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Published on: January 26, 2013
The midblastula transition defines the onset of Y RNA-dependent DNA replication in Xenopus laevis
Clara Collart1, Christo P Christov, James C Smith
1Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, United Kingdom.
Abstract:
Noncoding Y RNAs are essential for the initiation of chromosomal DNA replication in mammalian cell extracts, but their role in this process during early vertebrate development is unknown. Here, we use antisense morpholino nucleotides (MOs) to investigate Y RNA function in Xenopus laevis and zebrafish embryos. We show that embryos in which Y RNA function is inhibited by MOs develop normally until the midblastula transition (MBT) but then fail to replicate their DNA and die before gastrulation. Consistent with this observation, Y RNA function is not required for DNA replication in Xenopus egg extracts but is required for replication in a post-MBT cell line. Y RNAs do not bind chromatin in karyomeres before MBT, but they associate with interphase nuclei after MBT in an origin recognition complex (ORC)-dependent manner. Y RNA-specific MOs inhibit the association of Y RNAs with ORC, Cdt1, and HMGA1a proteins, suggesting that these molecular associations are essential for Y RNA function in DNA replication. The MBT is thus a transition point between Y RNA-independent and Y RNA-dependent control of vertebrate DNA replication. Our data suggest that in vertebrates Y RNAs function as a developmentally regulated layer of control over the evolutionarily conserved eukaryotic DNA replication machinery.
Insights
Noncoding Y RNAs are crucial for DNA replication initiation in vertebrates. Their function becomes essential after the midblastula transition (MBT), regulating replication in developing embryos.
Area of Science:
- Developmental Biology
- Molecular Biology
- Genetics
Background:
- Noncoding Y RNAs are vital for DNA replication initiation in mammalian cells.
- Their specific role in early vertebrate development remained largely unknown.
Purpose of the Study:
- To investigate the function of Y RNAs in DNA replication during early development of Xenopus laevis and zebrafish.
- To determine the developmental timing and molecular mechanisms of Y RNA involvement in vertebrate DNA replication.
Main Methods:
- Utilized antisense morpholino nucleotides (MOs) to inhibit Y RNA function in developing embryos.
- Examined DNA replication, protein-binding interactions (ORC, Cdt1, HMGA1a), and chromatin association before and after the midblastula transition (MBT).
Main Results:
- Y RNA inhibition caused developmental arrest at the MBT due to DNA replication failure.
- Y RNAs are not required in early extracts but become essential post-MBT.
- Y RNAs associate with interphase nuclei post-MBT in an ORC-dependent manner and their MOs disrupt interactions with ORC, Cdt1, and HMGA1a.
Conclusions:
- The midblastula transition (MBT) marks a switch from Y RNA-independent to Y RNA-dependent DNA replication control in vertebrates.
- Y RNAs act as a developmentally regulated mechanism controlling the conserved eukaryotic DNA replication machinery.
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