Open Access
How to translate text using browser tools
1 September 2002 Germ Cell Lineage from a Single Blastomere at 8-Cell Stage in Shiro-uo (ice goby)
Taiju Saito, Satoshi Otani, Terumi Nagai, Takako Nakatsuji, Katsutoshi Arai, Etsuro Yamaha
Author Affiliations +

Shiro-uo (ice goby; teleost fish), Leucopsarion petersii, shows a unique cleavage pattern characterized by two tires of blastomeres at 8-cell stage, like that of echinoderm and amphibian embryo. Such a pattern is suitable to isolation and cell lineage experiments. In this study, cell lineage of germ-line was traced by histological observation and cell labelling experiment at the 8-cell stage. Primordial germ cells (PGCs) were first detected histologically at the 10-somite stage, and migrated to gonadal anlage at 10 days post-fertilization, through usual way described in other teleost species. When a single blastomere was labelled with tracer dye at 8-cell stage, both upper and lower tires generated labelled PGCs at gonadal anlage although upper tires occasionally. This result suggests that all blastomeres at the 8-cell stage have potential to produce PGCs in shiro-uo.


Cell lineage study reveals developmental system about degrees of regulation and mosaicism in embryogenesis of a given species. In general, the more mosaicism of development increases, the more invariable cell lineage is, because the given cytoplasmic factors distribute a fixed blastomere (Davidson, 1990).

In teleost, cell lineage seems to be variable before early gastrulation (Kimmel et al., 1990), suggesting that the development is comparatively more regulative than mosaic in embryogenesis. Actually, extirpation and transplantation treatments of blastoderm before the blastula stage do not affect following development in several species (Fundulus, Oppenhemer, 1936; goldfish, Tung et al., 1944; Yamaha et al., 1997; zebrafish, Lin et al., 1992; medaka, Wakamatsu et al., 1994; rainbow trout, Takeuchi et al., 2001). On the other hand, germ cell lineages in teleost fish are not regulative, because extirpation of lower blastoderm at the blastula stage affects the number of PGCs at gonadal anlage (Kazama-Wakabayashi et al., 1999). Germ cell lineage inherits maternal factors during early cleavage stage in zebrafish, including vasa and nanos mRNA (Yoon et al., 1997; Köprunner et al., 2001). The maternal factors aggregated at marginal parts of early cleavage planes, are inherit to single cells located marginal part of blastoderm at the mid-blastula stage, and thereafter establish germ cell lineage in zebrafish (Yoon et al., 1997; Knaut et al., 2000) and goldfish (Otani et al., 2002). In marginal part of blastoderm, cytoplasm of marginal blastomeres join through yolk cell during early cleavage stage and collapse into yolk cell to form yolk syncytial layer after MBT (Kimmel and Law, 1985; Gevers et al., 1992; Yamaha et al., 1999). Therefore, it is difficult to trace germ cell line by cell labelling with tracer dye.

Shiro-uo (ice goby), Leucopsarion petersii, shows a unique cleavage pattern among fish embryos (Nakatsuji et al., 1997; Arakawa et al., 1999). During the initial steps of embryogenesis, the first two vertical cleavages produce 4 blastomeres on the yolk surface at the 4-cell stage. The third cleavage is horizontal in all blastomeres, and produces two tiers of blastomeres at the 8-cell stage. This cleavage pattern of blastodisc is resemble that of echinoderm and amphibian embryo. Therefore, the blastomeres at the 8-cell stage are suitable for cell lineage study, using tracer dye, because of the complete division of blastomeres without connection at this stage. The mechanical extirpation of upper tiers does not affect following development, suggesting the presence of regulative developmental system in shiro-uo (Saito et al., 2001). Germ cell lineage, however, has not been studied in this species.

In the present study, we first describe the positioning of PGCs during embryonic development by histological observation, and next trace blastomere lineage at 8-cell embryo by cell labelling, in order to elucidate establishment of germ cell lineage.


Animals and gametes

Adult ice goby (shiro-uo), Leucopsarion petersii, used in this study, were purchased from local dealers. Maturation, fertilization, dechorionation and cultivation procedure were according to the method of Saito et al. (2001). Staging of embryo was according to Arakawa et al. (1999).

Injection of tracer dye

In order to reveal cell lineage from upper or lower blastomeres at the 8-cell stage, we used fluorescent dye as a tracer. Injected solution was a 5% Biotin-Dextran-fixable (Sigma) and 5% FITCDextran (Sigma) in 0.2M KCl. The embryos in which the tracer dye leaked from labelled blastomere to adjacent ones by checking under fluorescence microscope were discarded. Blastomeres with Biotin-Dextran-fixable was histologically detectable. Injected embryos were incubated in the culture medium at 19°C according to Saito et al. (2001), and fixed with Bouin's fixative for 2 hr, and used for histological analysis (described below).

Optical analysis

Fluorescence photomicrographs of embryos were taken by using an inverted microscope (Zaiss Axiovert 135) with transmission optics and an automatic camera. FITC fluorescence images were observed by Zaiss filter set.


For histological observation, embryos were fixed with Bouin's fixative for 2 hr, dehydrated in a butyl alcohol series and embedded in paraffin. Serial sections were cut at a thickness of 8 μm, and stained with hematoxylin-eosin, using standard procedures. PGCs were confirmed based on location and characteristics similar to those observed in other teleosts; round shape, relatively large size, large nuclei, and clear nuclear membrane (Hamaguchi, 1982; Timmermans and Taverne, 1989; Braat et al., 1999; Kazama-Wakabayashi et al., 1999; Nagai et al., 2001).

For cell fate analysis, sections of biotin-labelled embryos were attached to slide glasses by 0.005% poly-L-lysine (WAKO). Biotin-labelled cells were stained with diaminobenzidine (DAB) using Histofine SAB-PO (M) kit (Nichirei Co. Ltd.).


Migration of the PGCs in shiro-uo embryo

To identify the localization of the PGCs, we analyzed paraffin sections of shiro-uo embryos from 50%-epiboly (24 hr postfertilization [hpf]) stage until hatch out stage (13 days postfertilization [dpf]) of development. Initially, we observed the morphology of PGCs at 10 dpf, and then traced back the location of PGCs using the characteristics, described above. PGCs were found around the upper part of body cavities, the future gonadal region. Their sizes varied between 10 and 20 μm in major diameter, and PGCs were apparently larger than other surrounding cells. The cytoplasm was stained faintly with eosin.

PGCs were first detectable histologically at the 10-somite stage (50 hpf). Before 10-somite stage embryo, we couldn't distinguish PGCs from somatic cells, because of yolk granules in blastomeres. Yolk granules disturbed histo-logical detection of PGCs. At the 10-somite stage, PGCs were located at mesendodermal region lateral to embryonic body and close contact to the YSL (Fig. 1A, B). At the 20-somite stage, the location of PGCs were shifted medially, and located in mesendodermal region (Fig. 1C, D). At the 30-somite stage, the locations of PGCs were more medially, and some PGCs were in contact with the gut primordium (Fig. 1E, F). At the 5 dpf, PGCs were positioned at the inside of lateral plate mesoderm (Fig. 1G, H). At the 6 dpf, the locations of PGCs were shifted dorsally along inside of lateral plate mesoderm and some PGCs are located at the upper part of gut (Fig. 1I, J). At the 7-9 dpf, when the body cavity was expanded, PGCs were located on the peritoneum dorsal to the intestine (Fig. 1K, L). At the 10 dpf, PGCs were located at the upper part of the body cavity. PGCs were situated at both sides of the upper part of body cavity (Fig. 1M, N). At the 13 dpf, the pair of PGCs clusters were observed at the dorsal part of body cavity. The clustered PGCs were covered with the somatic cells (Fig. 1O-R).

Fig. 1

Distribution of PGCs in transverse sections of shiro-uo embryos. (A-B) 10-somite. (C–D) 20-somite. (E–F) 30-somite. (G–H) 5 dpf. (I–J) 6 dpf (K, L) 8 dpf. (M, N) 10 dpf, (O–R) 13 dpf. B, D, F, H, J, L, N, P, and R, are higher magnification of A, C, E, G, I, K, M, O, and Q., respectively. Arrows and arrowheads indicate PGCs. g, gut; no, notochord; nt, neural tube; sb, swim bladder; y, yolk. Scale bars indicate 50 μm.


The numbers of the PGCs were different in each individual even at the same stage, but the average number of the PGCs was almost conserved in embryos from 10-somite to 10-dpf stages (Table 1).

Table 1

Number of PGCs in embryos at the 10-somite stage and 10 dpf


Clonal analyses by tracer injection into 8-cell blastomere

When the tracer dye was injected into single blastomere, resultant embryos continued to develop, and tracer dye was transmitted only to the clonal progeny of a founder blastomere. The clonal descendants of the blastomere were dispersed among other blastomeres in the blastoderm. The dispersion of labelled cells gradually initiated after 15 hpf, the blastula stage (Fig. 2A, B). During early epiboly (20 hpf), labelled cells were located around almost entire blastoderm. Histological detection of biotin-labelled cells revealed active shape after the 15 hpf. They showed protrusions from their main bodies (Fig. 2C). After 16 hpf, labelled cells had distance each other (Fig. 2D). At 10 dpf, labelled cells were histologically observed at almost all organs. Thus, both upper and lower blastomeres at the 8-cell stage differentiated to various kinds of cells belonging to all the three germ layers.

Fig. 2

FITC-biotin-labelled descendants from upper or lower blastomere of 8-cell stage. (A) Fluorescent view of an upper-blastomere-labelled embryo at the blastula. (B) Fluorescent view of a lower-blastomere-labelled embryo at the blastula. (C, D) Histological detection of descendants of labelled upper-blastomere at 15 hpf and 16 hpf. Arrow indicates cytoplasmic protrusion. (E, F) Histological detection of descendants of labelled blastomere at 10-dpf. Single upper (E) or lower (F) blastomere of 8-cell stage embryo was labelled. Arrows indicate unlabelled (E) and labelled (F) PGCs. Scale bars indicate 50 μm.


When labelled PGCs were counted at the gonadal anlagen of 10 dpf in labelled embryos, labelled PGCs were identified in all embryos developed from labelling of lower blastomere. The number of labelled PGCs varied from 3 to 8 in 10 embryos. In the case of labelling of upper blastomere, only 2 out of 11 resultant embryos had labelled PGCs with 4 or 5 in number (Fig 2E, F. Table 2).

Table 2

Number of biotin-labelled PGCs in 10 dpf embryos after labelling of a single upper or lower blastomere at the 8-cell stage



In shiro-uo, PGCs were first detected at the 10-somite stage. Because yolk granules were distributed in all cells of embryonic body until early segmentation period, like in goldfish (Kazama-Wakabayashi et al., 1999), it was difficult to distinguish PGCs from surrounding somatic cells. In both zebrafish and goldfish, histological detection of PGCs is later in development than those of identification of vasa tran-scripts, germ line maker (Nagai et al., 2001; Otani et al., 2002). Therefore, it must be difficult to identify PGCs by histological characters in teleost at early developmental stage.

In final step of PGCs migration to the gonadal anlage, it is shown that PGCs are related to the inner layer of lateral plate mesoderm in other teleost fish (Richards and Thompson, 1921; Hann, 1927; Jhonston, 1951). But in medaka embryo, when PGCs migrate dorsalward, they are related to the outer layer of lateral plate mesoderm (Gamo, 1961; Hamaguchi, 1982). In the shiro-uo, the present study reveals that PGCs migrated through former route. Finally, the PGCs were covered with somatic cells at 13 dpf, suggesting gonadal formation thereafter.

In shiro-uo, the clonal cells of labelled blastomere, showing pseudopodia, scattered among unlabelled cells at blastula stage, finally differentiated almost all tissues from the three germ layers. The mixing pattern, described here, clearly shows that developmental fate of shiro-uo blastoderm is undetermined at the blastula stage. Namely, blastomeres have pluripotency at this stage. Moreover, our previous report shows that shiro-uo embryos without yolk cell at the 8-cell stage develop abnormally, although without upper tire of blastomeres develop normally (Saito et al., 2001). These results suggest that differentiation of blastoderm is integrated by inductions from yolk cell after blastula stage like shown in zebrafish and goldfish (Mizuno et al., 1996; Mizuno et al., 1997; Mizuno et al., 1999; Yamaha et al., 1998).

Origins of PGCs were investigated by cell linage experiments and indicated that PGCs were mainly originated from lower blastomeres at the 8-cell stage. In zebrafish embryo, molecular marker vasa gene has identified PGCs origins (Yoon et al., 1997; Knaut et al., 2000). Maternal vasa tran-scripts are localized around the blastodisc at the one-cell stage (Braat et al., 1999; Howley and Ho., 2000). At the twoto four-cell stage, vasa transcripts are localized along the first and second cleavage plane, and eventually these clumps localize into four cells at the 32-cell stage (Yoon et al., 1997). The present results are generally consistent with the zebrafish pattern. But PGCs sporadically rose from upper blastomeres at the 8-cell stage in shiro-uo. Recently, vasa gene was isolated in shiro-uo. The expression pattern of vasa by whole mount in situ hybridization reveals that germ cell lineage is detected from early cleavage stage (Miyake et al., 2001). This suggests existence of germ-line determinants from early cleavage stage in shiro-uo. In shirouo, vasa transcripts are observed at the one- and two-cleavage furrows. Moreover, at the 16-cell stage, new four dots of vasa transcripts are frequently observed just under the upper blastomeres, although not confirmed at the 8-cell stage. In the goldfish, vasa gene transcripts are always identified at the third-cleavage furrows, in addition to oneand two- cleavage furrows (Otani et al., 2002). In zebrafish, occasional signals are observed at third-cleavage plane, but are weaker than those at the first and second furrows (Yoon et al., 1997). The frequency of labelled PGCs originated from upper blastomere in 10 dpf embryos is low (2/11 embryos). This possibly suggests that the descendants of lower blastomeres receive the germinal factors include vasa transcripts with high frequency more than upper blastomeres one.

We previously showed pluripotency of blastomere by extirpation experiment in shiro-uo embryo at 8-cell stage (Saito et al., 2001). Moreover, in this study, we revealed that all the blastomeres had a potential to produce the PGCs. This indicates that shiro-uo could be useful model to study PGCs because their blastomeres are suitable for isolation and transplantation experiments at early cleavage stage.


We thank Mr. Shizuo Kimura, Ms. Chikako Nishida, the members of Nanae Fresh Water Laboratory (Field Science Center for Northern Biosphere, Hokkaido University), and the members of Cell Biology Laboratory of Tokai University Center for Advanced Technology (Department of Marine Biology, Graduate School of Marine Science and Technology, Tokai University) for their supports. This study was supported by Grants-in-Aid from the Ministry of Education, Science and Culture of Japan (No. 12460081), Showa Shell Sekiyu Foundation for Promotion of Environmental Research to E Yamaha and the Research Fellowships of the Japan Society for the Promotion of Science for Young Scientists, to T Saito.



T. Arakawa, Y. Kanno, N. Akiyama, T. Kitano, N. Nakatsuji, and T. Nakatsuji . 1999. Stages of embryonic development of the ice goby (shirouo), Leucopsarion petersii. Zool Sci 16:761–773. Google Scholar


A. K. Braat, T. Zandbergen, S. van de Water, H. J. Goos, and D. Zivkovic . 1999. Characterization of zebrafish primordial germ cells: morphology and early distribution of vasa RNA. Dev Dyn 216:153–167. Google Scholar


E. H. Davidson 1990. How embryos work: a comparative view of diverse modes of cell fate specification. Development 108:365–389. Google Scholar


Gamo 1961. On the origin of germ cells and formation of gonad primordia in the medaka, Oryzias latipes. Jpn J Zool 13:101–115. Google Scholar


P. Gervers, J. Duros, J. G. M. Van Den Boogaat, and L. P. M. Timmermans . 1992. A study on cell lineage, especially the germ cell line, in embryos of the teleost fish, Barbus conchonius. Roux's Arch Dev Biol 201:275–283. Google Scholar


S. Hamaguchi 1982. A light- and electron-microscopic study on the migration of primordial germ cells in the teleost, Oryzias latipes. Cell Tissue Res 227:139–151. Google Scholar


H. W. Hann 1927. The history of the germ cells of Cottus bairdii Girard. J Morphol Physiol 43:427–497. Google Scholar


Johnston 1951. The embryonic histology of the germ cells of the largemouth black bass, Micropterus salmoides salmoides (Lacépède). J Morphol 88:471–542. Google Scholar


C. Howley and R. K. Ho . 2000. mRNA localization patterns in zebrafish oocytes. Mech Dev 92:305–309. Google Scholar


M. Kazama-Wakabayashi, E. Yamaha, and F. Yamazaki . 1999. The elimination and duplication of lower part of blastoderm effects on the number of primordial germ cells in goldfish. Fisheries Sci 65:577–582. Google Scholar


C. B. Kimmel and R. D. Law . 1985. Cell lineage of zebrafish blastomeres. I. Cleavage pattern and cytoplasmic bridges between cells. Dev Biol 108:78–85. Google Scholar


C. B. Kimmel, R. M. Warga, and T. F. Schilling . 1990. Origin and organization of the zebrafish fate map. Development 108:581–594. Google Scholar


H. Knaut, F. Pelegri, K. Bohmann, H. Schwarz, and C. Nusslein-Volhard . 2000. Zebrafish vasa RNA but not its protein is a component of the germ plasm and segregates asymmetrically before germ-line specification. J Cell Biol 149:875–888. Google Scholar


M. Köprunner, C. Thisse, B. Thisse, and E. Raz . 2001. A zebrafish nanos-related gene is essential for the development of primordial germ cells. Genes Dev 15:2877–2885. Google Scholar


S. Lin, W. Long, J. Chen, and N. Hopkins . 1992. Production of germ-line chimeras in zebrafish by cell transplants from genetically pigmented to albino embryos. Proc Natl Acad Sci USA 89:4519–4523. Google Scholar


A. Miyake, T. Saito, M. Kamimoto, T. Saito, T. Suzuki, N. Nakatsuji, and T. Nakatsuji . 2001. The vasa mRNA expression and localization during embryogenesis of the shiro-uo (Leucopsarion petersii). 14th International Congress of Developmental Biology supplement 43S121. Google Scholar


T. Mizuno, E. Yamaha, M. Wakahara, A. Kuroiwa, and H. Takeda . 1996. Mesoderm induction in zebrafish. Nature 383:131–132. Google Scholar


T. Mizuno, E. Yamaha, and F. Yamazaki . 1997. Localized axis determinant in the early cleavage embryo of the goldfish, Carassius auratus. Dev Genes Evol 206:389–396. Google Scholar


T. Mizuno, E. Yamaha, A. Kuroiwa, and H. Takeda . 1999. Removal of vegetal yolk causes dorsal deficencies and impairs dorsal-inducing ability of the yolk cell in zebrafish. Mech Dev 81:51–63. Google Scholar


T. Nagai, E. Yamaha, and K. Arai . 2001. Histological differentiation of primordial germ cells in zebrafish. Zool Sci 18:215–223. Google Scholar


T. Nakatsuji, T. Kitano, N. Akiyama, and N. Nakatsuji . 1997. Ice goby (shiro-uo), Leucopsarion petersii, may be useful material for studying teleostean embryogenesis. Zool Sci 14:443–448. Google Scholar


J. M. Oppenheimer 1936. The development of isolated blastoderms of Fundulus heteroclitus. J Exp Zool 72:247–269. Google Scholar


S. Otani, S. Maegawa, K. Inoue, K. Arai, and E. Yamaha . 2002. The germ cell lineage Identified by vas-mRNA during the embryogenesis in goldfish. Zool Sci 19:519–526. Google Scholar


A. Richards and J. T. Thompson . 1921. The migration of the primary sex-cells of Fundulus heteroclitus. Biol Bull 40:325–349. Google Scholar


T. Saito, M. Kamimoto, A. Miyake, E. Yamaha, T. Suzuki, N. Nakatsuji, and T. Nakatsuji . 2001. Mesoderm formation by isolated and cultivated 8-cell stage blastomeres of the teleost, Leucopsarion ptersii (shiro-uo). Int J Dev Biol 45:661–668. Google Scholar


Y. Takeuchi, G. Yoshizaki, and T. Takeuchi . 2001. Production of germ-line chimeras in rainbow trout by blastomere transplantation. Mol Reprod Dev 59:380–389. Google Scholar


L. P. M. Timmermans and N. Taverne . 1989. Segregation of primordial germ cells: their numbers and fate during early development of Barbus conchonius (Cyprinidae, Teleostei) as indicated by 3Hthymidine incorporation. Morphology 202:225–237. Google Scholar


T-C. Tung and Y-F. Y. Tung . 1944. The development of egg fragments, isolated blastomeres and fused eggs in the goldfish. Proc Zool Soc 114:46–64. Google Scholar


Y. Wakamatsu, K. Ozato, and T. Sasado . 1994. Establishment of a pluri-potent cell line derived from a medaka (Oryzias latipes) blastula embryo. Mol Mar Biol Biotechnol 3:185–191. Google Scholar


E. Yamaha, T. Mizuno, Y. Hasebe, H. Takeda, and F. Yamazaki . 1998. Dorsal specification in blastoderm at the blastula stage in the goldfish, Carassius auratus. Dev Growth Differ 40:267–275. Google Scholar


E. Yamaha, T. Mizuno, Y. Hasebe, and F. Yamazaki . 1997. Chimeric fish produced by exchanging upper parts of blastoderms in goldfish blastulae. Fisheries Sci 63:514–519. Google Scholar


E. Yamaha, T. Mizuno, K. Matsusita, and Y. Matsusita . 1999. Developmental staging in goldfish during the pre-gastrula stage. Nippon Suisan Gakkaishi 65:709–717. Google Scholar


C. Yoon, K. Kawakami, and N. Hopkins . 1997. Zebrafish vasa homologue RNA is localized to the cleavage planes of 2- and 4-cell-stage embryos and is expressed in the primordial germ cells. Development 124:3157–3165. Google Scholar
Taiju Saito, Satoshi Otani, Terumi Nagai, Takako Nakatsuji, Katsutoshi Arai, and Etsuro Yamaha "Germ Cell Lineage from a Single Blastomere at 8-Cell Stage in Shiro-uo (ice goby)," Zoological Science 19(9), 1027-1032, (1 September 2002).
Received: 18 April 2002; Accepted: 1 June 2002; Published: 1 September 2002
cell lineage
primordial germ cells (PGCs)
Back to Top