Abstract:
Axonal branching process is an essential mechanism for forming complex neural
circuits by facilitating in the formation of multiple synaptic connections with multiple
target-fields. Even though the axonal branching mechanism is still poorly understood,
several potential candidates might have a role in the axonal branching process, but our
attention went to FMN2 protein due to its increased expression level in the nervous
system of mammals and few studies implicating FMN2 with intellectual disabilities.
FMN2 is actin nucleation and elongation protein from a well-known Protein family called
Formins. There are studies confirming FMN2 being an actin bundling and microtubule
interacting protein. These diverse functions with the cytoskeletal system found to be
useful in an axonal branching process. From this project, actin nucleation and
elongation activity of FMN2 was found to be regulating the protrusive activity. The actin
patch majorly governs initiation of a protrusion and FMN2 was found to be influencing
actin patch dynamics also. Depletion of FMN2 in neurons significantly reduced the
lifetime and area of actin patch in the axon shaft and by overexpressing the FMN2 in
neurons displayed a distinguishable increase in actin patch lifetime. Still, there is a lot to
be understood about axonal branching mechanism from the perspective of FMN2.
Hence this project is going ahead in search of that.
