Ta-siRNAs are generated from non-coding transcripts through
Argonaute-mediated
miRNA-guided cleavage followed by conversion to double stranded RNA by RDR6. The resulting dsRNA is further processed by the
Dicer-like 4 (DCL4) enzyme to produce a phased array of 21-nt
siRNAs from positions adjoining the miRNA cleavage site. There are four families of ta-siRNA-generating loci (
TAS genes) in
A. thaliana. TAS1, TAS2, and TAS4 families require one miRNA binding site for cleavage to occur while TAS3 requires two binding sites. TAS gene family numbers do not generally indicate
orthology, e.g. the moss
TAS1 gene family does not share an ancestor gene with the
Arabidopsis thaliana TAS1 gene family.
TAS1 and TAS2 TAS1/2 transcripts undergo an initial AGO1 mediated cleavage at the 5' end that is guided by miR173. RDR6 then converts the transcript into a double strand RNA fragment which then gets processed by DCL4 to generate the 21-nt siRNA with 2 nucleotide 3' overhangs that target complementary mRNAs in trans.
TAS4 The initial steps for the TAS4 family of ta-siRNA is similar to that of TAS1 and TAS2. The TAS4 family of transcripts first undergo miR828 guided, AGO1 mediated cleavage, followed by dsRNA synthesis and processing by DCL4.
TAS3 In contrast to the single mRNA binding family, TAS3 requires the guide mRNA miR390 bind the transcript at two sites. The transcript is then cleaved at the 3' binding site only, by AGO7. As is the case for the TAS1, TAS2, and TAS3 families, RDR6 then synthesizes the dsRNA fragment which is further processed by DCL4. == Mechanism ==