Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Corrensstr. 3, 06466 Seeland, Germany.
Nordic Genetic Resource Center, SE-23053 Alnarp, Sweden.
Curr Biol. 2024 Jun 3;34(11):2344-2358.e5. doi: 10.1016/j.cub.2024.04.083. Epub 2024 May 22.
Inflorescence architecture and crop productivity are often tightly coupled in our major cereal crops. However, the underlying genetic mechanisms controlling cereal inflorescence development remain poorly understood. Here, we identified recessive alleles of barley (Hordeum vulgare L.) HvALOG1 (Arabidopsis thaliana LSH1 and Oryza G1) that produce non-canonical extra spikelets and fused glumes abaxially to the central spikelet from the upper-mid portion until the tip of the inflorescence. Notably, we found that HvALOG1 exhibits a boundary-specific expression pattern that specifically excludes reproductive meristems, implying the involvement of previously proposed localized signaling centers for branch regulation. Importantly, during early spikelet formation, non-cell-autonomous signals associated with HvALOG1 expression may specify spikelet meristem determinacy, while boundary formation of floret organs appears to be coordinated in a cell-autonomous manner. Moreover, barley ALOG family members synergistically modulate inflorescence morphology, with HvALOG1 predominantly governing meristem maintenance and floral organ development. We further propose that spatiotemporal redundancies of expressed HvALOG members specifically in the basal inflorescence may be accountable for proper patterning of spikelet formation in mutant plants. Our research offers new perspectives on regulatory signaling roles of ALOG transcription factors during the development of reproductive meristems in cereal inflorescences.
花序结构和作物产量在我们的主要粮食作物中通常紧密相关。然而,控制谷类花序发育的潜在遗传机制仍知之甚少。在这里,我们鉴定了大麦(Hordeum vulgare L.)HvALOG1(拟南芥 LSH1 和 Oryza G1)的隐性等位基因,该基因产生非典型的额外小穗,并将腹面的融合颖壳从花序的中上部分一直延伸到顶端小穗。值得注意的是,我们发现 HvALOG1 表现出特异的边界表达模式,专门排除生殖分生组织,暗示了以前提出的用于分枝调节的局部信号中心的参与。重要的是,在早期小穗形成过程中,与 HvALOG1 表达相关的非细胞自主信号可能特异地指定小穗分生组织的确定性,而小花器官的边界形成似乎以细胞自主的方式协调。此外,大麦ALOG 家族成员协同调节花序形态,HvALOG1 主要控制分生组织维持和花器官发育。我们进一步提出,在突变体植物中,表达的 HvALOG 成员在基部花序中的时空冗余可能是小穗形成正确模式化的原因。我们的研究为 ALOG 转录因子在谷类花序生殖分生组织发育过程中的调控信号作用提供了新的视角。