Endogenous retroviruses (ERVs) are remnants of ancient retroviral infections, and comprise nearly 8% of the human genome1. The most recently acquired human ERV is HERVK(HML-2), which repeatedly infected the primate lineage both before and after the divergence of the human and chimpanzee common ancestor2,3. Unlike most other human ERVs, HERVK retained multiple copies of intact open reading frames encoding retroviral proteins4. However, HERVK is transcriptionally silenced by the host, with the exception of in certain pathological contexts such as germ-cell tumours, melanoma or human immunodeficiency virus (HIV) infection5,6,7. Here we demonstrate that DNA hypomethylation at long terminal repeat elements representing the most recent genomic integrations, together with transactivation by OCT4 (also known as POU5F1), synergistically facilitate HERVK expression. Consequently, HERVK is transcribed during normal human embryogenesis, beginning with embryonic genome activation at the eight-cell stage, continuing through the emergence of epiblast cells in preimplantation blastocysts, and ceasing during human embryonic stem cell derivation from blastocyst outgrowths. Remarkably, we detected HERVK viral-like particles and Gag proteins in human blastocysts, indicating that early human development proceeds in the presence of retroviral products. We further show that overexpression of one such product, the HERVK accessory protein Rec, in a pluripotent cell line is sufficient to increase IFITM1 levels on the cell surface and inhibit viral infection, suggesting at least one mechanism through which HERVK can induce viral restriction pathways in early embryonic cells. Moreover, Rec directly binds a subset of cellular RNAs and modulates their ribosome occupancy, indicating that complex interactions between retroviral proteins and host factors can fine-tune pathways of early human development.
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Gene Expression Omnibus
Sequencing data sets generated for this study are deposited under in the Gene Expression Omnibus under accession number GSE63570. Reprints and permissions information is available at www.nature.com/reprints. The authors declare no competing financial interests. Readers are welcome to comment on the online version of the paper. Correspondence and requests formaterials should be addressed to J.W. (email@example.com).
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We thank P. Bieniasz for the HERVK-con plasmid, P. Lovelace for assistance with FACS, M. Teruel for recombinant Giardia DICER, J. Perrino for TEM assistance, T. Swigut for ideas and input on data analysis, B. Gu for assistance with bisulfite sequencing, A. Moore for assistance with influenza experiments, J. Skowronski and members of the Wysocka laboratory for invaluable comments on the manuscript. This work was supported by the National Institutes of Health (NIH) P01 GM099130 and R01 GM112720 (J.W.); Stanford Genome Sciences Training Program and National Science Foundation Graduate Research Fellowship Program (E.J.G.); NIH F30 (1F30CA189514-01) (R.A.F.); NIH DP2AI11219301 (C.A.B.); Smith Family Stanford Graduate Fellowship (N.L.B.); CIRM RB4-05763 and NIH P50-HG007735 (H.Y.C.); CIRM RB3-02209, March of Dimes 6-FY10-351 and U01 HL100397 (R.A.R.P.) grants and NIH equipment grants 1S10RR02933801 (Institute for Stem Cell Biology and Regenerative Medicine FACS core) and 1S10RR02678001 (electron microscopy core facility).
The authors declare no competing financial interests.
Extended data figures and tables
Extended Data Figure 1 Additional single-cell RNA-seq data analyses from preimplantation human embryos (supporting Fig. 1).
a, Heat map and hierarchical K-means clustering of highly expressed (average RPKM > 6 across 89 embryo libraries) repetitive elements in single cells of human preimplantation embryos at indicated developmental stages (top) and HERVK expression (bottom) using indicated data sets. b, HERVH expression (RPKM) in single cells of human embryos at indicated preimplantation stages. Solid line indicates mean. RNA-seq data are taken from ref. 10. c, HERVH expression (RPKM) in single cells of human blastocysts, grouped by lineage. Solid line indicates mean. Oocyte (n = 3), zygote (n = 3), 2-cell (n = 6), 4-cell (n = 11), 8-cell (n = 19), morula (n = 16), TE (n = 18), PE (n = 7), EPI (n = 5), p0 (n = 8), p10 (n = 26). RNA-seq data set was from ref. 10. d, Genome browser snapshot showing 100 bp PE-RNA-seq reads from ELF1 naive human EScells aligning at the HERVK 108 provirus on chromsome 7.
Extended Data Figure 2 LTR5 alignments, HERVK expression data in cell lines, and control ChIP-qPCR analyses in primed human ES cells (supporting Fig. 2).
a, Top, presence of HERVK(HML-2) sequences in Old World primates, but absence in New World primates. Middle, schematic of HERVK proviral genome; all human-specific insertions contain LTR5HS. Bottom, phylogenetic relationship of HERVK LTR subclasses showing high degree of sequence similarity. Pro, protease; Pol, polymerase; Gag, group-specific antigen; Env, envelope. Bottom, ClustLW multiple sequence alignment of indicated HERVK LTR sequences (top), region around OCT4 motif is boxed, phylogenetic tree (bottom) indicating presence/absence of OCT4 motif. b, HERVK protein expression in human EC cells and human ES cells. Protein extracts from human EC cells (NCCIT) and human ES cells (H9) were analysed by immunoblotting with an antibody detecting HERVK Gag precursor and the processed Capsid (top), or the glycosylated, unprocessed form of the HERVK envelope protein Env (bottom). Tata-binding protein (TBP) was used as a loading control. Shown is a representative result of three independent experiments. c, RT–qPCR analysis of HERVK RNA expression in human EC cell line NCCIT, human ES cell line H9, and HEK293 cells. Three distinct qPCR amplicons, corresponding to env, gag and pro are shown. Samples were normalized to 18S ribosomal RNA levels. *P value < 0.05, one-sided t-test. Error bars are ±1 s.d., n = 3 biological replicates. d, HERVK gag or env expression in male human ES cell lines HSF-1, HSF-8, female human ES cell line H9 and human EC cell line NCCIT. *P value < 0.05, one sided t-test compared to control siRNA, n = 3 biological replicates. Error bars are ±1 s.d. e, RT–qPCR analysis of HERVK transcripts after siRNA knockdown of NANOG, OCT4 or SOX2 in human EC cells (NCCIT). Signals were normalized to 18S rRNA. *P value < 0.05, one sided t-test compared to control siRNA, n = 3 biological replicates. Error bars are ±1 s.d. f, ChIP-qPCR analyses of human ES cells (H9) with indicated antibodies. Signals were interrogated with primer sets for positive control regions (active human ES cell OCT4 and SOX2 enhancers), LTR5HS, or non-repetitive, intergenic negative regions, as indicated at the bottom. Shown is a representative result of two biological replicates.
a, Transcription factor knockdown in human EC cells (NCCIT). Cells were transfected with siRNA pools targeting indicated transcription factors and protein depletion was measured by immunofluoresence with respective antibodies in comparison with control, mock-transfected cells. DAPI (blue), OCT4 (green, left), NANOG (green, middle), SOX2 (green, right). Shown is one of three representative fields of view at ×20 magnification. b, Dual luciferase assays with indicated reporter constructs in human EC cells (NCCIT) showing that mutation of OCT4 site decreases reporter activity. N = 3 biological replicates, error-bars ±1 s.d. *P value < 0.05, one-sided t-test. SV40 enhancer/promoter construct was used as a positive control. c, Bisulfite sequencing for indicated cell types (WT33 human IPSC) analysing consensus LTR5HS-specific amplicon as in Fig. 2e. d, Bisulfite sequencing analysis of HERVK proviral consensus amplicon containing 3′ end of LTR, primer binding site, and 5′ region of Gag ORF (see Extended Data Fig. 2a) in indicated cell types: ELF1 naive, human ES cell, WT33 human IPSC, NCCIT human EC cell, or H9 human ES cell. e, RT–qPCR analysis of HERVK RNA levels in HEK293 cells treated with indicated concentrations of 5-aza-2′-deoxycytidine for 3 days, followed by transfection with OCT4/SOX2 expression constructs and RNA collection 48 h after transfection. qPCR primer sets were designed to three independent amplicons of HERVK. *P value < 0.05, one-sided t-test. n = 4 biological replicates, error bars ±1 s.d.
a, Immunofluorescence analysis of human EC cells (NCCIT) and human ES cells (H9) stained with DAPI (blue), OCT4 (green), Gag/Capsid (red), or IgG control (bottom). White boxes indicate regions shown in higher magnification/merge (right). Shown are representative fields of three independent experiments. b, Sensitivity of HERVK Gag/Capsid antibody immunoblot signal to HERVK knockdown. Human EC cells were transfected with one of three independent siRNA pools targeting HERVK Gag or with a control, non-targeting pool (synthesized against RFP) and total protein was analysed by immunoblotting with anti-Env and anti-Gag/Capsid antibodies. 1:2 serial dilution of total protein was loaded, as indicated. Blots were stripped and re-probed with TBP as a loading control. Shown is a representative result of two independent experiments. c, Sensitivity of HERVK Gag/Capsid antibody immunofluorescence signal to siRNA knockdown of Gag/Capsid (top) or control siRNA targeting RFP (bottom). Shown is a representative result of three fields of view. Magnification: 20X d, Immunoflourescence of naive ELF1 human ES cells with antibodies against OCT4 (green), HERVK Gag/Capsid (pink), DAPI in blue. Region marked with white box on left is shown with larger magnification (bottom). Magnification = 20x, 40x respectively. e, Another representative example of immunoflourescence of human blastocysts with DAPI (blue), OCT4 (green) and Gag/Capsid (red) shown (n = 19 blastocysts; DPF 5–6). Original magnification, ×40.
Extended Data Figure 5 TEM analyses of human EC cells and control embryo staining (supporting Fig. 3).
a, TEM analysis of human EC cells (NCCIT) with heavy metal staining; arrow indicates VLPs. Boxed region is shown with higher magnification in an inset. Scale bar = 500 nm. Shown is a representative example of two independent experiments. b, TEM immuno-gold labelling of human EC cells (NCCIT) with Gag/Capsid antibodies. Shown is a representative example from two independent experiments. c, Secondary antibody only control for immuno-gold labelling of human blastocysts. Shown is a representative example from eight fields of view. d, Model figure summarizing HERVK transcriptional regulation in human embryos and in vitro cultured pluripotent cells. Dashed lines indicate inference of OCT4, DNA methylation and HERVK level changes at implantation from those observed between naive and primed human ES cells, in the absence of data from actual postimplantation human embryos.
Extended Data Figure 6 Correlation of HERVK LTR5HS elements with gene expression (supporting Fig. 4).
a, Number of splice junctions identified linking indicated HERV class to annotated ReqSeq genes. Analysis was done using RNA-seq data set from ELF1 naive human ES cells, n = 3 biological replicates. b, Number of reads supporting chimaeric transcripts from indicated HERV class in ELF1 naive human ES cells, n = 3 biological replicates. c, Expression of LTR5HS linked genes plotted as a function of distance to the gene’s transcription start site (TSS). x-axis: distance of TSS to the nearest LTR5HS in kb; y-axis: fold change in expression of the linked gene in ELF1 naive versus primed human ES cells (this study, left) or expression of the linked gene in 3iL versus primed H1 human ES cells (right, ref. 12). d, Top, histograms showing expression of all genes that significantly change in expression between naive and primed ELF1 human ES cells (top histogram, white) or significantly changed genes that are LTR5HS associated (bottom histogram, blue); expression values from naive versus primed ELF1 human ES cell RNA-seq data sets (FDR < 0.05 DESeq). Fischer’s exact test gives stated P value, indicating enrichment of LTR5HS-linked genes in naive upregulated category. Bottom, quantification of average expression of LTR5HS-linked (blue) or unlinked (white) genes. Non-paired Wilcoxon test with stated P value indicating that genes linked to 1 or more LTR5HS have significantly higher mean expression. e, Top, histograms showing expression of all genes that significantly change in expression between 3iL and primed H1 human ES cells (top histogram, white) or significantly changed genes that are LTR5_HS associated (bottom histogram, blue); expression values from RNA-seq data sets reported previously12, FDR < 0.05 DESeq. Fischer’s exact test gives stated P value indicating enrichment of LTR5HS-linked genes in naive upregulated category. Bottom, quantification of average expression of LTR5HS-linked (blue) or unlinked (white) genes. Non-paired Wilcoxon test with stated P value indicating that genes linked to 1 or more LTR5HS have significantly higher mean expression.
Extended Data Figure 7 rec and IFITM1 expression in naive human ES cells, and effect of Rec expression on H1N1(PR8) infection (supporting Fig. 4).
a, Left, RT–qPCR analysis of HERVK rec expression levels in ELF1 naive human ES cells (n = 3 biological replicates) or H9 primed human ES cells (one biological replicate). Normalized to 18S rRNA. Right, Rec RNA levels in indicated blastocyst lineages. Solid line indicates mean; data are from ref. 10. b, RNA-seq quantification of IFITM1 RNA levels in naive or primed ELF1 human ES cells (left, this study) or 3iL human ES cells versus primed H1 human ES cells from ref. 12 (right). n = 3 biological replicates for each condition, error bars are ±1 s.d. Asterisk indicates significance at FDR < 0.05, DESeq. c, Flow cytometry for surface-localized IFITM1 staining in the indicated H9 human ES cells or naive ELF1 human ES cells (top) or, as a control for IFITM1 antibody specificity, knockdown of IFITM1 with two independent IFITM1 siRNA pools compared to control siRNA-treated cells in Flag–eGFP–Rec-hECCs (bottom). d, Left, IFITM1 expression in control human EC cell versus Rec-hECC (NCCIT) RNA-seq data sets. n = 2 biological replicates. Significance = FDR < 0.05, DESeq. Right, IFITM1 expression in control siRNA versus Rec siRNA-treated human EC cells (NCCIT) RNA-seq. n = 3 biological replicates, error bars are ±1 s.d. Significance = FDR < 0.05, DESeq. e, Flow-cytometry profiles for indicated cell types in H1N1(PR8) infected (top) or non-infected (bottom) wild-type (WT) control human EC cells or Flag–GFP–Rec-hECCs, clone #1. Shown is one representative example of four independent experiments showing a co-plating experiment in which GFP-Rec cells and wild-type control (GFP negative) cells are infected in the same well, stained in the same tube and identified by GFP fluorescence after gating for FSC and SSC. f, Scatterplot of ELF1 naive versus primed human ES cell RNA-seq showing all interferon-induced genes, with differentially regulated genes (FDR < 0.05 DESeq, n = 3 biological replicates each) highlighted in red. There is a significant overlap between differentially regulated genes and interferon-induced genes as measured by a hypergeometric test (P value < 0.05).
a, Diagram of iCLIP-seq procedure (see Methods for details). Briefly, cells are crosslinked using ultraviolet, lysed and digested with RNase to trim RNAs. Sequential immunopurification is performed using Flag M2, peptide elution, and GFP immunoprecipitation (IP). After stringent washing, RNAs are recovered and either radiolabelled (shown in b) or reverse transcribed and prepared for Illumina HTPS libraries. b, Autoradiogram of labelled RNAs (top) recovered from ultraviolet-crosslinked cells using sequential Flag–eGFP immunoprecipitation from: wild-type human EC cells (lanes 1, 2), Flag–eGFP control human EC cells (lanes 3, 4), or two independent Rec-hECC transgenic lines (lanes 5–8), separated on an SDS–polyacrylamide gel electrophoresis (SDS–PAGE) gel. Free Rec protein runs as a ∼35 kDa band, while Rec protein crosslinked to RNA molecules show lower electrophoretic mobility. Please note that: (1) Rec-bound RNAs are resistant to even high concentrations of RNaseI, probably indicating extensive secondary RNA structures, and (2) low/no background of contaminating RNAs in control immunoprecipitation from wild-type human EC cells or Flag–eGFP control human EC cells. Western blots with anti-GFP antibody were also performed to confirm the presence of tagged protein in Flag–eGFP control and Flag–eGFP–Rec cells, both in input and immunoprecipitation fractions (middle). HSP90 was used as a loading control (bottom). c, Computationally predicted (using mFold) secondary structure of LTR5HS sequence around the Rec response element (identified experimentally in vitro previously25). Single nucleotide resolution Rec ultraviolet-crosslinking sites determined by iCLIP are shaded in red; n = 2 biological replicates.
a, Genome browser representations of the Rec iCLIP read (n = 2 biological replicates) distribution at indicated mRNA targets. b, Computationally predicted (using mFold) secondary structures of indicated Rec iCLIP-seq targets. Single-nucleotide resolution Rec ultraviolet-crosslinking sites determined by iCLIP are shaded in red; to orient the reader, browser representation of the folded fragment is shown above each respective cartoon.
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Grow, E., Flynn, R., Chavez, S. et al. Intrinsic retroviral reactivation in human preimplantation embryos and pluripotent cells. Nature 522, 221–225 (2015). https://doi.org/10.1038/nature14308
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