Uncovering Small RNA-Mediated Responses to Phosphate Deficiency in Arabidopsis by Deep Sequencing

被引:571
作者
Hsieh, Li-Ching [2 ]
Lin, Shu-I [1 ,3 ]
Shih, Arthur Chun-Chieh [4 ]
Chen, June-Wei [1 ]
Lin, Wei-Yi [1 ,5 ,6 ]
Tseng, Ching-Ying [1 ]
Li, Wen-Hsiung [2 ,7 ,8 ]
Chiou, Tzyy-Jen [1 ,3 ,5 ,9 ]
机构
[1] Acad Sinica, Agr Biotechnol Res Ctr, Taipei 115, Taiwan
[2] Acad Sinica, Genom Res Ctr, Taipei 115, Taiwan
[3] Natl Def Med Ctr, Grad Inst Life Sci, Taipei 114, Taiwan
[4] Acad Sinica, Inst Informat Sci, Taipei 115, Taiwan
[5] Acad Sinica, Taiwan Int Grad Program, Mol & Biol Agr Sci Program, Taipei 115, Taiwan
[6] Natl Chung Hsing Univ, Grad Inst Biotechnol, Taichung 402, Taiwan
[7] Acad Sinica, Biodivers Res Ctr, Taipei 115, Taiwan
[8] Univ Chicago, Dept Ecol & Evolut, Chicago, IL 60637 USA
[9] Natl Chung Hsing Univ, Dept Life Sci, Taichung 402, Taiwan
关键词
TRANS-ACTING SIRNAS; TRANSLATIONAL INHIBITION; TRANSCRIPTION FACTOR; OXIDATIVE STRESS; MICRORNAS; IDENTIFICATION; CLEAVAGE; GENES; HOMEOSTASIS; MIRNA;
D O I
10.1104/pp.109.147280
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Recent studies have demonstrated the important role of plant microRNAs (miRNAs) under nutrient deficiencies. In this study, deep sequencing of Arabidopsis (Arabidopsis thaliana) small RNAs was conducted to reveal miRNAs and other small RNAs that were differentially expressed in response to phosphate (Pi) deficiency. About 3.5 million sequence reads corresponding to 0.6 to 1.2 million unique sequence tags from each Pi-sufficient or Pi-deficient root or shoot sample were mapped to the Arabidopsis genome. We showed that upon Pi deprivation, the expression of miR156, miR399, miR778, miR827, and miR2111 was induced, whereas the expression of miR169, miR395, and miR398 was repressed. We found cross talk coordinated by these miRNAs under different nutrient deficiencies. In addition to miRNAs, we identified one Pi starvation-induced DICER-LIKE1-dependent small RNA derived from the long terminal repeat of a retrotransposon and a group of 19-nucleotide small RNAs corresponding to the 5' end of tRNA and expressed at a high level in Pi-starved roots. Importantly, we observed an increased abundance of TAS4-derived trans-acting small interfering RNAs (ta-siRNAs) in Pi-deficient shoots and uncovered an autoregulatory mechanism of PAP1/MYB75 via miR828 and TAS4-siR81(-) that regulates the biosynthesis of anthocyanin. This finding sheds light on the regulatory network between miRNA/ta-siRNA and its target gene. Of note, a substantial amount of miR399* accumulated under Pi deficiency. Like miR399, miR399* can move across the graft junction, implying a potential biological role for miR399*. This study represents a comprehensive expression profiling of Pi-responsive small RNAs and advances our understanding of the regulation of Pi homeostasis mediated by small RNAs.
引用
收藏
页码:2120 / 2132
页数:13
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