Novel phosphate deficiency-responsive long non-coding RNAs in the legume model plant Medicago truncatula

© The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology.

Bibliographische Detailangaben
Veröffentlicht in:Journal of experimental botany. - 1985. - 68(2017), 21-22 vom: 16. Dez., Seite 5937-5948
1. Verfasser: Wang, Tianzuo (VerfasserIn)
Weitere Verfasser: Zhao, Mingui, Zhang, Xiuxiu, Liu, Min, Yang, Chenge, Chen, Yuhui, Chen, Rujin, Wen, Jiangqi, Mysore, Kirankumar S, Zhang, Wen-Hao
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Journal of experimental botany
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. High-throughput sequencing Medicago truncatula legume plants long non-coding RNAs (lncRNAs) phosphate acquisition phosphate deficiency Phosphates mehr... RNA, Long Noncoding RNA, Plant
Beschreibung
Zusammenfassung:© The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology.
Emerging evidence indicates that long non-coding RNAs (lncRNAs) play important roles in the regulation of many biological processes. Inhibition of plant growth due to deficiency in soil inorganic phosphate (Pi) occurs widely across natural and agricultural ecosystems; however, we know little about the function of plant lncRNAs in response to Pi deficiency. To address this issue, we first identified 10 785 lncRNAs in the legume model species Medicago truncatula by sequencing eight strand-specific libraries. Out of these lncRNAs, 358 and 224 were responsive to Pi deficiency in the leaves and roots, respectively. We further predicted and classified the putative targets of those lncRNAs and the results revealed that they may be involved in the processes of signal transduction, energy synthesis, detoxification, and Pi transport. Finally, we functionally characterized three Phosphate Deficiency-Induced LncRNAs (PDILs) using their corresponding Tnt1 mutants. The results showed that PDIL1 suppressed degradation of MtPHO2, which encodes a ubiquitin-conjugating E2 enzyme regulated by miR399, while PDIL2 and PDIL3 directly regulated Pi transport at the transcriptional level. These findings demonstrate that PDILs can regulate Pi-deficiency signaling and Pi transport, highlighting the involvement of lncRNAs in the regulation of responses of plants to Pi deficiency
Beschreibung:Date Completed 07.01.2019
Date Revised 07.01.2019
published: Print
Citation Status MEDLINE
ISSN:1460-2431
DOI:10.1093/jxb/erx384