DST research on role of proteins in neuronal development to inspire new treatment protocols
02 August 2021
Priyanka Dutta, an Inspire Faculty Fellow, has recently uncovered the mechanism by which a protein called Formin-2 disrupts neural connectivity and could result in developmental defects associated with intellectual disability and deficits in learning and memory.
Establishment of a functional neuronal circuit is essential for proper functioning of the nervous system. To understand the neuronal coordination of an organism, it is important to comprehend how the underlying cytoskeleton or the complex network of interlinking protein filaments in the cytoplasm of cells assemble and function assisted by its regulatory proteins. The errors in neuronal connectivity are central to genetic mutations of these proteins, which lead to detrimental developmental defects.
Priyanka Dutta from the National Centre for Cell Science, Pune, a recipient of the Inspire Faculty fellowship instituted by the Department of Science & Technology, focuses on understanding the mechanical function of the cytoskeletal proteins involved in neuro-developmental disorder. This understanding of neurobiological mechanism of the disorder can help to modify the treatment protocol to minimise the symptoms of the disease.
Her recent study has tracked the role of Formin-2 in regulating how the microtubules or actin filaments in the cytoskeleton that are responsible for cellular reorganisation and chromosome separation dynamically organise themselves. The team has identified that Formin-2 cross-links actin-microtubule to form polymers in neurons with the help of its C-terminal FSI tail. This mechanism might have important implications for understanding underlying neuro-developmental conditions, such as intellectual disability, that have been linked to mutations in Formin-2.
This research has been published in the ‘Journal of Cell Science’.
Priyanka Dutta said her proposed project involves understanding the regulatory roles of Formin-2 in neuronal development. The output from this project will be a bedrock for prospective research, which will explore how cytoskeleton regulators communicate with other signaling molecules along with actin and microtubule to distinguish between the normal and abnormal states before the onset of neuronal diseases.