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Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
Published on: April 29, 2010
The poly(A) polymerase PAPS1 interacts with the RNA-directed DNA-methylation pathway in sporophyte and pollen
Yunming Zhang1, Anna Ramming1, Lisa Heinke1
1Institute for Biochemistry and Biology, University of Potsdam, Karl-Liebknecht-Str. 24-25, D-14476, Potsdam-Golm, Germany.
Abstract:
RNA-based processes play key roles in the regulation of eukaryotic gene expression. This includes both the processing of pre-mRNAs into mature mRNAs ready for translation and RNA-based silencing processes, such as RNA-directed DNA methylation (RdDM). Polyadenylation of pre-mRNAs is one important step in their processing and is carried out by three functionally specialized canonical nuclear poly(A) polymerases in Arabidopsis thaliana. Null mutations in one of these, termed PAPS1, result in a male gametophytic defect. Using a fluorescence-labelling strategy, we have characterized this defect in more detail using RNA and small-RNA sequencing. In addition to global defects in the expression of pollen-differentiation genes, paps1 null-mutant pollen shows a strong overaccumulation of transposable element (TE) transcripts, yet a depletion of 21- and particularly 24-nucleotide-long short interfering RNAs (siRNAs) and microRNAs (miRNAs) targeting the corresponding TEs. Double-mutant analyses support a specific functional interaction between PAPS1 and components of the RdDM pathway, as evident from strong synergistic phenotypes in mutant combinations involving paps1, but not paps2 paps4, mutations. In particular, the double-mutant of paps1 and rna-dependent rna polymerase 6 (rdr6) shows a synergistic developmental phenotype disrupting the formation of the transmitting tract in the female gynoecium. Thus, our findings in A. thaliana uncover a potentially general link between canonical poly(A) polymerases as components of mRNA processing and RdDM, reflecting an analogous interaction in fission yeast.
Insights
Polyadenylation factor PAPS1 is crucial for male fertility in Arabidopsis. Its mutation disrupts gene expression and RNA silencing, revealing a link between mRNA processing and DNA methylation pathways.
Area of Science:
- Plant molecular biology
- Epigenetics
- Gene expression regulation
Background:
- RNA-based processes, including mRNA processing and RNA-directed DNA methylation (RdDM), are vital for eukaryotic gene expression.
- Canonical nuclear poly(A) polymerases (PAPs) in Arabidopsis thaliana are essential for pre-mRNA polyadenylation, a key processing step.
- Null mutations in PAPS1, one of these PAPs, lead to male gametophytic defects.
Purpose of the Study:
- To investigate the molecular mechanisms underlying the male gametophytic defect caused by PAPS1 mutations.
- To explore the relationship between polyadenylation and RNA-directed DNA methylation (RdDM) pathways.
Main Methods:
- Fluorescence-labeling strategy
- RNA sequencing
- Small-RNA sequencing
- Double-mutant analyses
Main Results:
- paps1 null mutants exhibit global defects in pollen-differentiation gene expression.
- paps1 mutants show increased transposable element (TE) transcripts but decreased TE-targeting small interfering RNAs (siRNAs) and microRNAs (miRNAs).
- Synergistic phenotypes in paps1 double mutants with RdDM pathway components (e.g., rdr6) highlight functional interactions.
Conclusions:
- Canonical poly(A) polymerases like PAPS1 are linked to mRNA processing and the RdDM pathway in Arabidopsis.
- This interaction between mRNA processing and epigenetic regulation is conserved, as suggested by analogous findings in fission yeast.
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