Cargando…
N-terminal sequences in Matrin 3 mediate phase separation into droplet-like structures that recruit TDP43 variants lacking RNA binding elements
RNA binding proteins associated with amyotrophic lateral sclerosis (ALS) and muscle myopathy possess sequence elements that are low in complexity, or bear resemblance to yeast prion domains. These sequence elements appear to mediate phase separation into liquid-like membraneless organelles. Using fu...
Autores principales: | Gallego-Iradi, M. Carolina, Strunk, Haley, Crown, Anthony M., Davila, Rachel, Brown, Hilda, Rodriguez-Lebron, Edgardo, Borchelt, David R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857798/ https://www.ncbi.nlm.nih.gov/pubmed/31019288 http://dx.doi.org/10.1038/s41374-019-0260-7 |
Ejemplares similares
-
Characterization of gene regulation and protein interaction networks for Matrin 3 encoding mutations linked to amyotrophic lateral sclerosis and myopathy
por: Iradi, M. Carolina Gallego, et al.
Publicado: (2018) -
Subcellular Localization of Matrin 3 Containing Mutations Associated with ALS and Distal Myopathy
por: Gallego-Iradi, M. Carolina, et al.
Publicado: (2015) -
Translational regulation in the brain by TDP-43 phase separation
por: Gao, Ju, et al.
Publicado: (2021) -
Watching liquid droplets of TDP-43(CTD) age by Raman spectroscopy
por: Shuster, Sydney O., et al.
Publicado: (2021) -
Phase separation-deficient TDP43 remains functional in splicing
por: Schmidt, Hermann Broder, et al.
Publicado: (2019)