PUBLICATION

Developmental expression of the alpha-skeletal actin gene

Authors
Bertola, L.D., Ott, E.B., Griepsma, S., Vonk F.J., Bagowski, C.P.
ID
ZDB-PUB-221207-9
Date
2008
Source
BMC Evolutionary Biology   8: 166 (Journal)
Registered Authors
Ott, Elisabeth B.
Keywords
none
MeSH Terms
  • Actins/chemistry
  • Actins/genetics*
  • Amino Acid Sequence
  • Animals
  • Gene Expression Regulation, Developmental*
  • In Situ Hybridization
  • Mice
  • Models, Molecular
  • Molecular Sequence Data
  • Muscle, Skeletal/embryology
  • Phylogeny
  • Sequence Alignment
  • Zebrafish
PubMed
18518953 Full text @ BMC Evol. Biol.
Abstract
Background: Actin is a cytoskeletal protein which exerts a broad range of functions in almost all eukaryotic cells. In higher vertebrates, six primary actin isoforms can be distinguished: alpha-skeletal, alpha-cardiac, alpha-smooth muscle, gamma-smooth muscle, beta-cytoplasmic and gamma-cytoplasmic isoactin. Expression of these actin isoforms during vertebrate development is highly regulated in a temporal and tissue-specific manner, but the mechanisms and the specific differences are currently not well understood. All members of the actin multigene family are highly conserved, suggesting that there is a high selective pressure on these proteins. Results: We present here a model for the evolution of the genomic organization of alpha-skeletal actin and by molecular modeling, illustrate the structural differences of actin proteins of different phyla. We further describe and compare alpha-skeletal actin expression in two developmental stages of five vertebrate species (mouse, chicken, snake, salamander and fish). Our findings confirm that alpha-skeletal actin is expressed in skeletal muscle and in the heart of all five species. In addition, we identify many novel non-muscular expression domains including several in the central nervous system. Conclusion: Our results show that the high sequence homology of alpha-skeletal actins is reflected by similarities of their 3 dimensional protein structures, as well as by conserved gene expression patterns during vertebrate development. Nonetheless, we find here important differences in 3D structures, in gene architectures and identify novel expression domains for this structural and functional important gene.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping