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

Author:

Hsieh Li-Ching1,Lin Shu-I.1,Shih Arthur Chun-Chieh1,Chen June-Wei1,Lin Wei-Yi1,Tseng Ching-Ying1,Li Wen-Hsiung1,Chiou Tzyy-Jen1

Affiliation:

1. Genomics Research Center, Academia Sinica, Taipei 115, Taiwan (L.-C.H., W.-H.L.); Agricultural Biotechnology Research Center, Academia Sinica, Taipei 115, Taiwan (S.-I.L., J.-W.C., W.-Y.L., C.-Y.T., T.-J.C.); Graduate Institute of Life Sciences, National Defense Medical Center, Taipei 114, Taiwan (S.-I.L., T.-J.C.); Institute of Information Science, Academia Sinica, Taipei 115, Taiwan (A.C.-C.S.)

Abstract

Abstract 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.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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