Molecular mechanisms underlying formin-associated inherited deafness - Molecular mechanisms underlying formin-associated inherited deafness
Summary
This R15 AREA proposal will support investigations of the molecular mechanisms by which
cytoskeletal structures in the inner ear are built and maintained. Mutations of the human
Diaphanous 1 (DIAPH1) gene causes autosomal dominant, non-syndromic, progressive hearing
loss, referred to as DFNA1. The molecular mechanisms underlying this form of deafness are
unknown. DFNA1 could serve as a model for inner ear maintenance over a lifetime. DIAPH1 is
a member of the formin family of actin and microtubule cytoskeletal regulators. The inner ear
contains several precisely constructed cytoskeletal structures, most notably the bundle of
stereocilia on hair cells. Investigations of deafness-associated cytoskeletal regulators will
contribute to our understanding of biology of the inner ear. This project will use DFNA1
mutations as a starting point for understanding the role of formins in the inner ear. The proposed
work will test three related hypotheses: (1) that the deafness-associated mutations in DFNA1
disrupt the protein's intramolecular regulatory interaction, (2) that the mutations compromise the
ability of DIAPH1 to regulate the assembly of actin filaments, and (3) that the same mutant
proteins are compromised in their ability to collaborate with other actin regulatory proteins that
are highly expressed in the hair cells of the inner ear. All three hypotheses are plausible given
that the locations of several DFNA1 mutations coincide with a domain that interacts with
cytoskeletal filaments, intramolecular regulatory domains, and other cytoskeletal regulatory
proteins. To test these hypotheses, a set of reductionist biochemistry experiments are
proposed, including protein:protein interaction and actin filament assembly assays. These
experiments are accessible for undergraduate researchers, and the overarching research
questions will be of interest to students pursuing careers in the biomedical sciences.