Yuna Ayala, Ph.D., Assistant Professor of Biochemistry, published a paper in The Journal of Biological Chemistry detailing studies on TAR DNA-ginding Protein 43 (TDP-43) and its role in neurodegenerative diseases, such as amytrophic lateral sclerosis (ALS).

TDP-43 regulates gene expression through RNA processing, and is essential for development and survival. It also forms intracellular aggregates in ALS and some other neurological diseases, resulting in loss of function of normal TDP-43. The researchers found that double phosphorylation of TDP-43 by MEK, a kinase in the MAPK/ERK signaling pathway that is activated by cellular heat shock response (HSR), did not aggregate and showed decreased splicing activity. These results uncovered a previously unknown mechanism of regulation for TDP-43, which could lead to new strategies to treat aggregation as well as new roles of TDP-43 in cellular metabolism.

For more information, read the full article in Newslink.