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Published on: March 17, 2011
Cytoskeletal actin genes function downstream of HNF-3beta in ascidian notochord development
W R Jeffery1, N Ewing, J Machula
1Department of Biology, Pennsylvania State University, University Park 16802, USA. wrj1@psu.edu
Abstract:
We have examined the expression and regulation of cytoskeletal actin genes in ascidians with tailed (Molgula oculata) and tailless larvae (Molgula occulta). Four cDNA clones were isolated representing two pairs of orthologous cytoskeletal actin genes (CA1 and CA2), which encode proteins differing by five amino acids in the tailed and tailless species. The CA1 and CA2 genes are present in one or two copies, although several related genes may also be present in both species. Maternal CA1 and CA2 mRNA is present in small oocytes but transcript levels later decline, suggesting a role in early oogenesis. In the tailed species, embryonic CA1 and CA2 mRNAs first appear in the presumptive mesenchyme and muscle cells during gastrulation, subsequently accumulate in the presumptive notochord cells, and can be detected in these tissues through the tadpole stage. CA1 mRNAs accumulate initially in the same tissues in the tailless species but subsequently disappear, in concert with the arrest of notochord and tail development. In contrast, CA2 mRNAs were not detected in embryos of the tailless species. Fertilization of eggs of the tailless species with sperm of the tailed species, which restores the notochord and the tail, also results in the upregulation of CA1 and CA2 gene expression in hybrid embryos. Antisense oligodeoxynucleotide experiments suggest that CA1 and CA2 expression in the notochord, but not in the muscle cells, is dependent on prior expression of Mocc FHI, an ascidian HNF-3beta-like gene. The expression of the CA1 and CA2 genes in the notochord in the tailed species, downregulation in the tailless species, upregulation in interspecific hybrids, and dependence on HNF-3beta activity is consistent with a role of these genes in development of the ascidian notochord.
Insights
Cytoskeletal actin genes (CA1 and CA2) play a crucial role in ascidian notochord development. Their expression patterns, particularly in tailed versus tailless larvae, highlight their importance in developmental regulation.
Area of Science:
- Developmental Biology
- Genetics
- Molecular Biology
Background:
- Cytoskeletal actin genes are essential for cellular structure and function.
- Ascidian larvae exhibit variations in development, including the presence or absence of a tail, offering a model for studying developmental gene regulation.
Purpose of the Study:
- To investigate the expression and regulation of cytoskeletal actin genes (CA1 and CA2) in ascidians with tailed and tailless larvae.
- To determine the role of these actin genes in embryonic development, specifically in notochord and tail formation.
Main Methods:
- Isolation and characterization of cytoskeletal actin gene cDNA clones (CA1 and CA2).
- Analysis of gene expression patterns using mRNA detection in different developmental stages and larval types.
- Interspecific hybridization experiments and antisense oligodeoxynucleotide studies to assess gene function and regulation.
Main Results:
- Two pairs of orthologous cytoskeletal actin genes (CA1 and CA2) were identified, encoding proteins with minor differences between species.
- Maternal CA1 and CA2 mRNA are present in early oocytes but decline later.
- In tailed ascidians, CA1 and CA2 are expressed in mesenchyme, muscle, and notochord cells. In tailless ascidians, CA1 expression is transient, and CA2 is not detected.
- Interspecific hybrids show restored notochord/tail development and upregulated CA1/CA2 expression.
- CA1 and CA2 notochord expression depends on Mocc FHI (an HNF-3beta-like gene).
Conclusions:
- CA1 and CA2 genes are critical for ascidian notochord development.
- Differential expression of CA1 and CA2 is linked to the presence or absence of a tail and notochord formation.
- The regulation of CA1 and CA2 expression involves factors like Mocc FHI, underscoring their role in developmental pathways.
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