Publications by authors named "Dai Tsukioka"

Phosphorylated H2AX, known as γH2AX, forms in response to genotoxic insults in somatic cells. Despite the high abundance of H2AX in zygotes, the level of irradiation-induced γH2AX is low at this stage. Another H2A variant, TH2A, is present at a high level in zygotes and can also be phosphorylated at its carboxyl end.

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Article Synopsis
  • In somatic cells, DNA repair is reduced during mitosis to avoid issues like anaphase bridges, which can disrupt the separation of chromosomes.
  • Research shows that while γH2AX signals (markers of DNA damage) linger in somatic cells, they peak and diminish quickly in mouse zygotes, suggesting their DNA repair process is effective even during mitosis.
  • The lack of H2AX was found to improve the separation of sister chromatids and embryo development, indicating that the DNA repair system in zygotes is uniquely regulated to eliminate damaged cells and prevent mutation transmission to future generations.
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In mice, transcription initiates at the mid-one-cell stage and transcriptional activity dramatically increases during the two-cell stage, a process called zygotic gene activation (ZGA). Associated with ZGA is a marked change in the pattern of gene expression that occurs after the second round of DNA replication. To distinguish ZGA before and after the second-round DNA replication, the former and latter are called minor and major ZGA, respectively.

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Dopa decarboxylase (DDC) protein is involved in the synthesis of dopamine and serotonin. Here, we show that in the silkworm Bombyx mori, a novel DDC splicing variant is selectively expressed in the brain and subesophageal ganglia. In Drosophila melanogaster, a neuron-specific isoform of DDC is known to be alternatively spliced in a similar manner.

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