Figures and data
Mouse sperm do not bind to zebrafish zona proteins.
A) Schematic of zebrafish ZP2 and ZP3 peptides compared to mammalian homologs (Clustal Ω). Yellow bars represent cysteine residues. Percent values indicate identity between mouse and zebrafish amino acid sequences (NP_035905.1, mouse ZP2; AAK16578.1, zebrafish ZP2, variant A; AAK16577.1, zebrafish ZP2, variant B; AAK16579.1, zebrafish ZP2, variant C; NP_035906.1, mouse ZP3; NP_571406, zebrafish ZP3). B) SDS-PAGE of recombinant zebrafish ZP2, ZP3, or ZP2 and ZP3 peptides (6-His mAb, immunoblot) expressed in Sf9 cells after purification from agarose beads. Molecular mass is indicated on the left. C) Capacitated mouse sperm binding to beads carrying zebrafish (zf) ZP2, zfZP3 or zebrafish zfZP2 and zfZP3. Beads carrying mouse (m) ZP2 N-termini and beads alone were used as positive and negative controls, respectively. Differential Interference Contrast (DIC) (top) and confocal z projection (bottom) images, sperm nuclei (blue) stained with Hoechst. D) Boxplots represent the median (vertical line) number of mouse sperm binding to mammalian/fish peptide beads or beads alone and data points within the 10th and 90th percentiles (error bars). Boxes include the middle two quartiles, and dots indicate the outliers. Superscript letters show statistical significance (P<0.05) defined by One-Way ANOVA followed by Tukey HSD (honestly significant difference) post-hoc test. E) Schematic of cross-species insemination assays using mouse sperm to inseminate zebrafish chorion (Top) or eggs (Bottom). F) Representative pictures of zebrafish chorion or eggs inseminated with mouse sperm; Top-right panel: mouse sperm binding to normal mouse eggs after 60 min of incubation. Inset, 2.0× magnification. Mouse two-cell embryos serve as a negative control for sperm binding. Bottom-right panel: mouse sperm binding to mouse two-cell embryos; mouse eggs serve as an internal positive control for mouse sperm binding. Top-left panel: mouse sperm incubated with zebrafish chorion without ovulated oocyte (60 min incubation). Bottom-left panel: mouse sperm incubated with zebrafish ovulated oocytes (60 min incubation). G) Boxplots represent the median (vertical line) number of mouse sperm binding to mammalian/fish oocytes or embryos (sperm bound per 20 µm2 projected surface area) and data points within the 10th and 90th percentiles (error bars). Boxes include the middle two quartiles, and dots indicate the outliers. Superscript letters show statistical significance (P<0.05) defined by One-Way ANOVA followed by Tukey HSD (honestly significant difference) post-hoc test.
Fish sperm interaction with the micropyle.
A) Confocal images of the micropyle stained by WGA-633 in zebrafish oocytes (n >15); arrows indicate the micropyle. B) Zebrafish in vitro insemination: Hoechst-stained zebrafish sperm (light blue) that have approached or entered the micropyle in freshly ovulated oocytes (yellow, WGA-633-stained); samples were fixed in paraformaldehyde few seconds after insemination. C) Zebrafish eggs untreated (left) or treated with trypsin to eliminate the micropyle protein (right). D) Fluorescence was measured (Fiji/ImageJ) within a 20 µm2 area; 0 indicates the micropyle opening position (yellow), 160 µm indicates the most distant position measured from micropyle opening. E) Same as in (C); left, DIC, right, confocal images (maximum intensity projection) of zebrafish oocytes inseminated with zebrafish sperm. F) Same as in 1G, for the quantification of the number of zebrafish sperm approaching and entering the micropyle of oocytes treated/not treated (control) with trypsin (n = 3). G) Same as in 1G, for fertilization rates (n = 3).
Mouse sperm cross the fish micropyle.
A) Cross-species insemination: mouse sperm (Hoechst-stained, light blue) in the zebrafish micropyle region of a chorion (60 min incubation) surrounding the oocyte (left), or of a chorion mechanically freed from the oocyte (right, Ghost). B) Quantification of mouse sperm in the micropyle region of chorion with or without zebrafish oocyte: same as 1G; mouse eggs or two-cell embryos served as an internal positive and negative control for sperm binding (n = 3). C) X-Y plane confocal projection of zebrafish chorion encompassing the WGA-633 (yellow) micropyle region (∼320 µm); bar with arrows indicates positions at which fluorescence was measured (Fiji/ImageJ) as in 2D. D) Quantification of mouse sperm across the micropyle region: boxplots represent the median (vertical line) raw integrated density ratio (RID ratio, left Y axis) measured on ten zebrafish VEs; data points within the 10th and 90th percentiles (error bars). Boxes include the middle two quartiles, and dots indicate the outliers. A light blue line represents the number of sperm (right Y axis) found in the corresponding chorion position (X axis); error bars represent s.e.m.; statistical significance (P<0.05) across RID ratios or sperm numbers in different positions is defined by One-Way ANOVA followed by Tukey HSD post-hoc test. E) Time-lapse frames from supplementary video 1, showing the first sperm entering the micropyle of a freshly ovulated zebrafish egg. Green arrowheads indicate mouse sperm. Insets show the number of seconds (‘s’) after the first sperm appears in the field of view.
Localization and dynamics of sperm interactions with the micropyle and inter-chorion space in zebrafish oocytes.
A) Hoechst-stained sperm (blue) which has crossed the micropyle. DIC (left) and confocal (mid-panel) projection of sperm accumulated in the inter-chorion space (ICS) of a zebrafish oocyte imaged from the top; in the left- and middle/top panels, the 633 channel is turned off to visualize the sperm accumulated in the ICS around the micropyle region (yellow circled); inset shows a longitudinal section of the same oocyte, showing the Hoechst-stained sperm (blue) under the WGA-633-stained micropyle region (yellow). Right, Hoechst-stained sperm (blue) is included in the PVS. B) Quantification as in 1D of mouse sperm in the ICS below (left) or away (right) from the micropyle region. Error bars represent s.e.m., statistical significance (P<0.05) is defined by One-Way ANOVA followed by Tukey HSD. C) Electron microscopy of mouse sperm in the zebrafish micropyle region and within the micropyle canal, 1 hour after insemination. Left, SEM, mid and right panels, TEM; IAM, inner acrosomal membrane. OAM, outer acrosomal membrane; ES, equatorial segment. D) AcrTg sperm in the micropyle region. Left, DIC, right, confocal projection. The yellow arrow indicates the micropyle opening. E) As in 1G, with AcrTg sperm (intact vs. reacted). F) Acrosome-intact (red arrows) and reacted (light-blue arrows) mouse sperm in zebrafish ICS. Inset represents a 2x magnification of an acrosome-intact sperm in the ICS.
CatSper is necessary for mouse sperm crossing the zebrafish micropyle.
A) Hoechst-stained fertile Catsper1Het (Normal, left) and Catsper1Null sperm binding to ovulated mouse eggs. B) Same as in 1D, per mouse egg. C) Fertile Catsper1Het (Normal, left) and Catsper1Null sperm in the PVS of Cd9Nullfemale eggs upon in vivo mating. D) Same as in 1D, number of PVS sperm per Cd9Null mouse egg. E) Fertile Catsper1Het (Normal, left) and Catsper1Null (right) Hoechst-stained sperm in the micropyle region of zebrafish eggs; top, DIC image, bottom, confocal. F) Same as in 1G, with normal vs. Catsper1Nullsperm.
Zebrafish eggs in HTF/HSA.
Zebrafish eggs maintained either in Hank’s solution at room temperature (top) or under mouse IVF conditions (bottom) for 240 min.
Trypsin treatment of zebrafish micropyle.
A) Zebrafish eggs untreated (left) or treated with trypsin to eliminate the MP (right); top panels, DIC images, bottom panel, confocal images. Yellow is the MP stained with WGA-633. B) Same as in 1G, with zebrafish trypsin-treated vs. untreated.
