In general, the master switch gene for sex determination is expressed for a limited period during the early embryonic stage. To increase our understanding of the sex determination mechanism in Bombyx mori, it is important to understand when sex determination takes place. To examine the key stages for sex determination in this insect, we focused on the expression patterns of Bmdsx (a double-switch gene in the sex determination cascade of B. mori) and BmIMP (a gene expressed specifically in males involved in male-specific splicing of Bmdsx). Reverse transcription PCR (RT-PCR) analysis revealed that male-type Bmdsx expression was observed in females at 27 and 29 h after oviposition (hao), and finally disappeared at 32 hao. Moreover, BmIMP mRNA was also expressed in these females, and its expression level was comparable to that of the male-type Bmdsx mRNA. These results demonstrated that female embryos before 32 hao can show male-type expression of Bmdsx and BmIMP, suggesting that sex determination occurs between 29 and 32 hao, which correspond to the developmental stages from the head lobe differentiation to spoon-shaped embryo stages. This also suggests that the master switch gene for sex determination of B. mori is expressed in females during this period and represses the male-specific mode of expression in sex-determining genes.
Bmdsx, an orthologue of doublesex (dsx), displays sex-specific expression in various tissues in B. mori. The male- and female-specific splice isoforms of Bmdsx encode male-specific BmDSX protein (BmDSXM) and female-specific DSX proteins (BmDSXF), respectively (Suzuki et al. 2001). Ectopic expression of BmDSXM in females resulted in abnormal differentiation of certain female-specific genital organs and caused partial male differentiation in female genitalia (Suzuki et al. 2005). In contrast, BmDSXF functions as a positive regulator of the hexameric storage protein SP1 and vitellogenin genes, which are expressed predominantly in females (Suzuki et al. 2003). Therefore, Bmdsx functions as a double-switch gene at the bottom of the sex determination cascade of B. mori. In Drosophila melanogaster, female-specific splicing of dsx requires TRA, TRA-2, and the exonic splicing enhancer elements located within the dsx fourth exon (Nagoshi and Baker 1990). However, a tra orthologue has not been identified in the Bombyx genome (Mita et al. 2004). Moreover, RNAi knockdown of the Bombyx orthologue of tra-2 has no influence on sex-specific splicing of Bmdsx pre-mRNA (Suzuki et al. 2012). These facts strongly suggest that the mechanism of sex-specific splicing at the doublesex gene differs between D. melanogaster and B. mori. In B. mori, the splicing inhibitor BmPSI and the Bombyx mori insulin-like growth factor II mRNA-binding protein (BmIMP) are involved in the regulation of male-specific splicing of Bmdsx (Suzuki et al. 2010). BmIMP is localized on the Z chromosome and is male-specifically expressed in various tissues. Therefore, BmIMP is thought to play a role in the sex determination cascade in B. mori. Genetic studies have revealed that female sex in B. mori is determined by the presence of a dominant feminizing factor, Feminizer (Fem), on the W chromosome (Tanaka 1916). However, Fem has not yet been identified and its function remains unknown. In general, the master switch gene for sex determination is expressed for a limited period during the early embryonic stage. For example, the expression of Sry, which is the master switch gene for mammalian sex determination, is regulated in a strictly time-dependent manner. Sry is expressed between approximately E10.5 and E12.5, with a peak at E11.5 (Kashimada and Koopman 2010). Sex-lethal (Sxl), which is the master switch gene at the top of the sex determination cascade in Drosophila (Salz et al. 1989), and DM-W, which is a probable sex-determining gene in Xenopus laevis, are both expressed within a narrow time frame (Yoshimoto et al. 2008). Therefore, determining when sex determination occurs may facilitate identification of the master switch gene for sex determination in B. mori.
In the present study, expression patterns of Bmdsx and BmIMP at different embryonic stages were investigated by reverse transcription PCR (RT-PCR) to determine the key stages for sex determination in B. mori. We found that sex determination of B. mori occurs between 29 and 32 hao. In contrast to our expectations, female embryos at 27 and 29 hao expressed male-specific Bmdsx and BmIMP, as well as female-specific Bmdsx. Our results support the concept that the master switch gene for sex determination in B. mori is expressed in females between 29 and 32 hao and represses the male-specific mode of expression in sex-determining genes. To our knowledge, this is the first report of the identification of the sex determination stage in lepidopteran insects.
Materials and methods
We used two silkworm strains; namely, pnd-w1, a non-diaposed and white egg strain maintained in the National Institute of Agrobiological Sciences, and S-1, a non-diaposed and sex-limited black egg strain. For this strain, the pink-eyed white egg (pe/pe) is male (Z/Z) while the black-eyed black egg (+pe/pe) is female (Z/W) and homozygous for pnd. This strain has a large chromosome composed of the W chromosome, chromosome 2 bearing the p B gene, and chromosome 5 bearing the +pe gene (Tanaka et al. 2000). Therefore, eggs of this sex-limited strain, in which females have a genotype of T (W; 2, 5) pB +pe, pe (egg, black; larva, black) and males have a genotype of pe (egg, white; larva, white), were examined. The developing eggs were incubated at 25 °C. Larvae were reared on an artificial diet (Nihon Nosan) at approximately 25 °C.
Male and female moths were mated for 3 h at 25 °C. The female moths were then kept at 5 °C overnight. To collect oviposited eggs, female moths were transferred to the rearing room and allowed to lay eggs every 0.5 h at 25 °C. These eggs were stored at 25 °C.
Microscopic observation of eggs
Eggs were observed using a stereomicroscope (SZX12, Olympus). Microscopic images were photographed using a DP50-CU (Olympus).
RNA extraction and RT-PCR
Total RNA was extracted from each egg using Isogen (Nippon Gene), as described previously (Suzuki et al. 2012). RT-PCR reactions were performed as described previously (Suzuki et al. 2012). The female- and male-specific Bmdsx isoforms were amplified with primers FDSX-F2 (5′-CGC CTT ACC GCA GAC AGG CAG-3′) and FDSX-R4 (5′-GCG CAG TGT CGT CGC TAC AAG G-3′) under the following conditions: 94 °C for 2 min, 35 cycles of 98 °C for 10 s, 57 °C for 30 s, and 72 °C for 1 min, followed by 72 °C for 2 min. BmIMP cDNA was amplified as described previously (Suzuki et al. 2010). Amplification of GAPDH cDNA as a positive control for the RT-PCR reaction was performed using primers GAPDH-F (5′-GCC GCA TTG GCC GTT TGG TGC-3′) and GAPDH-R (5′-CAT GAA CAG TAG TCA TCA AGC-3′) under the following conditions: 94 °C for 2 min, 26 cycles of 98 °C for 10 s, 57 °C for 30 s, and 72 °C for 1 min, followed by 72 °C for 2 min.
Quantitative real-time RT-PCR
Quantitative real-time RT-PCR assays were performed using SYBR Premix Ex Taq II (TaKaRa Bio, Inc.) on a Thermal Cycler Dice Real Time System (TaKaRa Bio, Inc.) according to the manufacturer’s instructions. BmIMPE7-F (5′-ATG CGG GAA GAA GGT TTT ATG-3′) and BmIMP-R (5′-TCA TCC CGC CTC AGA CGA TTG-3′) were used for the quantification of the BmIMP gene expression. GAPDH-F and GAPDH-R were used for the quantification of GAPDH as an internal standard. The threshold cycle (CT) value was normalized with the CT value of the GAPDH gene using Multiplate RQ software (TaKaRa Bio, Inc.).
Results and discussion
To determine the key stages for sex determination, we investigated developmental changes in the expression patterns of Bmdsx and BmIMP by RT-PCR analysis with total RNA extracted from ovarian eggs and eggs at 12, 24, 48, and 120 h after oviposition (hao). Molecular sexing by PCR using W chromosome-specific primers is often used to discriminate female eggs from male eggs. However, our previous study demonstrated that molecular sexing is not applicable to eggs at early developmental stages as more than 30 % have a significant number of polar-body-derived cells (Sakai et al. 2013). For this reason, RT-PCR (Fig. 1) was performed without sexing of the examined eggs. Nine eggs at each stage were subjected to the analysis. Ovarian eggs and eggs at 12 hao expressed the female-specific Bmdsx (BmdsxF) isoform, but did not express BmIMP (Fig. 1b, c). Both BmdsxF and the male-specific Bmdsx isoform (BmdsxM) were expressed in all examined eggs at 24 hao (Fig. 1d). These eggs also expressed BmIMP. In contrast, two types of expression patterns were observed in individuals at 48 hao; some individuals expressed BmdsxF without BmIMP expression, while others expressed both BmdsxM and BmIMP (Fig. 1e). It is possible that the former group was female and the latter group was male. These results suggested that the sex determination occurred between 24 and 48 hao.
To further explore the key stages for sex determination, eggs obtained from a sex-limited strain, S-1, were subjected to the same analysis as described in Fig. 1. Eggs of the sex-limited strain displayed differences in pigmentation according to the sex; nonpigmented (white) eggs were male, while pigmented (black) eggs were female (see “Materials and methods”). We found that several eggs from S-1 strain started to pigment at 27 hao under our experimental conditions (Fig. 2a). A total of 30 eggs with the same extent of incomplete pigmentation as in Fig. 2a were collected at 29 hao and kept at 25 °C. All these eggs completely pigmented before 96 hao (Fig. 2b). This suggested that eggs with incomplete pigmentation at 27–29 hao can be considered genetically ZW females. However, that does not necessarily mean that nonpigmented eggs are all males since most female eggs did not start to pigment during those stages. Some batches at 32 hao (eggs from a single pair mating) contained incompletely pigmented eggs and nonpigmented eggs at a ratio of 1:1 (Fig. 2c), which is equal to the sex ratio in B. mori. Therefore, we regarded these nonpigmented eggs as genetically ZZ males. Based on these findings, female eggs were collected after 27 hao, while male eggs were collected after 32 hao in this study.
The same RT-PCR analysis as described in Fig. 1 was performed using pooled total RNA isolated from either 10 female eggs or 10 male eggs. As shown in Fig. 3a, females at all examined stages highly expressed the BmdsxF isoform. Surprisingly, BmdsxM and BmIMP were markedly expressed in females at 27 and 29 hao. The expression level of the BmdsxM isoform correlated with that of BmIMP. The expression of BmdsxM and BmIMP mRNAs were dramatically diminished in female eggs after 32 hao (Fig. 3a, b). The reduction in the expression level of BmIMP mRNA in female eggs was also confirmed by the RT-qPCR (Fig. 3c). However, males at all examined stages highly expressed BmdsxM and BmIMP. These results demonstrated that female embryos before 32 hao can induce male-specific expression of Bmdsx and BmIMP, suggesting that sex determination occurs between 29 and 32 hao. The embryos at 29 hao and 32 hao are expected to be in the head lobe differentiation stage (stage 5) and spoon-shaped embryo stage (stage 6), respectively (Takami and Kitazawa 1960). Therefore, the sexual fate of B. mori would be determined during the early stages of spoon-shaped embryos.
Our results also suggested that the expression level of BmIMP was comparable to that of BmdsxM (Figs. 1 and 3a). BmIMP physically interacts in vitro with BmPSI, which is expressed in both sexes, and the transfection of cDNAs encoding these two proteins into female cultured cells induces male-specific splicing of Bmdsx (Suzuki et al. 2010). Therefore, it is possible that the expression of BmdsxM in females is mediated by the expression of BmIMP. This supports that BmIMP plays a crucial role in male sex determination. The function of BmIMP in sex determination is currently being explored.
The sexual fate of B. mori is determined genetically; ZW for females and ZZ for males (Tanaka 1916). A putative female-determining gene, Feminizer (Fem), is thought to be located on the W chromosome. However, Fem has not yet been identified and the function of this gene remains unknown. As described above, our results indicate that female embryos in early developmental stages are capable of inducing male-specific expression of Bmdsx and BmIMP. This suggests that the master switch gene for sex determination of B. mori is expressed in females during the early developmental stages (during the early spoon-shaped embryo stage) and represses the male-specific mode of expression in sex-determining genes, including Bmdsx and BmIMP (Fig. 4). We are attempting to identify a W chromosome-specific gene that is expressed exclusively in females during the sex determination stage to identify the dominant female-determining gene, Fem.
Kashimada K, Koopman P (2010) Sry: the master switch in mammalian sex determination. Development 137:3921–3930
Mita K, Kasahara M, Sasaki S, Nagayasu Y, Yamada T, Kanamori H et al (2004) The genome sequence of silkworm, Bombyx mori. DNA Res 11:27–35
Nagoshi RN, Baker BS (1990) Regulation of sex-specific RNA splicing at the Drosophila doublesex gene: cis-acting mutations in exon sequences alter sex-specific RNA splicing patterns. Genes Dev 4:89–97
Sakai H, Yokoyama T, Abe H, Fujii T, Suzuki MG (2013) Appearance of differentiated cells derived from polar body nuclei in the silkworm, Bombyx mori. Front Physiol 4:235
Salz HK, Maine EM, Keyes LN, Samuels ME, Cline TW, Schedl P (1989) The Drosophila female-specific sex-determination gene, Sex-lethal, has stage-, tissue-, and sex-specific RNAs suggesting multiple modes of regulation. Genes Dev 3:708–719
Shukla JN, Jadhav S, Nagaraju J (2011) Novel female-specific splice form of dsx in the silkworm, Bombyx mori. Genetica 139:23–31
Suzuki MG, Ohbayashi F, Mita K, Shimada T (2001) The mechanism of sex-specific splicing at the doublesex gene is different between Drosophila melanogaster and Bombyx mori. Insect Biochem Mol Biol 31:1201–1211
Suzuki MG, Funaguma S, Kanda T, Tamura T, Shimada T (2003) Analysis of the biological functions of a doublesex homologue in Bombyx mori. Dev Genes Evol 213:345–354
Suzuki MG, Funaguma S, Kanda T, Tamura T, Shimada T (2005) Role of the male BmDSX protein in the sexual differentiation of Bombyx mori. Evol Dev 7:58–68
Suzuki MG, Imanishi S, Dohmae N, Asanuma M, Matsumoto S (2010) Identification of a male-specific RNA binding protein that regulates sex-specific splicing of Bmdsx by increasing RNA binding activity of BmPSI. Mol Cell Biol 30:5776–5786
Suzuki MG, Suzuki K, Aoki F, Ajimura M (2012) Effect of RNAi-mediated knockdown of the Bombyx mori transformer-2 gene on the sex-specific splicing of Bmdsx pre-mRNA. Int J Dev Biol 56:693–699
Takami T, Kitazawa T (1960) Normal stages of the embryonic development in the silkworm, Bombyx mori. Tech Bull Sericult Exp Sta 75:1–31 (in Japanese)
Tanaka Y (1916) Genetic studies in the silkworm. J Coll Agric Sapporo 6:1–33
Tanaka N, Yokoyama T, Abe H, Tsuchida K, Ninagi O, Oshiki T (2000) Cytogenetic analysis shows that the unusually large chromosome in the sex-limited p(B) silkworm (Bombyx mori) strain consists of three chromosomes. Hereditas 133:95–103
Yoshimoto S, Okada E, Umemoto H, Tamura K, Uno Y, Nishida-Umehara C, Matsuda Y, Takamatsu N, Shiba T, Ito M (2008) A W-linked DM-domain gene, DM-W, participates in primary ovary development in Xenopus laevis. Proc Natl Acad Sci U S A 105:2469–2474
This work was supported by a Grant-in-Aid for Scientific Research (B), 23380032, 2011.
Communicated by Siegfried Roth
About this article
Cite this article
Sakai, H., Aoki, F. & Suzuki, M.G. Identification of the key stages for sex determination in the silkworm, Bombyx mori . Dev Genes Evol 224, 119–123 (2014). https://doi.org/10.1007/s00427-013-0461-9
- Sex determination
- Bombyx mori
- Insulin-like growth factor II mRNA-binding protein