TY - JOUR
T1 - The RNA Polymerase II C-Terminal Domain Phosphatase-Like Protein FIERY2/CPL1 Interacts with eIF4AIII and Is Essential for Nonsense-Mediated mRNA Decay in Arabidopsis
AU - Cui, Peng
AU - Chen, Tao
AU - Qin, Tao
AU - Ding, Feng
AU - Wang, Zhenyu
AU - Chen, Hao
AU - Xiong, Liming
N1 - Funding information:
This work was supported by King Abdullah University of Science and Technology Office of Sponsored Research (OSR) under Award URF/1/2283-01-01 and Faculty Baseline Funds BAS/1/1007-1-1. We thank the Bioscience Core Lab of KAUST for providing genome sequencing and imaging services.
Publisher Copyright:
© 2016 American Society of Plant Biologists. All rights reserved.
© The Author(s) 2016.
PY - 2016/3
Y1 - 2016/3
N2 - Nonsense-mediated decay (NMD) is
a posttranscriptional surveillance mechanism in eukaryotes that recognizes and
degrades transcripts with premature translation-termination codons. The RNA
polymerase II C-terminal domain phosphatase-like protein FIERY2 (FRY2; also
known as C-TERMINAL DOMAIN PHOSPHATASE-LIKE1 [CPL1]) plays multiple roles in
RNA processing in Arabidopsis thaliana. Here, we found that
FRY2/CPL1 interacts with two NMD factors,
eIF4AIII and UPF3, and is involved in the dephosphorylation of eIF4AIII. This
dephosphorylation retains eIF4AIII in the nucleus and limits its accumulation
in the cytoplasm. By analyzing RNA-seq data combined with quantitative RT-PCR
validation, we found that a subset of alternatively spliced transcripts and
5′-extended mRNAs with NMD-eliciting features
accumulated in the fry2-1 mutant, cycloheximide-treated wild
type, and upf3 mutant plants, indicating that FRY2 is
essential for the degradation of these NMD transcripts.
AB - Nonsense-mediated decay (NMD) is
a posttranscriptional surveillance mechanism in eukaryotes that recognizes and
degrades transcripts with premature translation-termination codons. The RNA
polymerase II C-terminal domain phosphatase-like protein FIERY2 (FRY2; also
known as C-TERMINAL DOMAIN PHOSPHATASE-LIKE1 [CPL1]) plays multiple roles in
RNA processing in Arabidopsis thaliana. Here, we found that
FRY2/CPL1 interacts with two NMD factors,
eIF4AIII and UPF3, and is involved in the dephosphorylation of eIF4AIII. This
dephosphorylation retains eIF4AIII in the nucleus and limits its accumulation
in the cytoplasm. By analyzing RNA-seq data combined with quantitative RT-PCR
validation, we found that a subset of alternatively spliced transcripts and
5′-extended mRNAs with NMD-eliciting features
accumulated in the fry2-1 mutant, cycloheximide-treated wild
type, and upf3 mutant plants, indicating that FRY2 is
essential for the degradation of these NMD transcripts.
UR - http://www.scopus.com/inward/record.url?scp=84962850768&partnerID=8YFLogxK
U2 - 10.1105/tpc.15.00771
DO - 10.1105/tpc.15.00771
M3 - Journal article
C2 - 26887918
AN - SCOPUS:84962850768
SN - 1040-4651
VL - 28
SP - 770
EP - 785
JO - Plant Cell
JF - Plant Cell
IS - 3
ER -