Cochran-Mantel-Haenszel chi-squared tests were conducted for each pair of comparisons between genotypes. ***P < 0.001; n.s. not significant.  alleles. b,d) Body length after 48-h recovery on food was measured using the program WormSizer for image analysis (Moore et al. 2013) for starved (4-day L1 starvation) and control (no starvation) conditions. Body lengths of both males and hermaphrodites were recorded, and no significant difference was found between them, but only the results from hermaphrodites are reported. c,e) Total brood size was scored for each worm in starved (12-h L1 starvation) and control (no starvation) conditions. b-e) Three biological replicates were performed. Mating efficiency was carefully checked by recording numbers of males and hermaphrodites in the images used for WormSizer and only replicates with a 1:1 male to hermaphrodite ratio were included (brood size was determined from the same worm populations). A linear mixed effects (lme) model was fit to the data with the response variable being body length or brood size, fixed effects being the interaction between starvation and genotype, and the random effect being replicates. P-values for interaction terms are reported. Horizontal bars represent estimates calculated by lme models. D values are differences between estimates in starved and control conditions. Each dot represents an observation with a single worm. d, e) ***P < 0.001; n.s. not significant. phosphatase activity (Myers et al. 1998;Rodr ıguez-Escudero et al. 2011), it also lacks some protein-phosphatase activity (Furnari et al. 1998;Myers et al. 1998;Ramaswamy et al. 1999). The crystal structure of PTEN reveals a sole active site pocket that presumably has catalytic activity toward PIP3 and phosphoproteins (Lee et al. 1999), consistent with each mutation affecting both activities. Moreover, although DAF-18 and PTEN share the same PTP signature motif in the catalytic core, they have less homology in the WPD loop (88-98 in PTEN) and TI loop (160-171 in PTEN) that together with the P loop constitute the sidewalls of the active site pocket (Ogg and Ruvkun 1998;Lee et al. 1999;Mihaylova et al. 1999). Therefore, we believe extrapolation from the properties of these PTEN alleles to the homologous daf-18 alleles should be made very cautiously.
In contrast to the other phenotypes assayed, daf-18(D137A) had significantly less effect on M-cell divisions during L1 starvation than the other alleles examined. Likewise, a high-copy daf-18(D137A) transgene functioned like wild-type daf-18 when used to rescue Q-cell quiescence during L1 starvation in the null daf-18(ok480) background (Zheng et al. 2018b). In contrast, daf-18(C169S) and daf-18(G174E) transgenes did not rescue quiescence. These results suggest that the effects of D137A and G174E on DAF-18 function do not completely overlap, as if there is a degree of specificity that can distinguish them in some phenotypic assays (consistent with biochemical characterization of their mammalian homologs; see above). The fact that daf-18(D137A) has less of a relative effect on M or Q-cell divisions than starvation resistance, DAF-16::GFP localization, or dauer development could reflect a difference in the relative sensitivity of the underlying biological process to the lipid and/or protein-phosphatase activities of DAF-18. However, our work together with that of Wittes and Greenwald (submitted in parallel) cautions against using missense alleles (D137A and G174E in particular) in an effort to causally connect specific DAF-18 enzymatic activities with specific phenotypes.

Data availability
Data generated during the process of this study are available in this article. Strains are available upon request. Code for performing statistical tests with starvation survival data is available at https://github.com/jc271828/Chen2022 [accessed 2022 Apr 25].