Nucleotide- and Protein-Dependent Functions of Actg1

Cytoplasmic β- and γ-actin proteins are 99% identical but support unique organismal functions. The cytoplasmic actin nucleotide sequences   and  , respectively, are more divergent but still 89% similar.  mice are embryonic lethal and  cells fail to proliferate, but editing the   gene to express γ-ac...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular biology of the cell 2022-08, Vol.33 (9), p.ar77-ar77
Hauptverfasser: Sundby, Lauren J, Southern, William M, Hawbaker, Katelin M, Trujillo, Jesús M, Perrin, Benjamin J, Ervasti, James M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Cytoplasmic β- and γ-actin proteins are 99% identical but support unique organismal functions. The cytoplasmic actin nucleotide sequences   and  , respectively, are more divergent but still 89% similar.  mice are embryonic lethal and  cells fail to proliferate, but editing the   gene to express γ-actin ( ) resulted in none of the overt phenotypes of the knockout revealing protein-independent functions for  . To determine if  has a protein-independent function, we crossed   and  mice to generate the bG/0 line, where the only cytoplasmic actin expressed is γ-actin from  . The bG/0 mice were viable but showed a survival defect despite expressing γ-actin protein at levels no different from bG/gG with normal survival. A unique myopathy phenotype was also observed in bG/0 mice. We conclude that impaired survival and myopathy in bG/0 mice are due to loss of   nucleotide-dependent function(s). On the other hand, the bG/0 genotype rescued functions impaired by  , including cell proliferation and auditory function, suggesting a role for γ-actin protein in both fibroblasts and hearing. Together, these results identify nucleotide-dependent functions for   while implicating γ-actin protein in more cell-/tissue-specific functions.
ISSN:1059-1524
1939-4586
DOI:10.1091/mbc.E22-02-0054