4.7 Article

Systematic characterization of novel lncRNAs responding to phosphate starvation in Arabidopsis thaliana

Journal

BMC GENOMICS
Volume 17, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12864-016-2929-2

Keywords

Long ncRNAs; RNA-Seq; Phosphate starvation; Arabidopsis thaliana; Poly(A); Poly(A)-

Funding

  1. National Key Basic Research Program of China [2012CB316503]
  2. National High-Tech Research and Development Program of China [2014AA021103]
  3. National Natural Science Foundation of China [31271402, 31522030]
  4. Tsinghua University Initiative Scientific Research Program [2014z21045]
  5. Computing Platform of National Protein Facilities (Tsinghua University)

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Background: Previously, several long non-coding RNAs (lncRNAs) were characterized as regulators in phosphate (Pi) starvation responses. However, systematic studies of novel lncRNAs involved in the Pi starvation signaling pathways have not been reported. Results: Here, we used a genome-wide sequencing and bioinformatics approach to identify both poly(A) + and poly(A)- lncRNAs that responded to Pi starvation in Arabidopsis thaliana. We sequenced shoot and root transcriptomes of the Arabidopsis seedlings grown under Pi-sufficient and Pi-deficient conditions, and predicted 1212 novel lncRNAs, of which 78 were poly(A)- lncRNAs. By employing strand-specific RNA libraries, we discovered many novel antisense lncRNAs for the first time. We further defined 309 lncRNAs that were differentially expressed between P+ and P- conditions in either shoots or roots. Through Gene Ontology enrichment of the associated protein-coding genes (co-expressed or close on the genome), we found that many lncRNAs were adjacent or co-expressed with the genes involved in several Pi starvation related processes, including cell wall organization and photosynthesis. In total, we identified 104 potential lncRNA targets of PHR1, a key regulator for transcriptional response to Pi starvation. Moreover, we identified 16 candidate lncRNAs as potential targets of miR399, another key regulator of plant Pi homeostasis. Conclusions: Altogether, our data provide a rich resource of candidate lncRNAs involved in the Pi starvation regulatory network.

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