Bacteria-responsive microRNAs regulate plant innate immunity by modulating plant hormone networks

Weixiong Zhang(Washington University in St. Louis), Shang Gao(University of California, Riverside), Xiang Zhou(Washington University in St. Louis), Chellappan Padmanabhan(University of California, Riverside), Zheng Chen(Washington University in St. Louis), Xuefeng Zhou(Washington University in St. Louis), Xiaoming Zhang(University of California, Riverside), Nyssa Fromuth(University of California, Riverside), Gabriela Coutino(University of California, Riverside), Michael D. Coffey(University of California, Riverside), Hailing Jin(University of California, Riverside)
Plant Molecular Biology
December 10, 2010
Cited by 255Open Access
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Abstract

MicroRNAs (miRNAs) are key regulators of gene expression in development and stress responses in most eukaryotes. We globally profiled plant miRNAs in response to infection of bacterial pathogen Pseudomonas syringae pv. tomato (Pst). We sequenced 13 small-RNA libraries constructed from Arabidopsis at 6 and 14 h post infection of non-pathogenic, virulent and avirulent strains of Pst. We identified 15, 27 and 20 miRNA families being differentially expressed upon Pst DC3000 hrcC, Pst DC3000 EV and Pst DC3000 avrRpt2 infections, respectively. In particular, a group of bacteria-regulated miRNAs targets protein-coding genes that are involved in plant hormone biosynthesis and signaling pathways, including those in auxin, abscisic acid, and jasmonic acid pathways. Our results suggest important roles of miRNAs in plant defense signaling by regulating and fine-tuning multiple plant hormone pathways. In addition, we compared the results from sequencing-based profiling of a small set of miRNAs with the results from small RNA Northern blot and that from miRNA quantitative RT-PCR. Our results showed that although the deep-sequencing profiling results are highly reproducible across technical and biological replicates, the results from deep sequencing may not always be consistent with the results from Northern blot or miRNA quantitative RT-PCR. We discussed the procedural differences between these techniques that may cause the inconsistency.


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