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Series GSE135962 Query DataSets for GSE135962
Status Public on Feb 14, 2020
Title Plant 22-nt siRNAs mediate translational repression and stress adaptation
Organism Arabidopsis thaliana
Experiment type Expression profiling by high throughput sequencing
Other
Summary Small interfering RNAs (siRNAs) are critical for proper development and immunity in eukaryotes1. Plants produce siRNAs with lengths of 21-, 22-, or 24- nucleotides (nt), wherein the 21- and 24-nt siRNAs mediate mRNA cleavage and DNA methylation2,3, respectively. However, the biological functions of 22-nt siRNAs remain elusive. Here we report the identification and characterization of a group of endogenous 22-nt siRNAs generated from the action of DICER-LIKE 2 (DCL2). When cytoplasmic RNA decay and DCL4 are deficient, the massive accumulation of 22-nt siRNAs causes pleiotropic growth disorders, including severe dwarfism, meristem defect, and pigmentation. Notably, two genes that encode nitrate reductases, NIA1 and NIA2, produce nearly half of the total of 22-nt siRNAs. Production of 22-nt siRNA triggers explosive self-amplification that leads to a small RNA storm, and induces dramatic translational repression both gene-specifically and globally. 22-nt siRNAs are also found to preferentially accumulate upon nitrogen deficiency, which acts to restrain plant growth and promote stress responses. Thus, our research uncovers the unique properties of 22-nt siRNAs, a previously unexplored class of plant siRNAs, and highlights the length of small RNA as a major functional determinant.
 
Overall design Col-0, ein5-1 dcl4-2 and ein5-1 dcl4-2 dcl2-1were grown on the MS medium for 6 days and then were transferred to the soil for another 14 days. Aerial parts of 20-day-old plant were collected at 15:00 for AGO1-associated small RNA isolation. Two biological replicates were prepared for each genotype. Library preparation and high-throughput sequencing were conducted in accordance with the manufacturers’ instructions. Total RNA was extracted using the Trizol and precipitated by ethonal. Sequencing libraries were prepared using the NEBNext® Small RNA Library Prep Set for Illumina. RNA quality and library quality were examined by a Bioanalyzer 2100 instrument (Agilent), and paired-end, 150-bp deep sequencing was performed on an Illumina Nova6000 platform.
 
Contributor(s) Wu H, Li B, Guo H
Citation(s) 32376953, 38637717
Submission date Aug 19, 2019
Last update date May 01, 2024
Contact name Bosheng Li
E-mail(s) libs@sustc.edu.cn
Organization name SUSTC (current, may different with previous institution )
Department MCDB
Street address SUStech Huiyuan #1 406
City Shenzhen
State/province Guangdong
ZIP/Postal code 581055
Country China
 
Platforms (1)
GPL26208 Illumina NovaSeq 6000 (Arabidopsis thaliana)
Samples (6)
GSM4038527 Col-0 AGO1 IP aerial part_rep1 (AGO1-associated small RNAs)
GSM4038528 Col-0 AGO1 IP aerial part_rep2 (AGO1-associated small RNAs)
GSM4038529 ein5 dcl4 AGO1 IP aerial part_rep1 (AGO1-associated small RNAs)
This SubSeries is part of SuperSeries:
GSE136164 Plant 22-nt siRNAs mediate translational repression and stress adaptation
Relations
BioProject PRJNA560787
SRA SRP218724

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Supplementary file Size Download File type/resource
GSE135962_AGO1_IP_processed_data.xlsx 2.8 Mb (ftp)(http) XLSX
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Raw data are available in SRA
Processed data are available on Series record

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