A pathway for the biogenesis of trans-acting siRNAs in Arabidopsis.
By M. Yoshikawa, A. Peragine, M. Park, R. Poethig. Genes & Development, 2005
758 citations recorded by the source corpus.
The Arabidopsis genes, TAS2 and TAS1a, produce structurally similar noncoding transcripts that are transformed into short (21-nucleotide [nt]) and long (24-nt) siRNAs by RNA silencing pathways. Some of these short siRNAs direct the cleavage of protein-coding transcripts, and thus function as trans-acting siRNAs (ta-siRNAs). Using genetic analysis, we defined the pathway by which ta-siRNAs and other short siRNAs are generated from these loci. This process is initiated by the miR173-directed cleavage of a primary poly(A) transcript. The 3' fragment is then transformed into short siRNAs by the sequential activity of SGS3, RDR6, and DCL4: SGS3 stabilizes the fragment, RDR6 produces a complementary strand, and DCL4 cleaves the resulting double-stranded molecule into short siRNAs, starting at the end with the miR173 cleavage site and proceeding in 21-nt increments from this point. The 5' cleavage fragment is also processed by this pathway, but less efficiently. The DCL3-dependent pathway that generates long siRNAs does not require miRNA-directed cleavage and plays a minor role in the silencing of these loci. Our results define the core components of a post-transcriptional gene silencing pathway in Arabidopsis and reveal some of the features that direct transcripts to this pathway.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/73490c362ac9d422aebea68c4788a324a1e6bc93
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In Molecular Biology
- Jian‐Kang Zhu
- Xuemei Chen
- David P. Bartel
- Ramanjulu Sunkar
- H. Vaucheret
- Olivier Voinnet
- James C. Carrington
- R. Poethig
In Plant Science
- Jian‐Kang Zhu
- Olivier Voinnet
- Xuemei Chen
- Ramanjulu Sunkar
- David P. Bartel
- H. Vaucheret
- Michael J. Axtell
- James C. Carrington
Citations in the corpus
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