TY - JOUR
T1 - ARGONAUTE PIWI domain and microRNA duplex structure regulate small RNA sorting in Arabidopsis
AU - Zhang, Xiaoming
AU - Niu, Dong Dong
AU - Carbonell, Alberto
AU - Wang, Airong
AU - Lee, Angel
AU - Tun, Vinnary
AU - Wang, Zonghua
AU - Carrington, James C.
AU - Chang, Chia En A.
AU - Jin, Hailing
N1 - Publisher Copyright:
© 2014 Macmillan Publishers Limited. All rights reserved.
PY - 2014/11/19
Y1 - 2014/11/19
N2 - Small RNAs (sRNAs) are loaded into ARGONAUTE (AGO) proteins to induce gene silencing. In plants, the 50-terminal nucleotide is important for sRNA sorting into different AGOs. Here we show that microRNA (miRNA) duplex structure also contributes to miRNA sorting. Base pairing at the 15th nucleotide of a miRNA duplex is important for miRNA sorting in both Arabidopsis AGO1 and AGO2. AGO2 favours miRNA duplexes with no middle mismatches, whereas AGO1 tolerates, or prefers, duplexes with central mismatches. AGO structure modelling and mutational analyses reveal that the QF-V motif within the conserved PIWI domain contributes to recognition of base pairing at the 15th nucleotide of a duplex, while the DDDE catalytic core of AtAGO2 is important for recognition of the central nucleotides. Finally, we rescued the adaxialized phenotype of ago1-12, which is largely due to miR165 loss-of-function, by changing miR165 duplex structure which we predict redirects it to AGO2.
AB - Small RNAs (sRNAs) are loaded into ARGONAUTE (AGO) proteins to induce gene silencing. In plants, the 50-terminal nucleotide is important for sRNA sorting into different AGOs. Here we show that microRNA (miRNA) duplex structure also contributes to miRNA sorting. Base pairing at the 15th nucleotide of a miRNA duplex is important for miRNA sorting in both Arabidopsis AGO1 and AGO2. AGO2 favours miRNA duplexes with no middle mismatches, whereas AGO1 tolerates, or prefers, duplexes with central mismatches. AGO structure modelling and mutational analyses reveal that the QF-V motif within the conserved PIWI domain contributes to recognition of base pairing at the 15th nucleotide of a duplex, while the DDDE catalytic core of AtAGO2 is important for recognition of the central nucleotides. Finally, we rescued the adaxialized phenotype of ago1-12, which is largely due to miR165 loss-of-function, by changing miR165 duplex structure which we predict redirects it to AGO2.
UR - http://www.scopus.com/inward/record.url?scp=84922319019&partnerID=8YFLogxK
U2 - 10.1038/ncomms6468
DO - 10.1038/ncomms6468
M3 - Article
C2 - 25406978
AN - SCOPUS:84922319019
SN - 2041-1723
VL - 5
JO - Nature communications
JF - Nature communications
M1 - 5468
ER -