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Phased small RNA-mediated systemic signaling in plants.


ABSTRACT: Systemic acquired resistance (SAR) involves the generation of systemically transported signal that arms distal plant parts against secondary infections. We show that two phased 21-nucleotide (nt) trans-acting small interfering RNA3a RNAs (tasi-RNA) derived from TAS3a and synthesized within 3 hours of pathogen infection are the early mobile signal in SAR. TAS3a undergoes alternate polyadenylation, resulting in the generation of 555- and 367-nt transcripts. The 555-nt transcripts likely serves as the sole precursor for tasi-RNAs D7 and D8, which cleave Auxin response factors (ARF) 2, 3, and 4 to induce SAR. Conversely, increased expression of ARF3 represses SAR. Knockout mutations in TAS3a or RNA silencing components required for tasi-RNA biogenesis compromise SAR without altering levels of known SAR-inducing chemicals. Both tasi-ARFs and the 367-nt transcripts are mobile and transported via plasmodesmata. Together, we show that tasi-ARFs are the early mobile signal in SAR.

SUBMITTER: Shine MB 

PROVIDER: S-EPMC9232115 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Phased small RNA-mediated systemic signaling in plants.

Shine M B MB   Zhang Kai K   Liu Huazhen H   Lim Gah-Hyun GH   Xia Fan F   Yu Keshun K   Hunt Arthur G AG   Kachroo Aardra A   Kachroo Pradeep P  

Science advances 20220624 25


Systemic acquired resistance (SAR) involves the generation of systemically transported signal that arms distal plant parts against secondary infections. We show that two phased 21-nucleotide (nt) <i>trans-acting small interfering RNA3a</i> RNAs (tasi-RNA) derived from <i>TAS3a</i> and synthesized within 3 hours of pathogen infection are the early mobile signal in SAR. <i>TAS3a</i> undergoes alternate polyadenylation, resulting in the generation of 555- and 367-nt transcripts. The 555-nt transcri  ...[more]

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