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Distinct replication-independent and -dependent phases of histone gene expression during the Physarum cell cycle
Abstract:
During the S phase of the cell cycle, histone gene expression and DNA replication are tightly coupled. In mitotically synchronous plasmodia of the myxomycete Physarum polycephalum, which has no G1 phase, histone mRNA synthesis begins in mid-G2 phase. Although histone gene transcription is activated in the absence of significant DNA synthesis, our data demonstrate that histone gene expression became tightly coupled to DNA replication once the S phase began. There was a transition from the replication-independent phase to the replication-dependent phase of histone gene expression. During the first phase, histone mRNA synthesis appears to be under direct cell cycle control; it was not coupled to DNA replication. This allowed a pool of histone mRNA to accumulate in late G2 phase, in anticipation of future demand. The second phase began at the end of mitosis, when the S phase began, and expression became homeostatically coupled to DNA replication. This homeostatic control required continuing protein synthesis, since cycloheximide uncoupled transcription from DNA synthesis. Nuclear run-on assays suggest that in P. polycephalum this coupling occurs at the level of transcription. While histone gene transcription appears to be directly switched on in mid-G2 phase and off at the end of the S phase by cell cycle regulators, only during the S phase was the level of transcription balanced with the rate of DNA synthesis.
Insights
Histone gene expression in Physarum polycephalum transitions from cell cycle control to DNA replication coupling during the S phase. This ensures sufficient histone mRNA is available for DNA synthesis.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Histone gene expression is crucial for DNA replication during the S phase of the cell cycle.
- The myxomycete Physarum polycephalum lacks a G1 phase, offering a unique model for studying cell cycle regulation.
Purpose of the Study:
- To investigate the coupling between histone gene expression and DNA replication in Physarum polycephalum.
- To determine the regulatory mechanisms controlling histone mRNA synthesis throughout the cell cycle.
Main Methods:
- Utilizing mitotically synchronous plasmodia of Physarum polycephalum.
- Employing cycloheximide treatment to assess the role of protein synthesis.
- Performing nuclear run-on assays to analyze transcriptional regulation.
Main Results:
- Histone mRNA synthesis begins in mid-G2 phase, independent of DNA replication.
- Expression becomes tightly coupled to DNA replication once the S phase commences.
- This coupling requires ongoing protein synthesis and occurs at the transcriptional level.
Conclusions:
- Physarum polycephalum exhibits a two-phase regulation of histone gene expression: replication-independent in G2 and replication-dependent during S phase.
- Cell cycle regulators control the precise timing of histone gene transcription.
- Homeostatic control ensures transcription matches DNA synthesis rates during S phase.