Abstract
In early mammalian embryos, the genome is transcriptionally quiescent until the zygotic genome activation (ZGA) which occurs 2-3 days after fertilization. Despite a long-standing effort, maternal transcription factors regulating this crucial developmental event remain largely elusive. Here, using maternal and paternal mouse models of Yap1 deletion, we show that maternally accumulated yes-associated protein (YAP) in oocyte is essential for ZGA. Maternal Yap1-knockout embryos exhibit a prolonged two-cell stage and develop into the four-cell stage at a much slower pace than the wild-type controls. Transcriptome analyses identify YAP target genes in early blastomeres; two of which, Rpl13 and Rrm2, are required to mediate maternal YAP's effect in conferring developmental competence on preimplantation embryos. Furthermore, the physiological YAP activator, lysophosphatidic acid, can substantially improve early development of wild-type, but not maternal Yap1-knockout embryos in both oviduct and culture. These observations provide insights into the mechanisms of ZGA, and suggest potentials of YAP activators in improving the developmental competence of cultured embryos in assisted human reproduction and animal biotechnology.
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Introduction
Mammalian oocytes, upon fertilization, are reprogrammed from a highly specialized, non-proliferative, meiotic state to totipotent, mitotic embryos, which subsequently gain the ability to proliferate, differentiate and develop into new individuals1,2. A critical step in early development is the maternal-zygotic transition (MZT) occurring 2-3 days after fertilization in mice, which is controlled by maternally deposited RNAs and proteins3,4. Initially, the zygotic genome is transcriptionally quiescent; however, after MZT, the zygotic genome becomes active and takes control of development5,6. There is a long-standing question as which maternal factors regulate MZT, and, particularly, which maternal transcription factor(s) regulate zygotic genome activation (ZGA).
Clinically, many in vitro matured human oocytes exhibit developmental arrest at different stages after fertilization, owing to genetic variations or in some cases, inappropriate culture conditions7,8,9. Therefore, understanding the maternal factors and molecular mechanisms underpinning the developmental competence of preimplantation embryos is significant to the improvement of the success rate in assisted reproductive technology.
The zinc-finger protein Zelda is a key activator of the early zygotic genome in Drosophila10. However, the gene encoding this protein (Zld) is not conserved in mammals, indicating that different genes or mechanisms may be involved. Transcriptome analyses has revealed that Yap1, which encodes the yes-associated protein (YAP), is highly expressed in human and mouse oocytes and early embryos11,12. YAP is a transcriptional co-activator of TEAD family transcriptional factors (TEAD1-4)13,14. Zygotically expressed TEAD4 is required for the specification of trophectoderm (TE) and inner cell mass (ICM) in blastocysts by inducing the expression of CDX2 in TE cells15,16. However, the maternal functions of YAP and TEADs in oocyte development and MZT have not been investigated.
In this study, we used maternal and paternal mouse models of Yap1 deletion to elucidate the function of maternal YAP in ZGA. By targeting the expression of key early zygotic genes, maternal YAP renders preimplantation embryos developmentally competent. Furthermore, the physiological YAP activator, lysophosphatidic acid (LPA), stimulates early embryonic development. These observations provide insights into the mechanisms of ZGA in mammals, and offer potential new approaches in assisted reproductive technology.
Results
Yap1 is highly expressed in mammalian oocytes and early embryos
By comparing the transcriptomes of human/mouse oocytes and somatic cells, we found that the transcription coactivator Yap1 is predominantly expressed in oocytes and preimplantation embryos, but the other TEAD coactivator Taz is not (Figure 1A and 1B). This observation suggests that YAP may have an important role in ZGA.
Immunofluorescent staining revealed that YAP is expressed in mouse oocytes and early embryos; however, the subcellular distribution varies (Figure 1C and 1D). YAP is evenly distributed in oocytes at germinal vesicle (GV) stage, but is gradually translocated from cytoplasm to nucleus after fertilization. At the morula and blastocyst stages, the nuclei of outer layer blastomeres accumulate significantly higher levels of YAP than inner layer blastomeres (Figure 1C and 1D).
Contributions of maternal and paternal Yap1 expression to early embryonic development
To investigate the function of YAP in mouse oocytes, we selectively deleted Yap1 in oocytes by crossing Yap1fl/fl mice with transgenic Gdf9-Cre mice17,18. YAP expression in oocytes is abolished in Yap1fl/fl;Gdf9-Cre females (Figure 1E-1G). We then studied the development of zygotes derived from Yap1-knockout oocytes. When fertilized by wild-type (WT) spermatozoa, the resulting maternal Yap1-knockout embryos (Yap1♀−/♂+) had a prolonged two-cell stage and developed into the four-cell stage at a much slower rate when compared with that of WT controls (Yap1♀+/♂+; Figure 2A-2C). About two-thirds (63.4%) of the Yap1♀−/♂+ embryos died before compaction. Only 28.8% of Yap1♀−/♂+ embryos developed to the blastocyst stage (Figure 2D).
We further analyzed the fertility of Yap1fl/fl;Gdf9-Cre females by crossing them to adult WT males. In a 6-month fertility test, Yap1fl/fl;Gdf9-Cre females were subfertile and produced only 2.74 ± 0.24 pups per litter, whereas WT littermates produced 7.97 ± 0.37 pups per litter on average (Figure 2E and 2F). Yap1fl/fl;Gdf9-Cre females also exhibited a progressive loss in fertility — they gave birth to 3-5 pups in the first 1-2 litters but gradually produced fewer pups or even became infertile (Figure 2F).
Because the paternal Yap1 allele is intact in Yap1♀−/♂+ embryos, we analyzed the expression of YAP in these embryos (Figure 2G-2J). YAP is weakly expressed in Yap1♀−/♂+ embryos at four- and eight-cell stages (Figure 2I and 2J). Notably, YAP expression was restored in blastocysts developed from maternal Yap1-deleted zygotes (Figure 2G). These results suggest that the expression of paternal Yap1 rescues the developmental defects in some embryos (Figure 2A). To test this hypothesis, we developed Yap1fl/−;Ddx4-Cre mice, with Yap1 knockout in the male germline. Yap1fl/−;Ddx4-Cre males were fertile and had normal spermatogenesis (Supplementary information, Figure S1). Yap1fl/fl;Gdf9-Cre females were infertile when mated to these males. YAP expression was completely ablated in Yap1♀−/♂− embryos (Figure 2A and 2H-2J), which exhibit severe developmental defects (Figure 2C). Specifically, Yap1♀−/♂− embryos had significant growth retardation at two to four-cell stages, and their development was blocked completely before compaction (Figure 2C and 2D).
Owing to the known functions of YAP in cell proliferation, apoptosis and tumorigenesis, YAP may play a role in normal ovarian development and function19,20,21,22. Surprisingly, oocyte-specific deletion of YAP did not affect primordial follicle formation, activation and folliculogenesis. Yap1fl/fl;Gdf9-Cre females ovulated normal MII oocytes with well-organized spindles (Supplementary information, Figure S2). Moreover, the ovaries of Yap1fl/fl;Gdf9-Cre females contained similar number of developing follicles as those of WT females. Aged (7 months old) Yap1fl/fl;Gdf9-Cre females did not show signs of premature ovarian failure (Supplementary information, Figure S2B). These results indicate that, despite its important functions in somatic cells, YAP is dispensable for the survival, growth and maturation of mouse oocytes.
Fertilization and pronucleus formation were not affected by maternal YAP deletion (Figure 3A and 3B). Phosphorylated RNA polymerase II at serine-2 (pS2, a marker of RNA polymerase II activation, Figure 3C) and trimethylated histone H3 at lysine-4 (H3K4me3, a histone modification that facilitates transcription, Figure 3D) were not affected by maternal YAP deletion.
By embryonic day 3.5 (E3.5), normal blastocysts contain two types of cells: TE cells and ICM cells. Because most maternal YAP-deleted embryos failed to develop into blastocysts, we investigated whether the blastomeres in the developmentally arrested embryos acquired a TE cell fate or an ICM cell fate. Caudal type homeobox 2 (CDX2) is a functional marker for the TE, whereas the pluripotency-associated transcription factors Oct4 and Nanog are functional markers for the ICM. Few blastomeres in Yap1♀−/♂+ embryos expressed CDX2; instead, most blastomeres of Yap1-deleted embryos expressed Nanog and OCT4 (Figure 3E and 3F). These results indicate that maternal YAP is required for proper differentiation of TE; in the absence of maternal YAP most blastomeres adopt an ICM cell fate.
Identifying target genes of maternal YAP during zygotic genome activation
To identify the YAP target genes in early embryos, we profiled the transcriptomes of GV oocytes and four-cell stage embryos derived from WT and Yap1fl/fl;Gdf9-Cre females (Figure 4A and Supplementary information, Figure S3A). Consistent with the inactive state of YAP in GV oocytes, transcriptomes of GV oocytes derived from WT and Yap1fl/fl;Gdf9-Cre females were similar (Supplementary information, Figure S3B). There were only 186 transcripts downregulated and 87 transcripts upregulated in YAP-deleted oocytes. However, at the four-cell stage, the transcriptome of Yap1♀−/♂+ embryos was significantly different from that of WT embryos: 1 292 transcripts were downregulated, and 2 826 were upregulated in Yap1♀−/♂+ four-cell embryos (Figure 4B).
Gene ontology (GO) analyses revealed that many of the upregulated transcripts were associated with cell cycle (Supplementary information, Figure S3C). This is consistent with the prolonged two-cell stage and delayed embryogenesis upon Yap1 deletion. During MZT, many maternal transcripts are degraded in WT embryos to facilitate ZGA. Strikingly, 79.7% (2 254 in 2 826) of the transcripts upregulated in Yap1♀−/♂+ embryos during the GV to four-cell transition were genes that would have been degraded in WT embryos (Supplementary information, Figure S3D). If only the top 10% abundant transcripts in oocytes are considered, 95.5% of the upregulated transcripts in Yap1♀−/♂+ embryos evaded degradation that is their normal fate (Figure 4C and Supplementary information, Figure S3D), indicating the importance of maternal YAP in MZT. Expression of representative transcripts is shown in Figure 4D and Supplementary information, Figure S3E.
On the other hand, the downregulated transcripts in Yap1♀−/♂+ embryos were significantly associated with protein translation (Figure 4E). Among these, 704 transcripts are upregulated during ZGA in WT embryos (from zygote stage to four-cell stage). These genes are potentially the YAP-TEAD-targeted early zygotic genes. When compared with published ChIP results of YAP in mouse embryonic stem cells42, 23 genes were found to be YAP targets in early mouse embryos (Supplementary information, Table S1, FPKM (fragments per kilobase of transcript per million mapped reads) > 10 in WT embryos at four-cell stage). The mRNA levels of selected genes in WT and Yap1♀−/♂+ embryos determined by quantitative real-time PCR (qRT-PCR) (Figure 4F) were largely consistent with the RNA-seq data.
Among the 23 genes, Rpl13 (ribosomal protein L13), Rrm2 (ribonucleotide reductase M2), Alppl2 (alkaline phosphatase 2), Sfn (stratifin), Slc39a4 (solute carrier family 39, member 4) and Tead4 contain 1-3 putative TEAD-binding sites within 2 000 bp upstream of their transcription start sites23. All these genes were downregulated in Yap1♀−/♂+ four-cell embryos (Figure 4F). In luciferase assay, promoters of Rpl13 and Rrm2 elicited strong responses to YAP-TEAD1 and YAP-TEAD4 (Figure 5A), but not to a YAP mutant that lacks affinity for TEADs (Figure 5B and 5C). Overexpression of YAP-TEAD1 in GV oocytes also increased the expression of Rpl13 and Rrm2, as well as other putative YAP target genes (Bzw2, Klf2 and Ncl; Figure 5D).
Rpl13 and Rrm2 are among the early expressed genes in human and mouse embryos (Supplementary information, Figure S4). Rpl13 encodes a ribosomal protein that promotes protein translation; Rrm2 encodes an essential component of ribonucleotide reductase that catalyzes the biosynthesis of deoxyribonucleotides24. The induction of these two genes by YAP-TEAD might improve the developmental competence of early embryos by increasing protein translation and DNA synthesis. Indeed, combined depletion of Rpl13 and Rrm2 in WT zygotes reduced the developmental competence of embryos (Figure 5E-5G). The Rpl13- and Rrm2-depleted embryos were arrested at the morula stage before compaction (Figure 5F). This defect phenocopied that observed in the Yap1♀−/♂+ embryos. The expression of YAP target genes was compromised in Rpl13- and Rrm2-depleted embryos, as shown by qRT-PCR results (Figure 5H). Taken together, maternal YAP is activated in early embryos and transcriptionally activate Rpl13 and Rrm2, which critically regulate developmental competence.
LPA stimulates early embryogenesis by activating YAP
In cultured cell lines, YAP activity and its subcellular distribution are controlled by the Hippo pathway25. LPA inhibits the Hippo pathway components LATS1/2, and therefore activates YAP26. LPA is present in many animal biological fluids including oviduct tubal fluid27. Significant nuclear localization of YAP was observed in four-cell embryos collected from the oviducts, but not in those cultured in vitro (Figure 6A and 6B). However, LPA treatment promoted YAP nuclear localization, as well as expression of downstream genes in cultured embryos (Figure 6B-6E). These results suggest that LPA activates YAP in early embryos in vivo.
M16 medium is widely used in oocyte culture but barely supports embryonic development (Figure 6F). Adding LPA to M16 medium significantly increased the development rates of WT embryos, but this effect was not observed in Yap1♀−/♂+ embryos (Figure 6F and 6G). In an embryo transfer experiment, foster mothers transferred with LPA-treated embryos gave birth to more pups than fosters that received control-treated embryos (Figure 6H). These results suggest that LPA improves the developmental competence of preimplantation embryos by activating YAP and its downstream genes (Figure 7).
Discussion
The involvement of YAP-TEAD in mouse embryonic development has been reported15,16,28,29. However, the contribution of maternal Yap1 mRNA and protein was less clear before our study. Here we demonstrate a detrimental effect of maternal YAP deletion at two- to four-cell stage, and identify critical YAP-TEAD target genes in early embryos (Figure 7). Conventional Yap1 knockout results in developmental defects at E8.5 without affecting preimplantation development29. This suggests that maternal YAP stored in oocytes by Yap+/− mother is sufficient to support development beyond the early stages. In addition, although YAP was reported to be important for survival, proliferation and differentiation in a wide range of somatic cell types, germ cell-specific Yap1 knockout affected neither oogenesis nor spermatogenesis. Our observations highlight the developmental stage-specific role of maternal YAP in ZGA, and zygotic Yap1 as an early zygotic gene required for embryogenesis when the maternal YAP is exhausted at the approximately four-cell stage.
The functions of YAP-TEAD and the upstream Hippo pathway have been reported in many cell types including embryonic stem cells; however, YAP target genes in specific physiological contexts are less understood. The most studied TEAD4 target gene in preimplantation embryos is Cdx2, which is crucial for TE specification15,30,31. But the defects in maternal YAP-depleted embryos occur as early as the two- to four-cell stage, at which time CDX2 is absent. This suggests that maternal YAP targets other early-expressed zygotic genes. By comparing the transcriptomes between WT and Yap1♀−/♂+ mouse embryos, we have now identified novel YAP-TEAD-regulated early zygotic genes. Among them Rpl13 and Rrm2 are direct target of YAP-TEADs. RPL13 and RRM2 may implement YAP's effect by promoting protein and DNA synthesis immediately after ZGA. Depletion of them in zygotes causes defects similar to maternal YAP deletion. Thus, expression of Rpl13 and Rrm2 may be used as a new criterion in evaluating developmental competence of early mammalian embryos.
LPA has been reported to improve the developmental competence of cultured bovine embryos, but the underlying mechanism(s) was unclear32,33,34,35. Although LPA is known to activate YAP by inhibiting the Hippo pathway in cultured cell lines, a physiological context for this regulation has been lacking. Here we show YAP can mediate LPA's effect in improving the developmental competence of preimplantation embryos. LPA binds to albumin with high affinity and exists in most of commercial serum or albumin products26,36. Albumin is routinely added in human and mouse embryo culture media37,38,39. The protein-bound LPA, instead of albumin itself, may be the key bioactive molecule to support in vitro embryonic development. Considering that serum products are prone to contamination by unknown pathogens, LPA is a plausible and potentially safer substitute in making chemically defined embryo culture media. This justifies further investigation before LPA is to be adopted in human assisted reproductive medicine.
Materials and Methods
Mice
Yap1fl/fl mice17 were a gift from Dr Duojia Pan and were crossed with Gdf9-Cre40 or Ddx4-Cre41 transgenic mice. Primers used for genotyping are listed in Supplementary information, Table S2. Animal care and experimental procedures were in accordance with the Animal Research Committee guidelines of Zhejiang University.
Oocyte culture and microinjection
Twenty-one-day-old mice were injected with pregnant mare's serum gonadotropin (PMSG) and were euthanized 44 h later. Oocytes at GV stage were cultured in mini-drops of M16 medium (M7292; Sigma-Aldrich) covered with mineral oil at 37 °C in 5% CO2. For microinjection, mRNAs were in vitro transcribed using SP6 message machine kit (Invitrogen, AM1450). siRNA was obtained from GenePharma and the sequences are shown in Supplementary information, Table S2. Microinjection of oocytes was performed using an Eppendorf microinjector.
Superovulation, fertilization and embryo culture
Pubertal female mice (21-23 days old) were intraperitoneally injected with 5 IU PMSG for 44 h and followed by 5 IU human chorionic gonadotropin (hCG). Sixteen h after the second injection, cumulus-oocyte complexes were collected from oviducts. To obtain early embryos, female mice were mated with adult WT males overnight after hCG administration. Zygotes and embryos were collected from oviducts or uteri at indicated time points post-hCG injection, and cultured in KSOM (Sigma-Aldrich). For the experiments related to LPA treatments, zygotes were cultured in M16 with or without adding 10 μM LPA. Embryo morphology was observed and images were acquired using a Nikon SMZ1500 stereoscope.
Embryo transfer
Zygotes were collected as described above and were cultured in M16 with or without adding 10 μM LPA for 80 h. Next, the embryos were transferred into the uteri of pseudopregnant ICR female mice (15 embryos per mouse). The litter sizes were determined at birth.
RNA extraction and qRT-PCR
Total RNA was extracted using RNeasy Mini kit (Qiagen) according to the manufacturer's instructions. qRT-PCR analyses were performed using a Power SYBR Green PCR Master Mix (Life technologies) on an Applied Biosystems 7500 PCR System. Relative mRNA levels were calculated by normalizing to the levels of endogenous Gapdh mRNA (internal control) using Microsoft EXCEL. For each experiment, qPCR reactions were done in triplicate. Primer sequences are listed in Supplementary information, Table S2.
RNA-seq and library construction
GV oocytes and four-cell embryos were collected from WT and Yap1fl/fl;Gdf9-Cre mice (100 oocytes or embryos per sample). Total RNA was extracted from the samples using the RNeasy Plus Micro kit (Qiagen) following the manufacturer's protocol. Before RNA isolation, 2 × 106 mRNA-RFP was added to calculate mRNA copy number in each sample. Extracted total RNA was used to build a sequencing library using the NEB Next Ultra RNA Library Prep Kit for Illumina. We sequenced the library by Illumina Hiseq 2500 and aligned RNA-seq reads to Mus musculus UCSC mm9 references with the Tophat software (http://tophat.cbcb.umd.edu/), and calculated the FPKM of each gene using Cufflinks (http://cufflinks.cbcb.umd.edu). The amount of total mRNA was calculated based on the FPKM of exogenous RFP. GO analysis for enrichment of genes was determined using the Database for Annotation, Visualization and Integrated Discovery. The RNA-seq data have been deposited in Gene Expression Omnibus under the accession number GSE74344.
Confocal microscopy
Oocytes and embryos were fixed for 30 min in 4% paraformaldehyde dissolved in PBS. After blocking in 1% BSA in PBS, oocytes were incubated with primary antibodies diluted in the blocking solution for 1 h. After three washes, oocytes were incubated with secondary antibodies for 30 min, and then counterstained with 5 μg/ml 4′,6-diamidino-2-phenylindole or propidium iodide for 10 min. Oocytes were mounted and examined with a confocal laser scanning microscope (Zeiss LSM 710, Carl Zeiss AG, Germany). The primary antibodies used are listed in Supplementary information, Table S3.
Western blot analysis
Total protein extract from 100 oocytes was separated by SDS-PAGE and transferred to PVDF membranes (Millipore). After incubation with primary antibodies and an HRP-linked secondary antibody, bands on the membranes were detected using an Enhanced Chemiluminescence Detection Kit (Amersham). Antibodies and the dilutions used are indicated in Supplementary information, Table S3.
Histological analysis
Formalin-fixed, paraffin-embedded samples were sectioned at 5-μm thickness and stained with hematoxylin and eosin. For immunofluorescent staining, sections were sequentially probed with primary antibodies and conjugated secondary antibodies (Molecular Probes). Digital images were acquired using an epifluorescent microscope (Nikon Eclipse 80i). Antibodies used are listed in Supplementary information, Table S3.
Cell culture, plasmid transfection and luciferase assay
HEK293 cells were grown in DMEM (Invitrogen) supplemented with 10% fetal bovine serum. Transient plasmid transfections were done using Lipofectamine 2000 (Invitrogen). For luciferase assay, cells were transfected with luciferase reporters with or without plasmids encoding components of YAP-TEAD complex. Expression of Renilla luciferase was served as loading control. After 48 h, cells were lysed in Passive Lysis Buffer (Promega) and subjected to luciferase assay following the manufacturer's instructions (Dual luciferase system, Promega).
Statistical analysis
Results are given as means ± SEM; each experiment included at least three independent samples and was repeated at least three times. Group comparisons were made by two-tailed unpaired Student's t-tests. *P < 0.05; **P < 0.01, and ***P < 0.001.
Author Contributions
CY, SYJ, QQS, JJZ, YFY and LYY conducted experiments. YD and FT conducted informatics analyses of RNA sequencing results. JQ, FT and HYF conceived and designed the experiments and wrote the paper.
Competing Financial Interests
The authors declare no conflict of interest.
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Acknowledgements
We thank Dr. Duojia Pan for Yap1 flox mice. This study was funded by the National Basic Research Program of China (2012CB944403) and the National Natural Science Foundation of China (81172473, 91519313 and 31371449).
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( Supplementary information is linked to the online version of the paper on the Cell Research website.)
Supplementary information
Supplementary information, Figure S1
YAP deletion in male germ cells has few effects on male fertility. (PDF 679 kb)
Supplementary information, Figure S2
YAP is dispensable for survival, growth, and maturation of mouse oocytes. (PDF 631 kb)
Supplementary information, Figure S3
Trasnscriptome profiling of WT and YAP-deleted oocytes and 4-cell embryos. (PDF 691 kb)
Supplementary information, Figure S4
mRNA level of Rpl13 and Rrm2 in preimplantational embryos. (PDF 570 kb)
Supplementary information, Table S1
Gene description. (PDF 76 kb)
Supplementary information, Table S2
Primer sequences (PDF 97 kb)
Supplementary information, Table S3
Antibody information (PDF 64 kb)
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Yu, C., Ji, SY., Dang, YJ. et al. Oocyte-expressed yes-associated protein is a key activator of the early zygotic genome in mouse. Cell Res 26, 275–287 (2016). https://doi.org/10.1038/cr.2016.20
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DOI: https://doi.org/10.1038/cr.2016.20
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The function of Nucleoporin 37 on mouse oocyte maturation and preimplantation embryo development
Journal of Assisted Reproduction and Genetics (2022)
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Argonaute 2 is a key regulator of maternal mRNA degradation in mouse early embryos
Cell Death Discovery (2020)
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Dynamics and clinical relevance of maternal mRNA clearance during the oocyte-to-embryo transition in humans
Nature Communications (2020)
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An integrated genome-wide multi-omics analysis of gene expression dynamics in the preimplantation mouse embryo
Scientific Reports (2019)