| First Author | Hook J | Year | 2011 |
| Journal | Bioarchitecture | Volume | 1 |
| Issue | 1 | Pages | 49-59 |
| PubMed ID | 21866263 | Mgi Jnum | J:280466 |
| Mgi Id | MGI:6368347 | Doi | 10.4161/bioa.1.1.15172 |
| Citation | Hook J, et al. (2011) Functional identity of the gamma tropomyosin gene: Implications for embryonic development, reproduction and cell viability. Bioarchitecture 1(1):49-59 |
| abstractText | The actin filament system is fundamental to cellular functions including regulation of shape, motility, cytokinesis, intracellular trafficking and tissue organization. Tropomyosins (Tm) are highly conserved components of actin filaments which differentially regulate filament stability and function. The mammalian Tm family consists of four genes; alphaTm, betaTm, gammaTm and deltaTm. Multiple Tm isoforms (>40) are generated by alternative splicing and expression of these isoforms is highly regulated during development. In order to further identify the role of Tm isoforms during development, we tested the specificity of function of products from the gammaTm gene family in mice using a series of gene knockouts. Ablation of all gammaTm gene cytoskeletal products results in embryonic lethality. Elimination of just two cytoskeletal products from the gammaTm gene (NM1,2) resulted in a 50% reduction in embryo viability. It was also not possible to generate homozygous knockout ES cells for the targets which eliminated or reduced embryo viability in mice. In contrast, homozygous knockout ES cells were generated for a different set of isoforms (NM3,5,6,8,9,11) which were not required for embryogenesis. We also observed that males hemizygous for the knockout of all cytoskeletal products from the gammaTm gene preferentially transmitted the minus allele with 80-100% transmission. Since all four Tm genes are expressed in early embryos, ES cells and sperm, we conclude that isoforms of the gammaTm gene are functionally unique in their role in embryogenesis, ES cell viability and sperm function. |
