- Open Access
Sex-specific gene expression in preimplantation mouse embryos
© BioMed Central Ltd 2006
- Published: 1 March 2006
The 3.5-day-old blastocyst-stage mouse embryo consists of two tissues and contains approximately 60 cells. This tiny structure has now been observed to express nearly 600 genes in a sex-specific fashion, including at least one gene (Rhox/Pem) expressed only in females from their paternal X chromosome.
- Dosage Compensation
- Preimplantation Embryo
- Extraembryonic Tissue
- Male Embryo
- Preimplantation Stage
The daily deluge of marketing advertisements might have us believe that our entire lives are occupied with sex. Recent work from Kobayashi and colleagues  suggests that this may not be too far from the truth. It has long been observed that gene-expression differences correlated with genetic sex exist at the preimplantation stages. This was first observed 30 years ago, when it was noticed that 50% of eight-cell-stage mouse embryos expressed the histocompatibility Y (Hya) antigen. At the time these were correctly presumed to be the male embryos . Later work [3, 4] confirmed their prediction. Since then, several studies have confirmed the existence of a handful of genes that appear to be expressed in a sex-specific fashion in the preimplantation embryo (reviewed in ). Kobayashi et al.  recently increased that handful of genes by two orders of magnitude when they observed 591 transcripts that appeared to be differentially expressed in either male or female blastocysts.
To study sex-specific expression, they analyzed RNA derived from more than 1,000 sexed mouse blastocysts on a DNA microarray representing 20,000 transcripts . Although gene arrays have been used before with staged preimplantation embryos and have identified a complicated milieu of signaling pathways , they have not been used to look at differences between the sexes. To overcome the technical problem of correctly sexing so many embryos, Kobayashi et al.  used a strain of transgenic mice harboring a constitutively expressed X-linked green fluorescent protein (GFP) transgene (XGFP) . By breeding XGFPY transgenic males to non-transgenic (XX) females, female progeny could be distinguished at preimplantation stages from male littermates by their green fluorescence, which results from the zygotic expression of the paternally inherited GFP transgene. Male blastocysts, which have only a maternally inherited X chromosome, were identifiable by the lack of fluorescence.
While the identification of such a large number of genes with possible sexually dimorphic expression will provide much grist for the sex-determination field, this study will also provide material to pursue the mechanisms of autosomal and sex-chromosome imprinting - the preferential inactivation of genes according to maternal or paternal inheritance.
To test the validity of the assay, Kobayashi et al.  used reverse transcription PCR (RT-PCR) to confirm the sex-specific expression of the 11 genes that showed the greatest difference in expression between the sexes. Four of the 11 genes proved to be expressed in a sex-specific fashion, with between-sex expression differentials ranging from 2.5- to 14.8-fold. Although a number of autosomal loci were implicated as being differentially expressed in the study, the confirmation of expression patterns was carried out only for genes residing on the sex chromosomes.
In the diploid primordial germ cells of females, X inactivation occurs randomly , whereas in males both sex chromosomes undergo temporary transcriptional inactivation during meiosis [16, 17]. After fertilization, it is likely that these initial imprints are modified coincident with the onset of zygotic transcription at the two- to four-cell stage (Figure 1b). The emerging molecular model holds that two separate pathways enact this modification [10, 12, 18]. First, it appears likely that the paternal X chromosome is delivered to the unfertilized egg in a partially inactivated state (Figure 1a). This is supported by the observation that two-cell embryos have partially inactivated paternal X chromosomes . At this time a second pathway initiates a wave of de novo imprinting that acts upon the inactivated X through to the eight-cell stage to further impair its transcriptional activity (Figure 1c) . This inactivation is correlated with spreading of the Xist RNA, accumulation of hypermethylated histones, and localization of Polycomb group proteins along the inactivating X chromosome . Xist RNA is produced from the inactive X-specific transcripts (Xist) locus on inactivating X chromosomes and contributes to inactivation by binding progressively along the chromosome. Whether this de novo imprinting occurs after partial or complete removal of the imprints added in the sperm, or is simply layered on top of them, is uncertain. Thus, the level of inactivation of the paternal X chromosome increases through early development, possibly as a function of proximity of chromosomal regions to the paternally expressed Xist locus .
As the embryo begins to develop into a blastocyst, a new round of modifications occurs on the paternal X chromosome of those cells allocated to the inner cell mass , the precursor tissue of the embryo proper (Figure 1d). In these cells, the paternal X is reactivated, and dosage compensation is re-established in a random fashion. The trophectoderm cells, which have an extraembryonic fate, maintain paternal X inactivation.
This model does not rule out the presence of transcripts expressed from the paternal X chromosome and does not provide a mechanism for repression of the maternal allele of those transcripts. Thus, the finding by Kobayashi et al.  that Rhox5/Pem is expressed as a solely male transcript places it in a relatively rare class of genes including, most notably, Xist . An additional 16-20 genes that are expressed only from the allele on the paternal X chromosome have been putatively identified by gene-array screens comparing midgestation parthenogenetic and androgenetic embryos (which are engineered to contain either two maternal or two paternal genomes, respectively) . So far, however, the imprinted expression of Xist, and now Rhox5/Pem, are the only experimentally confirmed preimplantation examples of X-linked paternally expressed genes.
Rhox5/Pem is a member of the newly identified reproductive homeobox (Rhox) gene cluster. Like their better known Hox cluster cousins, the temporal and spatial order of expression of members of the Rhox cluster during gametogenesis correlates with their order on the X chromosome . Rhox5/Pem-deficient mice display male subfertility phenotypes [20, 21] consistent with the proposed role of Rhox proteins in gametogenesis. Given the imprinted expression of Rhox5/Pem, it will be interesting to examine whether other members of the Rhox cluster are expressed similarly in preimplantation embryos. As Rhox5/Pem is expressed during spermatogenesis, when the paternal X chromosome is acquiring its initial imprints, a detailed profile of Rhox5/Pem expression dynamics during spermatogenesis will undoubtedly be useful in determining the nature of the imprinting mechanism at this locus. In addition, as Xist-mediated inactivation occurs in a progressive manner, it will be important to look for correlations between the Rhox5/Pem expression dynamics in the preimplantation embryo and the expression of other genes between the Rhox5/Pem and Xist loci.
A couple of issues may cast a cloud over the observations made by Kobayashi and colleagues . As they note, in mice, male preimplantation-stage embryos develop more rapidly than females [22, 23]. Thus, some of the differentially expressed transcripts observed in the blastocysts sampled may represent artifacts produced by the slightly different developmental stages of the male and female embryos. Another complication could arise from the fact that the experiments were performed on in vitro cultured embryos. Previous work has established that imprinting may be perturbed during some in vitro conditions. For example, 65% of mouse embryos cultured in Whitten's medium, a commonly used mouse embryo culture medium, inappropriately expressed transcripts from the autosomal H19 locus, which is normally expressed only from the maternal allele, as well as from the X-linked Xist locus [24–26]. This aberrant imprinting was observed to persist through gastrulation , the last developmental stage tested. In fact, Kobayashi and colleagues  note that when the number of PCR cycles in the RT-PCRs were increased, a small amount of both Xist and Rhox5/Pem could be detected in male embryos (which do not contain a paternal X chromosome). The authors did control for this by looking at RT-PCR products from uncultured non-transgenic blastocysts; these blastocysts are, however, still subject to the same sex-related aging biases. Although the use of potassium simplex optimized medium (KSOM) in the present study probably avoids most of the artifactual gene expression seen with Whitten's medium, the expression signatures of individal genes will undoubtedly need to be confirmed in subsequent studies using embryos that have developed in vivo.
As often is the case, we are left with many open questions. As the Rhox cluster maps distantly from Xist, it is uncertain whether the imprinting of Rhox5/Pem is correlated with coating of this region by Xist RNA or whether it is repressed by another mechanism. From a developmental standpoint, the results of Kobayashi and colleagues  beg the question as to exactly which cells express Rhox5/Pem. Are the cells of the blastocyst expressing Rhox5/Pem from the paternal allele the ones fated to form specific tissues (such as the trophectoderm), where Rhox5/Pem will be expressed predominantly from the maternal chromosome? One intriguing observation  is that Rhox5/Pem is expressed specifically in extraembryonic tissues, the ones that are fated to inactivate their paternal X chromosome. Even so, the expression switch reported by Kobayashi and colleagues is intriguing, and may indeed present a model for looking at X-inactivation dynamics near the Rhox cluster in peri-implantation embryos.
This work has given us yet another glimpse of the breadth of genetic differences between the sexes, and in doing so has revealed an intriguing early developmental imprint to a gene known for its role in gametogenesis. Clearly much work remains to be done, but as the putatively differentially expressed genes are individually tested, it will be interesting to determine whether these sex-specific transcripts have sex-specific roles in these earliest of embryos. One might be tempted to fantasize that within their DNA array, Kobayashi and colleagues  may have at hand information to identify loci influencing our own sex-specific traits. But, sadly, we still have to wait for the final word on what differentiates blastocysts from their 'blasto-sisters'.
We thank Liz Lacy for insightful discussions and constructive comments.
- Kobayashi S, Isotani A, Mise N, Yamamoto M, Fujihara Y, Kaseda K, Nakanishi T, Ikawa M, Hamada H, Abe K, Okabe M: Comparison of gene expression in male and female mouse blastocysts revealed imprinting of the x-linked gene, rhox5/pem, at preimplantation stages. Curr Biol. 2006, 16: 166-172. 10.1016/j.cub.2005.11.071.PubMedView ArticleGoogle Scholar
- Krco CJ, Goldberg EH: H-Y male antigen: detection on eight-cell mouse embryos. Science. 1976, 193: 1134-1135.PubMedView ArticleGoogle Scholar
- Epstein CJ, Smith S, Travis B: Expression of H-Y-antigen on pre-implantation mouse embryos. Tissue Antigens. 1980, 15: 63-67.PubMedView ArticleGoogle Scholar
- White KL, Lindner GM, Anderson GB, BonDurant RH: Survival after transfer of "sexed" mouse embryos exposed to H-Y antisera. Theriogenology. 1982, 6: 655-662. 10.1016/0093-691X(82)90031-0.View ArticleGoogle Scholar
- Morison IM, Ramsay JP, Spencer HG: A census of mammalian imprinting. Trends Genet. 2005, 21: 457-465. 10.1016/j.tig.2005.06.008.PubMedView ArticleGoogle Scholar
- Wang QT, Piotrowska K, Ciemerych MA, Milenkovic L, Scott MP, Davis RW, Zernicka-Goetz M: A genome-wide study of gene activity reveals developmental signaling pathways in the preimplantation mouse embryo. Dev Cell. 2004, 6: 133-144. 10.1016/S1534-5807(03)00404-0.PubMedView ArticleGoogle Scholar
- Hadjantonakis AK, Gertsenstein M, Ikawa M, Okabe M, Nagy A: Non-invasive sexing of preimplantation stage mammalian embryos. Nat Genet. 1998, 19: 220-222. 10.1038/893.PubMedView ArticleGoogle Scholar
- Takagi N, Sasaki M: Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse. Nature. 1975, 256: 640-642. 10.1038/256640a0.PubMedView ArticleGoogle Scholar
- West JD, Frels WI, Chapman VM, Papaioannou VE: Preferential expression of the maternally derived X chromosome in the mouse yolk sac. Cell. 1977, 12: 873-882. 10.1016/0092-8674(77)90151-9.PubMedView ArticleGoogle Scholar
- Huynh KD, Lee JT: X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny. Nat Rev Genet. 2005, 6: 410-418. 10.1038/nrg1604.PubMedView ArticleGoogle Scholar
- Okamoto I, Arnaud D, Le Baccon P, Otte AP, Disteche CM, Avner P, Heard E: Evidence for de novo imprinted X-chromosome inactivation independent of meiotic inactivation in mice. Nature. 2005, 438: 369-373. 10.1038/nature04155.PubMedView ArticleGoogle Scholar
- Huynh KD, Lee JT: Inheritance of pre-inactivated paternal X chomrosome in early mouse embryos. Nature. 2003, 426: 857-862. 10.1038/nature02222.PubMedView ArticleGoogle Scholar
- Okamoto I, Otte AP, Allis CD, Reinberg D, Heard E: Epigenetic dynamics of imprinted X inactivation during early mouse development. Science. 2004, 303: 644-649. 10.1126/science.1092727.PubMedView ArticleGoogle Scholar
- Mak W, Nesterova TB, de Napoles M, Appanah R, Yamanaka S, Otte AP, Brockdorff N: Reactivation of the paternal X chromosome in early mouse embryos. Science. 2004, 303: 666-669. 10.1126/science.1092674.PubMedView ArticleGoogle Scholar
- McMahon A, Fosten M, Monk M: Random X-chromosome inactivation in female primordial germ cells in the mouse. J Embryol Exp Morphol. 1981, 64: 251-258.PubMedGoogle Scholar
- Baarends WM, Wassenaar E, van der Laan R, Hoogerbrugge J, Sleddens-Linkels E, Hoeijmakers JH, de Boer P, Grootegoed JA: Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis. Mol Cell Biol. 2005, 25: 1041-1053. 10.1128/MCB.25.3.1041-1053.2005.PubMedPubMed CentralView ArticleGoogle Scholar
- Turner JM, Mahadevaiah SK, Fernandez-Capetillo O, Nussenzweig A, Xu X, Deng CX, Burgoyne PS: Silencing of unsynapsed meiotic chromosomes in the mouse. Nat Genet. 2005, 37: 41-47.PubMedGoogle Scholar
- Reik W, Ferguson-Smith AC: Developmental biology: the X-inactivation yo-yo. Nature. 2005, 438: 297-298. 10.1038/438297a.PubMedView ArticleGoogle Scholar
- Nikaido I, Saito C, Mizuno Y, Meguro M, Bono H, Kadomura M, Kono T, Morris GA, Lyons PA, Oshimura M, et al: Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling. Genome Res. 2003, 13: 1402-1409. 10.1101/gr.1055303.PubMedPubMed CentralView ArticleGoogle Scholar
- Maclean JA, Chen MA, Wayne CM, Bruce SR, Rao M, Meistrich ML, Macleod C, Wilkinson MF: Rhox: a new homeobox gene cluster. Cell. 2005, 120: 369-382. 10.1016/j.cell.2004.12.022.PubMedView ArticleGoogle Scholar
- Pitman JL, Lin TP, Kleeman JE, Erickson GF, MacLeod CL: Normal reproductive and macrophage function in Pem homeobox gene-deficient mice. Dev Biol. 1998, 202: 196-214. 10.1006/dbio.1998.8978.PubMedView ArticleGoogle Scholar
- Tsunoda Y, Tokunaga T, Sugie T: Altered sex ratio of live young after transfer of fast- and slow-developing mouse embryos. Gamete Res. 1985, 12: 301-304. 10.1002/mrd.1120120308.View ArticleGoogle Scholar
- Zwingman T, Erickson RP, Boyer T, Ao A: Transcription of the sex-determining region genes Sry and Zfy in the mouse preimplantation embryo. Proc Natl Acad Sci USA. 1993, 90: 814-817.PubMedPubMed CentralView ArticleGoogle Scholar
- Sasaki H, Ferguson-Smith AC, Shum AS, Barton SC, Surani MA: Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. Development. 1995, 121: 4195-4202.PubMedGoogle Scholar
- Doherty AS, Mann MR, Tremblay KD, Bartolomei MS, Schultz RM: Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo. Biol Reprod. 2000, 62: 1526-1535. 10.1095/biolreprod62.6.1526.PubMedView ArticleGoogle Scholar
- Mann MR, Lee SS, Doherty AS, Verona RI, Nolen LD, Schultz RM, Bartolomei MS: Selective loss of imprinting in the placenta following preimplantation development in culture. Development. 2004, 131: 3727-3735. 10.1242/dev.01241.PubMedView ArticleGoogle Scholar