State Key Laboratory for Agrobiotechnology and Key Laboratory of Crop Heterosis and Utilization (MOE) and Beijing Key Laboratory of Crop Genetic Improvement, China Agricultural University, Beijing, 100193, People's Republic of China.
Planta. 2021 Jan 22;253(2):44. doi: 10.1007/s00425-020-03531-x.
The function of SQUAMOSA PROMOTER-BINDING PROTEIN-BOX gene TaSPL14 in wheat is similar to that of OsSPL14 in rice in regulating plant height, panicle length, spikelet number, and thousand-grain weight of wheat, but differs during tiller development. TaSPL14 may regulate spike development via ethylene-response gene EIN3-LIKE 1 (TaEIL1), ETHYLENE-RESPONSIVE TRANSCRIPTION FACTOR 2.11 (TaRAP2.11), and ETHYLENE-RESPONSIVE TRANSCRIPTION FACTOR 1 (TaERF1), but not DENSE AND ERECT PANICLE 1 (TaDEP1) in wheat. The SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE gene OsSPL14 from rice is considered to be a major determinant of ideal plant architecture consisting of few unproductive tillers, more grains per spike, and high resistance of stems to lodging. However, the function of its orthologous gene, TaSPL14, in wheat is unknown. Here, we reported the functional similarities and differences between TaSPL14 and OsSPL14. Similar to OsSPL14 knock-outs in rice, wheat TaSPL14 knock-out plants exhibited decreased plant height, panicle length, spikelet number, and thousand-grain weight. In contrast to OsSPL14, however, TaSPL14 did not affect tiller number. Transcriptome analysis revealed that the expression of genes related to ethylene response was significantly decreased in young spikes of TaSPL14 knock-out lines as compared with wild type. TaSPL14 directly binds to the promoters of the ethylene-response genes TaEIL1, TaRAP2.11, and TaERF1, and promotes their expression, suggesting that TaSPL14 might regulate wheat spike development via the ethylene-response pathway. The elucidation of TaSPL14 will contribute to understanding of the molecular mechanisms that underlie wheat plant architecture.
小麦 SQUAMOSA PROMOTER-BINDING PROTEIN-BOX 基因 TaSPL14 的功能与水稻 OsSPL14 相似,可调节小麦株高、穗长、小穗数和千粒重,但在分蘖发育过程中存在差异。TaSPL14 可能通过乙烯应答基因 EIN3-LIKE 1(TaEIL1)、ETHYLENE-RESPONSIVE TRANSCRIPTION FACTOR 2.11(TaRAP2.11)和 ETHYLENE-RESPONSIVE TRANSCRIPTION FACTOR 1(TaERF1)调节穗发育,但不调节小麦中的 DENSE AND ERECT PANICLE 1(TaDEP1)。水稻中的 SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE 基因 OsSPL14 被认为是理想株型的主要决定因素,其特征为分蘖少、穗粒数多、茎抗倒伏能力强。然而,其在小麦中的同源基因 TaSPL14 的功能尚不清楚。本文报道了 TaSPL14 和 OsSPL14 之间的功能相似性和差异性。与水稻 OsSPL14 敲除体相似,小麦 TaSPL14 敲除植株表现出株高、穗长、小穗数和千粒重降低。但与 OsSPL14 不同的是,TaSPL14 不影响分蘖数。转录组分析表明,与乙烯应答相关的基因在 TaSPL14 敲除系的幼穗中表达显著下调。TaSPL14 可直接结合到乙烯应答基因 TaEIL1、TaRAP2.11 和 TaERF1 的启动子上,并促进其表达,表明 TaSPL14 可能通过乙烯应答途径调节小麦穗发育。阐明 TaSPL14 将有助于理解小麦株型的分子机制。