| Literature DB >> 28635129 |
Yuanhao Ding1, Yizan Ma1, Nian Liu1, Jiao Xu1, Qin Hu1, Yaoyao Li1, Yuanlong Wu1, Sai Xie1, Longfu Zhu1, Ling Min1, Xianlong Zhang1.
Abstract
Male sterility caused by long-term high-temperature (HT) stress occurs widely in crops. MicroRNAs (miRNAs), a class of endogenous non-coding small RNAs, play an important role in the plant response to various abiotic stresses. To dissect the working principle of miRNAs in male sterility under HT stress in cotton, a total of 112 known miRNAs, 270 novel miRNAs and 347 target genes were identified from anthers of HT-insensitive (84021) and HT-sensitive (H05) cotton cultivars under normal-temperature and HT conditions through small RNA and degradome sequencing. Quantitative reverse transcriptase-polymerase chain reaction and 5'-RNA ligase-mediated rapid amplification of cDNA ends experiments were used to validate the sequencing data. The results show that miR156 was suppressed by HT stress in both 84021 and H05; miR160 was suppressed in 84021 but induced in H05. Correspondingly, SPLs (target genes of miR156) were induced both in 84021 and H05; ARF10 and ARF17 (target genes of miR160) were induced in 84021 but suppressed in H05. Overexpressing miR160 increased cotton sensitivity to HT stress seen as anther indehiscence, associated with the suppression of ARF10 and ARF17 expression, thereby activating the auxin response that leads to anther indehiscence. Supporting this role for auxin, exogenous Indole-3-acetic acid (IAA) leads to a stronger male sterility phenotype both in 84021 and H05 under HT stress. Cotton plants overexpressing miR157 suppressed the auxin signal, and also showed enhanced sensitivity to HT stress, with microspore abortion and anther indehiscence. Thus, we propose that the auxin signal, mediated by miRNAs, is essential for cotton anther fertility under HT stress.Entities:
Keywords: zzm321990Gossypium hirsutumzzm321990; auxin signal; degradome sequencing; high-temperature stress; male sterility; miR156/157; miR160; miRNA sequencing; miRNAs
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Year: 2017 PMID: 28635129 DOI: 10.1111/tpj.13620
Source DB: PubMed Journal: Plant J ISSN: 0960-7412 Impact factor: 6.417