Han Yingjia, Jiang Siqi, Dong Xiaomei, Dai Xing, Wang Shunxi, Zheng Ying, Yan Ge, Li Shengben, Wu Liuji, Walbot Virginia, Meyers Blake C, Zhang Mei
Key Laboratory of Plant Molecular Physiology, Institute of Botany, The Chinese Academy of Sciences, Beijing 100093, China.
China National Botanical Garden, Beijing 100093, China.
Plant Cell. 2024 Dec 23;37(1). doi: 10.1093/plcell/koae289.
Reproductive phasiRNAs (phased, secondary, small interfering RNAs), produced from numerous PHAS loci, are essential for plant anther development. PHAS transcripts are enriched on endoplasmic reticulum-bound ribosomes in maize (Zea mays), but the impact of ribosome binding on phasiRNA biogenesis remains elusive. Through ribosome profiling of maize anthers at 10 developmental stages, we demonstrated that 24-PHAS transcripts are bound by ribosomes, with patterns corresponding to the timing and abundance of 24-PHAS transcripts. Ribosome binding to 24-PHAS transcripts is conserved among different maize inbred lines, with ribosomes enriched upstream of the miR2275 target sites. We detected short open reading frames (sORFs) in the ribosome-binding regions of some 24-PHAS transcripts and observed a 3-nt periodicity in most sORFs, but mass spectrometry failed to detect peptides corresponding to the sORFs. Deletion of the entire ribosome-binding region of 24PHAS_NO296 locus eliminated ribosome binding and decreased 24-nt phasiRNA production, without affecting 24PHAS_NO296 transcript levels. In contrast, disrupting only the sORFs in 24PHAS_NO296 did not substantially affect the generation of 24-nt phasiRNAs. A newly formed sORF in these mutants may have re-directed ribosome binding to its transcripts. Overall, these findings demonstrate that sORFs facilitate ribosome binding to 24-PHAS transcripts, thereby promoting phasiRNA biogenesis in meiotic anthers.
从众多PHAS位点产生的生殖阶段小干扰RNA(phased, secondary, small interfering RNAs,phasiRNAs)对植物花药发育至关重要。在玉米(Zea mays)中,PHAS转录本在内质网结合核糖体上富集,但核糖体结合对phasiRNA生物合成的影响仍不清楚。通过对玉米花药10个发育阶段的核糖体图谱分析,我们证明24-PHAS转录本与核糖体结合,其模式与24-PHAS转录本的时间和丰度相对应。核糖体与24-PHAS转录本的结合在不同玉米自交系中是保守的,核糖体在miR2275靶位点上游富集。我们在一些24-PHAS转录本的核糖体结合区域检测到短开放阅读框(sORFs),并在大多数sORFs中观察到3个核苷酸的周期性,但质谱未能检测到与这些sORFs对应的肽段。删除24PHAS_NO296位点的整个核糖体结合区域消除了核糖体结合并降低了24核苷酸phasiRNA的产生,而不影响24PHAS_NO296转录本水平。相反,仅破坏24PHAS_NO296中的sORFs对24核苷酸phasiRNAs的产生没有实质性影响。这些突变体中新形成的sORF可能将核糖体结合重新导向其转录本。总体而言,这些发现表明sORFs促进核糖体与24-PHAS转录本的结合,从而促进减数分裂期花药中的phasiRNA生物合成。