Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Oct 4;220(10):e202102146.
doi: 10.1083/jcb.202102146. Epub 2021 Aug 30.

The cell biology of fertilization: Gamete attachment and fusion

Affiliations
Review

The cell biology of fertilization: Gamete attachment and fusion

Karen K Siu et al. J Cell Biol. .

Abstract

Fertilization is defined as the union of two gametes. During fertilization, sperm and egg fuse to form a diploid zygote to initiate prenatal development. In mammals, fertilization involves multiple ordered steps, including the acrosome reaction, zona pellucida penetration, sperm-egg attachment, and membrane fusion. Given the success of in vitro fertilization, one would think that the mechanisms of fertilization are understood; however, the precise details for many of the steps in fertilization remain a mystery. Recent studies using genetic knockout mouse models and structural biology are providing valuable insight into the molecular basis of sperm-egg attachment and fusion. Here, we review the cell biology of fertilization, specifically summarizing data from recent structural and functional studies that provide insights into the interactions involved in human gamete attachment and fusion.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Gametogenesis and fertilization. (A–C) Illustration of oogenesis and follicle development (A), spermatogenesis (B), and the major steps in fertilization (C): (1) initial contact, (2) acrosome reaction, (3) ZP penetration, (4) sperm–egg fusion, (5) entry of sperm nucleus, (6) cortical reaction, and (7) fusion of the sperm and egg nuclei. The oocyte with its ZP measures 130 μm in diameter. Created with BioRender.
Figure 2.
Figure 2.
Structures of cellular factors involved in sperm–egg attachment and fusion. (A) Human IZUMO1 is shaped like a boomerang in an unbound state (Protein Data Bank [PDB] accession no. 5F4T). The 4HB, hinge, and IgSF domains are shown in orange, green, and cyan, respectively. (B) Human JUNO (PDB accession no. 5F4Q) belongs to the folate receptor family. (C) The structure of human IZUMO1–JUNO complex (PDB accession no. 5F4E) reveals that JUNO binds to IZUMO1 via the β-hairpin hinge, four residues from the 4HB domain and two from the IgSF domain. (D) Human CD9 (PDB accession no. 6K4J) adopts a conical shape formed by four transmembrane helices (TM1–TM4; blue) and two extracellular loops (SEL, pink; and LEL, red).
Figure 3.
Figure 3.
Current model of sperm–egg attachment and fusion. (A) Acrosome reaction. After the acrosome reaction, IZUMO1 (blue), SPACA6 (purple), and TMEM95 (violet) colocalize to the equatorial regions of sperm. FIMP (pink) appears to function before the acrosome reaction. There are conflicting data on whether or not TMEM95 interacts with IZUMO1. SOF1 (turquoise) is a secreted sperm protein. DCST1 (green) and DCST2 (orange) are transmembrane proteins implicated in regulating the protein stability of SPACA6. (B) Initial attachment. After the sperm reaches the PVS, it attaches to the egg. IZUMO1 is localized on the equatorial segment of acrosome-reacted sperm and its counterpart receptor, JUNO (yellow), on the oocyte membrane. JUNO specifically recognizes and binds to IZUMO1 in a monomeric conformation. IZUMO1 binding to JUNO drives the accumulation of CD9 (pink) at the sperm–egg interface to form a physical anchor that holds the sperm and oocyte membranes in proximity. (C) IZUMO1 multimerization. After the initial IZUMO1–JUNO attachment, the complex undergoes a dimerization event. The trigger for IZUMO1 oligomerization is not fully understood; however, colocalization analysis revealed the presence of PDI (gray) on the sperm surface. JUNO is thought to be shed from the oolemma and into the PVS after fertilization. (D) Fusogen recruitment. The bona fide sperm–egg fusogen remains a mystery. However, data suggest that IZUMO1 forms a scaffold to recruit the gamete fusion complex. The roles of SPACA6, TMEM95, and SOF1 remain unclear, but these proteins likely play roles in fusion. (E) Fusion pore formation. The merger of the egg and sperm membranes requires modulation of the membrane architecture. The fusogen is thought to catalyze the formation of a hemifusion intermediate, which is a stalk-like structure where the outer leaflets of the sperm and egg membrane bilayers mix. Subsequently, the inner bilayer leaflets mix to form the fusion pore. The precise mechanism of this step will require the identification of the sperm–egg fusogen. Created with BioRender.

Similar articles

Cited by

References

    1. Aitken, R.J., Baker M.A., Doncel G.F., Matzuk M.M., Mauck C.K., and Harper M.J.K.. 2008. As the world grows: contraception in the 21st century. J. Clin. Invest. 118:1330–1343. 10.1172/JCI33873 - DOI - PMC - PubMed
    1. Atwood, C.S., and Vadakkadath Meethal S.. 2016. The spatiotemporal hormonal orchestration of human folliculogenesis, early embryogenesis and blastocyst implantation. Mol. Cell. Endocrinol. 430:33–48. 10.1016/j.mce.2016.03.039 - DOI - PubMed
    1. Austin, C.R. 1952. The capacitation of the mammalian sperm. Nature. 170:326. 10.1038/170326a0 - DOI - PubMed
    1. Aydin, H., Sultana A., Li S., Thavalingam A., and Lee J.E.. 2016. Molecular architecture of the human sperm IZUMO1 and egg JUNO fertilization complex. Nature. 534:562–565. 10.1038/nature18595 - DOI - PMC - PubMed
    1. Barbaux, S., Ialy-Radio C., Chalbi M., Dybal E., Homps-Legrand M., Do Cruzeiro M., Vaiman D., Wolf J.-P., and Ziyyat A.. 2020. Sperm SPACA6 protein is required for mammalian Sperm-Egg Adhesion/Fusion. Sci. Rep. 10:5335. 10.1038/s41598-020-62091-y - DOI - PMC - PubMed

Publication types