Abstract
Drosophila melanogaster females eclose on average 4 h faster than males owing to sexual differences in the pupal period, referred to as the protogyny phenotype. Here, to elucidate the mechanism underlying the protogyny phenotype, we used our newly developed Drosophila Individual Activity Monitoring and Detecting System (DIAMonDS) that detects the precise timing of both pupariation and eclosion in individual flies. Although sex transformation induced by tra-2, tra alteration, or msl-2 knockdown-mediated disruption of dosage compensation showed no effect on the protogyny phenotype, stage-specific whole-body knockdown and mutation of the Drosophila master sex switch gene, Sxl, was found to disrupt the protogyny phenotype. Thus, Sxl establishes the protogyny phenotype through a noncanonical pathway in D. melanogaster.
Similar content being viewed by others
Introduction
The time taken to reach sexual maturity is often unequal between the sexes of numerous animal species. Protogyny refers to the phenotype characterized by females maturing first, whereas protandry refers to the phenotype characterized by males maturing earlier than females1,2. Information within the AnAge database (https://genomics.senescence.info/species/) reveals that approximately one-third of the animals across the animal kingdom show sexual dimorphism in the sexual maturation timing, with poikilotherms and homeotherms tending to exhibit protandry and protogyny, respectively (Supplementary Table S1)3. In insects, the terms protandry and protogyny refer to male- and female-specific differences, respectively, in the timing of adult emergence4. Although the AnAge database includes minimal data on arthropods, several reports have indicated that male adults tend to emerge earlier than females in many insect species2,5,6,7,8. Several hypotheses have been proposed to explain the occurrence of protogyny and protandry with respect to increasing fitness. There are some evolutional explanations for sexual maturation based on direct and indirect effects. Some studies have suggested that biased sexual maturation is generally a by-product of sexual size dimorphism (SSD)2,7. On the other hand, some reports suggested that the difference in sexual maturation timing of both sexes has fitness consequences and that selection directly maintains biased sexual maturation phenotype2,8,9. However, the detailed mechanism and a convincing generalized evolutional explanation for the biased sexual maturation trait remain to be provided1,4,7,8,10,11.
To understand the evolutionary significance of the sex bias in the sexual maturation time point, it is also important to elucidate the molecular mechanism underlying the protogyny and protandry phenotypes. However, these molecular aspects remain unclear, mainly owing to difficulties in precisely measuring the timing of maturation of individuals simultaneously and for a long period with the currently available techniques.
In the fruit fly (Drosophila melanogaster), adult females emerge quickly, before males (protogyny phenotype), with only a 4-h difference in eclosion timing12. Therefore, D. melanogaster offers a potentially useful model to elucidate the molecular mechanism underlying the sexual dimorphism in sexual maturation. We established a new system, Drosophila Individual Activity Monitoring and Detection System (DIAMonDS), which can automatically detect the phase-conversion timing of individual flies, such as the timing of pupariation, adult eclosion, and death, with high temporal resolution13. DIAMonDS enables time-lapse- and multi-scanning to simultaneously determine the time points of pupariation and eclosion of individuals under several chemical and environmental conditions and against different genetic backgrounds. As DIAMonDS acquires time-lapse images using a basic flatbed charge-coupled device (CCD) scanner, flies continue to catch the light signal intermittently throughout the day during the time-lapse scanning by DIAMonDS. Therefore, DIAMonDS eliminates the influence of the light-dark cycle on eclosion. Using DIAMonDS, we can precisely detect the 4-h sex-specific difference in eclosion timing, which was found to be solely due to a difference in pupal duration13. Because previous reports also corroborate this result, the 4-h difference in adult emergence between sex seems to reflect intrinsic developmental time to eclosion without the effect of light conditions12.
In D. melanogaster, the sex is determined by the master switch Sex lethal (Sxl) gene, which encodes an RNA splicing enzyme, by modulating the ratio of sex chromosomes to autosomes (X:A)14,15. In females, Sxl activates the transformer (tra) gene by correct splicing, while functional Tra regulates the splicing of the doublesex (dsx) gene with transformer 2 (Tra-2) as a cofactor to produce DsxF, the female-specific Dsx. In contrast, males have no functional Tra protein and express male-specific DsxM. Hence, these DsxF and DsxM proteins induce sex-specific phenotypic changes16,17,18, and the presence or absence of Tra or Tra-2 plays a critical role in determining sexual differentiation. Sex chromosome dosage compensation is differentially regulated by sex, and the male-specific lethal (MSL) complex is a key player in the dosage compensation machinery in Drosophila19,20. In females, dosage compensation is blocked by Sxl-dependent repression of msl-2, which encodes a limiting subunit of the MSL complex21. Although several studies indicate that the genes involved in the sex determinant pathway play a significant role in the expression of the sexual dimorphic traits, its contribution per se for determining the protogyny phenotype has not been reported to date22,23.
In this study, we applied DIAMonDS to evaluate the genetic regulation of the protogyny phenotype in D. melanogaster. As fruit flies alter their developmental rates when exposed to different environmental conditions24,25,26, we first explored the effect of temperature and nutrients on the protogyny phenotype. Next, we manipulated tra and tra-2 to change the sex of the flies and evaluated the effect on the protogyny phenotype. Since sex chromosome dosage compensation is differentially regulated by sex, and the male-specific lethal complex plays a key role in the dosage compensation machinery in Drosophila19,20, we also investigated the possibility that the dosage compensation pathway contributes to the protogyny phenotype by knocking down the expression of msl-2. Finally, we evaluated the potential role of Sxl27,28,29.
Results
Environmental robustness of the protogyny phenotype in D. melanogaster
In D. melanogaster, several environmental conditions, such as temperature and nutritional conditions, influence the duration and rate of development30,31,32,33. Therefore, we first analyzed the environmental robustness of the protogyny phenotype in these flies. We defined the pupal duration as the duration from pupariation to eclosion and measured their timing points using our newly developed DIAMonDS tool (see “Materials and methods”)13. To highlight the sex-specific differences in this study, we focused on the relative pupal duration between females and males. We observed that the sex-specific difference in pupal duration was maintained at a high temperature of 29 °C (Fig. 1A, Supplementary Fig. S1A,B) as well as under varying nutritional conditions, including various concentrations of sucrose and yeast (Fig. 1B,C, Supplementary Fig. S1C,D). These results indicated that the phenotypic stability of the protogyny in D. melanogaster remains robust under environmental perturbation. Therefore, we next evaluated the molecular and genetic aspects underlying protogyny.
Sex transformation does not affect the protogyny phenotype based on the genotype
A previous study revealed that tra-2 knockdown or tra overexpression in the whole body induces a sex transformation so that the phenotypic sex was opposite to the genotypic sex, which also altered body size (Fig. 2A)22. We confirmed that the phenotypic sex transformation of D. melanogaster can be controlled by genetic manipulation of tra or tra-2 expression independent of the sexual genotype using UAS-tra2 RNA interference (RNAi)-mediated knockdown or UAS-traF overexpression with ubiquitous GAL4 drivers (Supplementary Fig. S3A). Pupal durations were then compared between siblings with XX and XY genotypes, respectively (Supplementary Fig. S2). The phenotypic transformation induced by tra-2 knockdown or traF overexpression did not alter the sexual difference of pupal duration based on the chromosomal sex (Fig. 2B,C, Supplementary Fig. S3B–F). These results suggested that phenotypic sex is not critical to the protogyny phenotype, which is also independent of the tra/tra-2 pathway.
Disturbance of the dosage compensation pathway does not alter the protogyny phenotype
The dosage compensation machinery is not assembled in Drosophila females, because msl-2, a key gene involved in the assembly of the MSL complex, is repressed by Sxl (Fig. 3A)19,20,21,34. Thus, we next investigated the possible contribution of the dosage compensation pathway to the development of the protogyny phenotype. Ubiquitous knockdown of msl-2 (Fig. 3A) successfully induced male-specific semi-lethality (Supplementary Fig. S4A), which in turn reduced the msl-2 expression in males (Supplementary Fig. S4B). However, msl-2 knockdown did not change the sexual difference of pupal duration, suggesting that the sex chromosome dosage compensation machinery does not commit to the protogyny phenotype (Fig. 3B,C, Supplementary Fig. S4C–F).
Protogyny phenotype is determined in a Sxl-dependent manner
Although the protogyny is apparently sex-dependent, alteration of the expression of the canonical downstream components of Sxl did not affect the protogyny phenotype. Therefore, we next tested whether Sxl contributed to the protogyny phenotype.
We used trans-heterozygous SxlM1,Δ33/Sxlf7,M1 masculinized females35,36,37 and, through a crossing scheme, produced two genotypes of SxlM1,Δ33/Sxlf7,M1 (Sxl–) flies with and without an extra Sxl transgene (Fig. 4A, Supplementary Fig. S5A). We found that Sxl– females without an extra Sxl transgene experienced a significantly longer pupal duration than did Sxl+ females, which was reversed following introduction of an extra Sxl transgene, suggesting that Sxl may play a role in controlling sex-specific pupal duration (Fig. 4A, Supplementary Fig. S5A). The Sxl– females without an extra Sxl transgene also exhibited a slight but significantly longer pupal duration than SxlM1,Δ33/Y males with or without an extra Sxl transgene. Since the SxlM1,Δ33/Sxlf7,M1 masculinized females have low viability (Supplementary Fig. S5B)35, it is possible that another mechanism regulates the longer pupal duration and delayed eclosion through the adverse effects of Sxl mutation in females.
To exclude the influence of Sxl mutation-induced adverse effects on the pupal duration, we performed RNAi-mediated Sxl knockdown experiments (Fig. 4B, Supplementary Fig. S5E). Since Sxl knockdown using act5c-GAL4 was not successful owing to its lethal phenotype, we used a gene-switch system that induces GAL4 by administration of the glucocorticoid receptor antagonist RU48638. F1 larvae were derived from parents of a UAS-Sxl RNAi transgenic fly and an act5c-GS-GAL4 fly reared in normal conditions, and early 3rd-instar larvae were transferred to a 96-well-microplate containing media with or without RU486. Adult F1 females eclosed from the RU486-supplemented media showed partial morphological sexual transformation, indicating that RU486-dependent Sxl knockdown was successful (Supplementary Fig. S6). The proportion of females was partially recovered by the stage-specific Sxl knockdown in comparison with that of the SxlM1,Δ33/Sxlf7,M1 masculinized females (Supplementary Fig. S5B,F). As a control, we used act5c-GS-GAL4/ + fly and these flies did not show any change in the protogyny phenotype under the condition with/without RU486 (Supplementary Fig. S5C,D). act5c-GS > Sxl RNAi F1 females reared in RU486-supplemented media showed longer pupal duration than the unsupplemented F1 females, and the pupal duration was similar to that of males (Supplementary Fig. S5E). Altogether, these results suggest that Sxl might be involved in the development of the protogyny phenotype.
Discussion
In this study, we applied our recently developed DIAMonDS tool to explore the molecular mechanisms responsible for the slight but consistent sex difference in eclosion timing in Drosophila due to a difference in pupal duration.
Many morphological and physiological traits exhibit a sex difference, which may be controlled by a canonical sex-determination pathway39. However, the protogyny phenotype is not disturbed in genetically sex-transformed flies, established by controlling tra or tra-2 expression, or by knockdown of msl-2. These results suggest that a morphological or physiological (dosage compensation) sex difference does not play a central role in controlling the protogyny phenotype, as manipulating these factors did not influence the length of male pupal duration. However, further genetic manipulation experiments demonstrated that the noncanonical function of Sxl regulates the eclosion timing and produces the protogyny phenotype in D. melanogaster, as females with loss-of-function mutations or knockdown of Sxl exhibited a pupal period of the same length as that of males (Supplementary Fig. S7).
Sxl expression is activated in the presence of two X chromosomes in female early embryos and is maintained via positive autoregulation27,35,40. Sxl also regulates splicing of its downstream components, including tra and msl-2, which play crucial roles in the sex-determination cascade and dosage compensation, respectively15,41. Therefore, our results suggest that the recently identified noncanonical Sxl pathways may be involved in the protogyny phenotype.
Indeed, Sxl has been suggested to interact with other targets. Nanos RNA can bind directly to Sxl in ovarian extracts, and loss-of-function studies suggested that Sxl enables the switch from germline stem cells to committed daughter cells through Nanos posttranscriptional downregulation42. Sxl can also bind to Notch to negatively control the Notch pathway43. Genome-wide computational screening for Sxl targets also identified an ATP-dependent RNA helicase, Rm62, as a novel potential target44. Rm62 was inferred to be involved in alternative splicing regulation and is required for the RNAi machinery45,46. A pan-neuronal RNA-binding protein of the ELAV family, found in neurons, was also shown to be downregulated by Sxl in female heads, independent of tra/tra-2 regulation47. Sxl can enhance nuclear entry of the full-length Cunitus interuptus protein, suggesting a contribution to the sex difference in growth rate, although their physical interaction has not been confirmed48. However, there is no evidence that these noncanonical targets of Sxl directly affect eclosion timing. Therefore, further studies are required to demonstrate whether these Sxl targets, or another novel target, can contribute to the protogyny phenotype. In our study, Sxl mutation and whole-body Sxl knockdown led to delayed eclosion in females. Because loss of Sxl affects female viability, It is very difficult to completely eliminate the possibility that female sickness might induce delayed eclosion. To overcome this problem, further analysis using a novel downstream gene of Sxl would be necessary.
The independence of the protogyny phenotype from the canonical sex-determination pathway is very intriguing with respect to understanding the evolution of the sex difference in sexual maturation. Sxl does not appear to play a role in the sex determination process in most insects37,49,50,51. Several reports indicated that orthologs of Sxl have no sex-determinant role in non-Drosophila species, including in Diptera50,52,53. In Drosophilidae, ancestral Sxl was duplicated to Sxl and sister of sex lethal (ssx); the new ssx plays a role of ancestral Sxl, suggesting that Sxl may have evolved to function as a novel sex-determinant gene in Drosophilidae51. Moreover, a detailed phylogenetic study revealed that a male-specific exon, and likely embryo-specific exon, originated after the divergence between the Drosophilidae and Tephritidae families, but before the split of the Drosophila and Scaptodrosophila genera54. We hypothesize that the implementation of Sxl in the sex-determination pathway may be significantly involved in the acquisition of the protogyny phenotype in Drosophila. Therefore, we expect that identification of the target of the noncanonical Sxl sex-specific regulation for the protogyny phenotype may help to promote a better understanding of the evolutionary aspects of protogyny.
Methods
Drosophila stocks
All flies were maintained at 25 °C on standard laboratory medium as described previously55. The following stocks were obtained from the Bloomington Drosophila stock center (BDSC): w1118 (wild-type; BDSC 5905), act5c-GAL4 (BDSC 3954), da-GAL4 (BDSC8641), elav-GAL4 (BDSC 458), elav-GAL4; UAS-dcr-2 (BDSC 25750), P{CaryP} attP2 (BDSC 36303), UAS-tra2 RNAi #1 (BDSC 56912), UAS-tra2 RNAi #2 (BDSC 28018), UAS-traF (BDSC 4590), UAS-msl-2 RNAi #1 (BDSC 31627), UAS-msl-2 RNAi #2 (BDSC 35390), UAS-Sxl RNAi #1 (BDSC 34393), UAS-Sxl RNAi #2 (BDSC 38195), Sxlf7,M1; P{Sxl. + tCa}9A/ + (BDSC 58486), and SxlM1,fΔ33/Binsinscy (BDSC 58487). Three gene-switch Gal4 driver lines—act5c-GS-GAL4, S106-GS-GAL4, and 5961-GS-GAL4—were kindly gifted by Dr. Akagi56.
Measurement of pupal duration
We used our recently developed DIAMonDS tool to measure pupal duration at the individual level. The wandering 3rd-instar larvae were collected from rearing vials, and a single larva was placed in the well of a 96-well microplate with standard medium. The plate was then placed on a flatbed CCD scanner to obtain time-lapse images until all flies were eclosed. The time-lapse image dataset was then analyzed using Sapphire software as described previously13.
To compare the effect of Sxl mutation on pupal duration, Sxlf7,M1; P{Sxl. + tCa}9A/ + females were crossed with w1118/Y males. The F1 progeny Sxlf7,M1/Y; P{Sxl. + tCa}9A/ + males were then crossed with SxlM1,fΔ33/Binsinscy females. Each genotype of the F2 flies was then assessed for pupal duration using DIAMonDS. To induce the gene-switch Gal4 driver, RU486 (Mifepristone; Sigma, St. Louis, MO, USA) reagent was dissolved in ethanol and added to the medium at a final concentration of 100 µg/mL.
To detect the sex genotype of the flies, genomic DNA was extracted from single adults by homogenization in 50 μL of squishing buffer (10 mM Tris–HCl [pH 8.2], 1 mM EDTA, 25 mM NaCl, and 200 μg/mL proteinase K) and incubated at room temperature for 20 min, followed by inactivation at 95 °C for 5 min. The extracted genomic DNA was subjected to polymerase chain reaction analysis using a WD repeat-containing protein on the Y chromosome (WDY)- and Rp49-specific primer mix by ampliTaq Gold 360 master mix (Applied Biosystems, Waltham, MA, USA), following which the amplified DNA fragments were separated by 2% agarose gel electrophoresis (Supplementary Fig. S1).
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
Total RNA was extracted from the whole adult body (for measuring msl-2 expression knocked down by act5c-GAL4) and dissected larval central nervous system (for measuring Sxl expression knocked down by elav-GAL4) using Isogen II (Nippon Gene, Tokyo, Japan). RT-qPCR was performed using a One Step SYBR PrimeScript PLUS RT-PCR kit (Takara Bio, Shiga, Japan) and Applied Biosystems ABI Prism 7000 Sequence Detection System. All mRNA levels were normalized to those of rp49. We used the following primers for RT-qPCR (5′–3′): Sxl, forward primer (5ʹ-CCAATCTGCCGCGTACCATA-3ʹ), reverse primer (5ʹ-AATGGAACCGTACTTGCCGA-3ʹ); msl-2, forward primer (5ʹ-CACTGCGGTCACACTGGCTTCGCTCAG-3ʹ), reverse primer (5ʹ-CTCCTGGGCTAGTTACCTGCAATTCCTC-3ʹ); and rp49, forward primer (5ʹ-GATGACCATCCGCCCAGCATAC-3ʹ), reverse primer (5ʹ-AGTAAACGCGGTTCTGCATGAGC-3ʹ).
Statistical analysis
All data were analyzed and graphs were plotted using Prism 8 (GraphPad Software, San Diego, CA, USA). Data are presented as the mean ± standard deviation. Student’s unpaired two-tailed t-test was performed to compare differences between two groups in each experiment, and Dunnett’s one-way analysis of variance was used for multiple comparisons; p < 0.05 was considered to indicate a statistically significant difference.
Abbreviations
- CCD:
-
Charge-coupled device
- BDSC:
-
Bloomington Drosophila stock center
- dsx:
-
Doublesex
- DIAMonDS:
-
Drosophila Individual Activity Monitoring and Detection System
- msl-2 :
-
Male-specific lethal-2
- RT-qPCR:
-
Reverse transcription-quantitative polymerase chain reaction
- RNAi:
-
RNA interference
- Sxl :
-
Sex lethal
- ssx :
-
Sister of sex lethal
- tra :
-
Transformer
- WDY :
-
WD repeat-containing protein on the Y chromosome
References
Thornhill, R. & Alcock, J. The Evolution of Insect Mating Systems. ix (Harvard Univ. Pr., 1983).
Morbey, Y. E. & Ydenberg, R. C. Protandrous arrival timing to breeding areas: A review. Ecol. Lett. 4, 663–673. https://doi.org/10.1046/j.1461-0248.2001.00265.x (2001).
de Magalhães, J. P. & Costa, J. A database of vertebrate longevity records and their relation to other life-history traits. J. Evol. Biol. 22, 1770–1774. https://doi.org/10.1111/j.1420-9101.2009.01783.x (2009).
Blanckenhorn, W. U. et al. Proximate causes of Rensch’s rule: Does sexual size dimorphism in arthropods result from sex differences in development time?. Am. Nat. 169, 245–257. https://doi.org/10.1086/510597 (2007).
Thornhill, R. & Alcock, J. The Evolution of Insect Mating Systems (Harvard Univ. Pr., 2014).
Rhainds, M. Female mating failures in insects. Entomol. Exp. Appl. 136, 211–226. https://doi.org/10.1111/j.1570-7458.2010.01032.x (2010).
Teder, T., Kaasik, A., Taits, K. & Tammaru, T. Why do males emerge before females? Sexual size dimorphism drives sexual bimaturism in insects. Biol. Rev. Camb. Philos. Soc. 96, 2461–2475. https://doi.org/10.1111/brv.12762 (2021).
Wiklund, C. & Fagerström, T. Why do males emerge before females? A hypothesis to explain the incidence of protandry in butterflies. Oecologia 31, 153–158. https://doi.org/10.1007/BF00346917 (1977).
Iwasa, Y., Odendaal, F. J., Murphy, D. D., Ehrlich, P. R. & Launer, A. E. Emergence patterns in male butterflies—A hypothesis and a test. Theor. Popul. Biol. 23, 363–379. https://doi.org/10.1016/0040-5809(83)90024-2 (1983).
Degen, T., Hovestadt, T., Mitesser, O. & Hölker, F. High female survival promotes evolution of protogyny and sexual conflict. PLoS One 10, e0118354. https://doi.org/10.1371/journal.pone.0118354 (2015).
Rhainds, M. Ecology of female mating failure/lifelong virginity: A review of causal mechanisms in insects and arachnids. Entomol. Exp. Appl. 167, 73–84. https://doi.org/10.1111/eea.12759 (2019).
Bainbridge, S. P. & Bownes, M. Staging the metamorphosis of Drosophila melanogaster. J. Embryol. Exp. Morphol. 66, 57–80. https://doi.org/10.1242/dev.66.1.57 (1981).
Seong, K. H., Matsumura, T., Shimada-Niwa, Y., Niwa, R. & Kang, S. The Drosophila individual activity monitoring and detection system (DIAMonDS). Elife https://doi.org/10.7554/eLife.58630 (2020).
Bridges, C. B. Triploid intersexes in Drosophila melanogaster. Science 54, 252–254. https://doi.org/10.1126/science.54.1394.252 (1921).
Salz, H. K. & Erickson, J. W. Sex determination in Drosophila: The view from the top. Fly (Austin) 4, 60–70. https://doi.org/10.4161/fly.4.1.11277 (2010).
Inoue, K., Hoshijima, K., Sakamoto, H. & Shimura, Y. Binding of the Drosophila sex-lethal gene product to the alternative splice site of transformer primary transcript. Nature 344, 461–463. https://doi.org/10.1038/344461a0 (1990).
Sosnowski, B. A., Belote, J. M. & McKeown, M. Sex-specific alternative splicing of RNA from the transformer gene results from sequence-dependent splice site blockage. Cell 58, 449–459. https://doi.org/10.1016/0092-8674(89)90426-1 (1989).
Boggs, R. T., Gregor, P., Idriss, S., Belote, J. M. & McKeown, M. Regulation of sexual differentiation in D. melanogaster via alternative splicing of RNA from the transformer gene. Cell 50, 739–747. https://doi.org/10.1016/0092-8674(87)90332-1 (1987).
Zhou, S. et al. Male-specific lethal 2, a dosage compensation gene of Drosophila, undergoes sex-specific regulation and encodes a protein with a ring finger and a metallothionein-like cysteine cluster. EMBO J. 14, 2884–2895. https://doi.org/10.1002/j.1460-2075.1995.tb07288.x (1995).
Kelley, R. L. et al. Expression of Msl-2 causes assembly of dosage compensation regulators on the X chromosomes and female lethality in Drosophila. Cell 81, 867–877. https://doi.org/10.1016/0092-8674(95)90007-1 (1995).
Moschall, R., Gaik, M. & Medenbach, J. Promiscuity in post-transcriptional control of gene expression: Drosophila sex-lethal and its regulatory partnerships. FEBS Lett. 591, 1471–1488. https://doi.org/10.1002/1873-3468.12652 (2017).
Rideout, E. J., Narsaiya, M. S. & Grewal, S. S. The sex determination gene transformer regulates male-female differences in Drosophila body size. PLoS Genet. 11, e1005683. https://doi.org/10.1371/journal.pgen.1005683 (2015).
Sawala, A. & Gould, A. P. Sex-lethal in neurons controls female body growth in Drosophila. Fly 12, 133–141. https://doi.org/10.1080/19336934.2018.1502535 (2018).
Musselman, L. P. et al. A high-sugar diet produces obesity and insulin resistance in wild-type drosophila. Dis. Model. Mech. 4, 842–849. https://doi.org/10.1242/dmm.007948 (2011).
Northrop, J. H. The role of yeast in the nutrition of an insect (Drosophila). J. Biol. Chem. 30, 181–187. https://doi.org/10.1016/S0021-9258(18)86728-X (1917).
Schou, M. F. et al. Metabolic and functional characterization of effects of developmental temperature in Drosophila melanogaster. Am. J. Physiol. Regul. Integr. Comp. Physiol. 312, R211–R222. https://doi.org/10.1152/ajpregu.00268.2016 (2017).
Bell, L. R., Horabin, J. I., Schedl, P. & Cline, T. W. Positive autoregulation of sex-lethal by alternative splicing maintains the female determined state in Drosophila. Cell 65, 229–239. https://doi.org/10.1016/0092-8674(91)90157-t (1991).
Schütt, C. & Nöthiger, R. Structure, function and evolution of sex-determining systems in Dipteran insects. Development 127, 667–677. https://doi.org/10.1242/dev.127.4.667 (2000).
Salz, H. K. Sex determination in insects: A binary decision based on alternative splicing. Curr. Opin. Genet. Dev. 21, 395–400. https://doi.org/10.1016/j.gde.2011.03.001 (2011).
French, V., Feast, M. & Partridge, L. Body size and cell size in Drosophila: The developmental response to temperature. J. Insect Physiol. 44, 1081–1089. https://doi.org/10.1016/s0022-1910(98)00061-4 (1998).
Trotta, V. et al. Thermal plasticity in Drosophila melanogaster: A comparison of geographic populations. BMC Evol. Biol. 6, 67. https://doi.org/10.1186/1471-2148-6-67 (2006).
Economos, A. C. & Lints, F. A. Growth rate and life span in Drosophila. I. Methods and mechanisms of variation of growth rate. Mech. Ageing Dev. 27, 1–13. https://doi.org/10.1016/0047-6374(84)90078-2 (1984).
Ashburner, M. & Thompson, J. (eds.). Laboratory Culture of Drosophila 1978.
Bashaw, G. J. & Baker, B. S. The regulation of the Drosophila msl-2 gene reveals a function for Sex-lethal in translational control. Cell 89, 789–798. https://doi.org/10.1016/s0092-8674(00)80262-7 (1997).
Cline, T. W. Autoregulatory functioning of a Drosophila gene-product that establishes and maintains the sexually determined state. Genetics 107, 231–277. https://doi.org/10.1093/genetics/107.2.231 (1984).
Sawala, A. & Gould, A. P. The sex of specific neurons controls female body growth in Drosophila. PLoS Biol. 15, e2002252. https://doi.org/10.1371/journal.pbio.2002252 (2017).
Evans, D. S. & Cline, T. W. Drosophila switch gene Sex-lethal can bypass its switch-gene target transformer to regulate aspects of female behavior. Proc. Natl. Acad. Sci. U. S. A. 110, E4474–E4481. https://doi.org/10.1073/pnas.1319063110 (2013).
Roman, G., Endo, K., Zong, L. & Davis, R. L. P[Switch], a system for spatial and temporal control of gene expression in Drosophila melanogaster. Proc. Natl. Acad. Sci. U. S. A. 98, 12602–12607. https://doi.org/10.1073/pnas.221303998 (2001).
Millington, J. W. & Rideout, E. J. Sex differences in Drosophila development and physiology. Curr. Opin. Physiol. 6, 46–56. https://doi.org/10.1016/j.cophys.2018.04.002 (2018).
Erickson, J. W. & Quintero, J. J. Indirect effects of ploidy suggest X chromosome dose, not the X: A ratio, signals sex in Drosophila. PLoS Biol. 5, e332. https://doi.org/10.1371/journal.pbio.0050332 (2007).
Bashaw, G. J. & Baker, B. S. Dosage compensation and chromatin structure in Drosophila. Curr. Opin. Genet. Dev. 6, 496–501. https://doi.org/10.1016/s0959-437x(96)80073-6 (1996).
Chau, J., Kulnane, L. S. & Salz, H. K. Sex-lethal enables germline stem cell differentiation by down-regulating Nanos protein levels during Drosophila oogenesis. Proc. Natl. Acad. Sci. U. S. A. 109, 9465–9470. https://doi.org/10.1073/pnas.1120473109 (2012).
Penn, J. K. M. & Schedl, P. The master switch gene Sex-lethal promotes female development by negatively regulating the n-signaling pathway. Dev. Cell 12, 275–286. https://doi.org/10.1016/j.devcel.2007.01.009 (2007).
Robida, M. D., Rahn, A. & Singh, R. Genome-wide identification of alternatively spliced mRNA targets of specific RNA-binding proteins. PLoS ONE 2, e520. https://doi.org/10.1371/journal.pone.0000520 (2007).
Park, J. W., Parisky, K., Celotto, A. M., Reenan, R. A. & Graveley, B. R. Identification of alternative splicing regulators by RNA interference in Drosophila. Proc. Natl. Acad. Sci. U. S. A. 101, 15974–15979. https://doi.org/10.1073/pnas.0407004101 (2004).
Ishizuka, A., Siomi, M. C. & Siomi, H. A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins. Genes Dev. 16, 2497–2508. https://doi.org/10.1101/gad.1022002 (2002).
Sun, X. et al. Sxl-dependent, tra/tra2-independent alternative splicing of the Drosophila melanogaster X-linked gene found in neurons. Genes Genom. Genet. 5, 2865–2874. https://doi.org/10.1534/g3.115.023721 (2015).
Horabin, J. I. Splitting the hedgehog signal: Sex and patterning in Drosophila. Development 132, 4801–4810. https://doi.org/10.1242/dev.02054 (2005).
Morita, S. et al. Precise staging of beetle horn formation in Trypoxylus dichotomus reveals the pleiotropic roles of doublesex depending on the spatiotemporal developmental contexts. PLoS Genet. 15, e1008063. https://doi.org/10.1371/journal.pgen.1008063 (2019).
Meise, M. et al. Sex-lethal, the master sex-determining gene in Drosophila, is not sex-specifically regulated in Musca domestica. Development 125, 1487–1494. https://doi.org/10.1242/dev.125.8.1487 (1998).
Traut, W., Niimi, T., Ikeo, K. & Sahara, K. Phylogeny of the sex-determining gene Sex-lethal in insects. Genome 49, 254–262. https://doi.org/10.1139/G05-107 (2006).
Saccone, G. et al. The Ceratitis capitata homologue of the Drosophila sex-determining gene sex-lethal is structurally conserved, but not sex-specifically regulated. Development 125, 1495–1500. https://doi.org/10.1242/dev.125.8.1495 (1998).
Sievert, V., Kuhn, S., Paululat, A. & Traut, W. Sequence conservation and expression of the sex-lethal homologue in the fly Megaselia scalaris. Genome 43, 382–390. https://doi.org/10.1139/g99-132 (2000).
Zhang, Z., Klein, J. & Nei, M. Evolution of the sex-lethal gene in insects and origin of the sex-determination system in Drosophila. J. Mol. Evol. 78, 50–65. https://doi.org/10.1007/s00239-013-9599-3 (2014).
Seong, K. H. et al. Paternal restraint stress affects offspring metabolism via ATF-2 dependent mechanisms in Drosophila melanogaster germ cells. Commun. Biol. 3, 208. https://doi.org/10.1038/s42003-020-0935-z (2020).
Akagi, K. et al. Dietary restriction improves intestinal cellular fitness to enhance gut barrier function and lifespan in D. melanogaster. PLoS Genet. 14, e1007777. https://doi.org/10.1371/journal.pgen.1007777 (2018).
Acknowledgements
The authors are deeply grateful to Tadashi Uemura (Kyoto University) for the helpful support. They also thank Yuko Iijima and Taishi Matsumura for their technical assistance. We received generous support from Yoichi Shinkai (RIKEN CPR) and Shunsuke Ishii (RIKEN CPR). This work was also supported by the AMED (Japan Agency for Medical Research and Development) [JP18gm1110001 to K.-H.S. and S.K.]. The funding agencies had no role in the collection, analysis, and interpretation of data, in the writing of the report, or in the decision to submit the article for publication.
Author information
Authors and Affiliations
Contributions
Conceptualization, K.-H.S.; methodology, K.-H.S. and S.K.; investigation, K.-H.S. and S.K.; writing—original draft, K.-H.S.; writing—reviewing & editing, K.-H.S. and S.K.; visualization, K.-H.S.; funding acquisition, K.-H.S. and S.K.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Seong, KH., Kang, S. Noncanonical function of the Sex lethal gene controls the protogyny phenotype in Drosophila melanogaster. Sci Rep 12, 1455 (2022). https://doi.org/10.1038/s41598-022-05147-5
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-022-05147-5
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.