Cargando…
Functional mechanisms of MYRF DNA-binding domain mutations implicated in birth defects
Myrf is a pleiotropic membrane-bound transcription factor that plays critical roles in diverse organisms, including in oligodendrocyte differentiation, embryonic development, molting, and synaptic plasticity. Upon autolytic cleavage, the Myrf N-terminal fragment enters the nucleus as a homo-trimer a...
Autores principales: | Fan, Chuandong, An, Hongjoo, Sharif, Mohamed, Kim, Dongkyeong, Park, Yungki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094900/ https://www.ncbi.nlm.nih.gov/pubmed/33798553 http://dx.doi.org/10.1016/j.jbc.2021.100612 |
Ejemplares similares
-
Functional mechanism and pathogenic potential of MYRF ICA domain mutations implicated in birth defects
por: An, Hongjoo, et al.
Publicado: (2020) -
Elucidating the transactivation domain of the pleiotropic transcription factor Myrf
por: Choi, Jin-ok, et al.
Publicado: (2018) -
Homo-trimerization is essential for the transcription factor function of Myrf for oligodendrocyte differentiation
por: Kim, Dongkyeong, et al.
Publicado: (2017) -
Identifying an oligodendrocyte enhancer that regulates Olig2 expression
por: Fan, Chuandong, et al.
Publicado: (2022) -
Uncovering oligodendrocyte enhancers that control Cnp expression
por: Fan, Chuandong, et al.
Publicado: (2023)