Novel Stress-Inducible Antisense RNAs of Protein-Coding Loci Are Synthesized by RNA-Dependent RNA Polymerase1[OPEN]
Novel Stress-Inducible Antisense RNAs of Protein-Coding Loci Are Synthesized by RNA-Dependent RNA Polymerase1[OPEN]
复制标题
RNA 依赖性 RNA 聚合酶合成蛋白质编码位点的新型应激诱导反义 RNA1[打开]
作者:
A. Matsui;K. Iida;Maho Tanaka;K. Yamaguchi;Kayoko Mizuhashi;Jong;S. Takahashi;Norio Kobayashi;S. Shigenobu;K. Shinozaki;M. Seki
Stress-inducible non-coding antisense RNAs generated by RNA-dependent RNA polymerases function in a novel abiotic stress response mechanism different from the known endogenous small RNA pathways. Our previous study identified approximately 6,000 abiotic stress-responsive noncoding transcripts existing on the antisense strand of protein-coding genes and implied that a type of antisense RNA was synthesized from a sense RNA template by RNA-dependent RNA polymerase (RDR). Expression analyses revealed that the expression of novel abiotic stress-induced antisense RNA on 1,136 gene loci was reduced in the rdr1/2/6 mutants. RNase protection indicated that the RD29A antisense RNA and other RDR1/2/6-dependent antisense RNAs are involved in the formation of dsRNA. The accumulation of stress-inducible antisense RNA was decreased and increased in dcp5 and xrn4, respectively, but not changed in dcl2/3/4, nrpd1a and nrpd1b. RNA-seq analyses revealed that the majority of the RDR1/2/6-dependent antisense RNA loci did not overlap with RDR1/2/6-dependent 20–30 nt RNA loci. Additionally, rdr1/2/6 mutants decreased the degradation rate of the sense RNA and exhibited arrested root growth during the recovery stage following a drought stress, whereas dcl2/3/4 mutants did not. Collectively, these results indicate that RDRs have stress-inducible antisense RNA synthesis activity and a novel biological function that is different from the known endogenous small RNA pathways from protein-coding genes. These data reveal a novel mechanism of RNA regulation during abiotic stress response that involves complex RNA degradation pathways.
影响因子:
10.5
作者:
Yoshikawa, M;Peragine, A;Poethig, RS
通讯作者:
Poethig, RS
影响因子:
64.5
作者:
Autran, Daphne;Baroux, Celia;Grossniklaus, Ueli
通讯作者:
Grossniklaus, Ueli
影响因子:
4.5
作者:
Gu, Rui;Zhang, Zuo;Carmichael, Gordon G.
通讯作者:
Carmichael, Gordon G.