The process is therefore tightly regulated. Specialized proteins
called “fusogens” must be present at the precise time and place to allow
the egg and the sperm to merge into one.
The Podbilewicz lab studies fusogens in several organisms. It first
identified and characterized two such proteins in the nematode C.
elegans (EFF-1 and AFF-1) worms, which are about a millimeter long with
959 somatic cells. Its transparent body consists of three layers: an
epidermal layer, an intestinal layer and a muscle layer.
These proteins are involved in organ development but not in
fertilization. Surprisingly, the structural analysis revealed that these
proteins have a very similar three-dimensional structure to another
fusogen involved in fertilization in plants (GCS1/HAP2).
This family of similarly structured fusion proteins has been named
fusexins. It includes representatives in plants, animals, viruses,
unicellular algae and parasites.
Connecting the familial dots
To expand upon and characterize
the origin and evolution of the Fusexin family, research collaborator
David Moi and a team of researchers from Argentina and Switzerland
conducted a bioinformatic search on genetic sequences sampled from
different environments. After screening samples from soil, saline lakes,
freshwater, and marine sediments, they discovered 96 sequences
belonging to archaea, which showed some similarities with known fusion
proteins.
The sequences were named fusexin1 (Fsx1), and an expert team led by
Pablo Aguilar, Hector Romero and Martin Graña in Uruguay and Argentina
confirmed that they belong to archaea species from lineages estimated to
originate 3 billion years ago; however, it remained unclear whether the
protein that Fsx1 encodes looks similar to members of the fusexin
family and whether it is truly capable of mediating cell-to-cell fusion.
What's the next step?
To determine the structure of an Fsx1 protein, Shunsuke Nishio of the Karolinska Institute in Sweden used crystallographic methods to decipher the three-dimensional conformation of the Fsx1 protein.
Nishio showed that the Fsx1 protein contains three structural domains
very similar to known Fusexin members and is arranged in a three-piece
complex – known as a trimer – as do other known fusogens. Surprisingly,
Fsx1 has an additional fourth domain not found in any known Fusexin
member. Prof. Luca Jovine, leading the crystallographic structure
analysis, also used novel machine-learning software (AlphaFold2) to
determine the structure of the Fsx1 protein.
To prove that the protein Fsx1 carries a fusogen role, doctoral
student Xiaohui Li from the Podbilewicz Laboratory conducted an
experiment in which she expressed the Fsx1 protein in a cell culture
derived from mammals, which typically do not fuse. In collaboration with
lab manager Clari Valansi and lab members Dr. Nicolas Brukman and
Kateryna Flyak, Li showed that Fsx1 from archaea does induce the fusion
of these mammalian cells that diverged one to two billion years ago.
Known Fusexin proteins in viruses serve to mediate viral entry into the host cell (as is the case for coronavirus),
while in eukaryotes (cells with nuclei) – plants, nematodes, and
protists – they play roles in organ sculpting, neuronal repair and sex.
But who came first? Was a fusogen used for sexual reproduction
snatched by a virus, or was a viral protein used for infection adopted
by plants?
The study by Moi, Nishio, Li and others raises a possible third scenario: all
fusexins originate in archaea, from which the lineage split into a
variety of functions, from viral infection to sperm and egg fusion – a
billion years before sexual reproduction.
Where does this leave us?
An important next step will be to study what Fsx1 proteins are doing
in nature. Do they fuse archaeal cells like their plant and animal
fusexins counterparts fuse gametes (eggs and sperm) to promote a
sex-like DNA exchange?
Parallel studies will also be needed to understand the evolutionary
history connecting the Fsx1 protein and GCS1/HAP2 in order to establish
what their origin is. Archaeal fusexins and other still undiscovered
fusogens might help us to understand how cells evolved from apparently
simple forms sharing discrete pieces of DNA between them to today’s
complex life forms undergoing sexual reproduction.
Thus,
the discovery that ancient creatures like archaea can also contain
fusexin proteins now raises the intriguing possibility whereby the Fsx1
protein is the ancestral version from which viral, plant, and animal
fusogens derived.
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