Xu Chuyao, Qi Siyue, Guo Fuchang, Wang Hui, Li Ji, Li Jiazhen, Wu Weilin, Zhou Bo
College of Life Science, Northeast Forestry University, Harbin, China.
Agricultural College, Yanbian University, Yanji, China.
Physiol Plant. 2025 Sep-Oct;177(5):e70471. doi: 10.1111/ppl.70471.
Anthocyanins are crucial compounds known for their antioxidant and health benefits. The Aft tomato (Solanum lycopersicum) line LA1996 can generate anthocyanins in fruits upon light exposure. Despite the identification of various regulatory genes, such as microRNAs and transcription factors involved in anthocyanin biosynthesis across different plant species, the function of the miR156/SPL module in Aft tomato fruit pigmentation is not well understood. In this research, 17 SlSPL family genes of Aft tomato were classified into six clades. SlSPL15 (Solyc10T002263.1) was grouped in Clade V, with AtSPL9, which is known to be involved in anthocyanin biosynthesis in Arabidopsis. Moreover, an inverse relationship between SlSPL15 and miR156a expression in mature green (MG) stage fruits was shown by quantitative RT-PCR analysis. Transient expression analysis of luciferase confirmed that SlSPL15 transcripts are degraded by SlmiR156a. Furthermore, overexpression of SlSPL15 in Aft tomato reduced the anthocyanin accumulation in MG fruits. In SlSPL15 overexpressed tomato plants, the transcription level of SlSPL15 was elevated compared to that in wild-type fruits, whereas the expression of SlPAL, SlCHS1, SlDFR, SlF3H, SlF3'5'H, and SlANS was reduced. Additionally, the expression of light-responsive regulatory genes SlHY5, SlAN2-like, and SlMYB12 in the anthocyanin biosynthetic pathway was also reduced in light-exposed fruits of 35S:SlSPL15 plants. Subcellular localization analysis verified that SlSPL15 is localized in the nucleus, while yeast two-hybrid assays demonstrated its interaction with SlAN2-like, a part of the MBW complex that participates in regulating anthocyanin biosynthesis in Aft tomato fruits. The findings expand our comprehension of the roles of SlSPL15, targeted by SlmiR156a, in regulating light-induced anthocyanin accumulation in tomatoes.
花青素是一类重要的化合物,以其抗氧化作用和对健康的益处而闻名。Aft番茄(Solanum lycopersicum)品系LA1996在光照下果实中能产生花青素。尽管已鉴定出多种调控基因,如参与不同植物物种花青素生物合成的微小RNA和转录因子,但miR156/SPL模块在Aft番茄果实色素沉着中的功能尚不清楚。在本研究中,Aft番茄的17个SlSPL家族基因被分为六个进化枝。SlSPL15(Solyc10T002263.1)被归为进化枝V,与已知参与拟南芥花青素生物合成的AtSPL9在一起。此外,定量RT-PCR分析表明,在绿熟(MG)期果实中,SlSPL15与miR156a的表达呈负相关。荧光素酶瞬时表达分析证实,SlSPL15转录本被SlmiR156a降解。此外,在Aft番茄中过表达SlSPL15会减少MG果实中的花青素积累。在过表达SlSPL15的番茄植株中,与野生型果实相比,SlSPL15的转录水平升高,而SlPAL、SlCHS1、SlDFR、SlF3H、SlF3'5'H和SlANS的表达降低。此外,在35S:SlSPL15植株的光照果实中,花青素生物合成途径中光响应调控基因SlHY5、SlAN2-like和SlMYB12的表达也降低。亚细胞定位分析证实SlSPL15定位于细胞核,而酵母双杂交试验表明它与SlAN2-like相互作用,SlAN2-like是参与调控Aft番茄果实花青素生物合成的MBW复合体的一部分。这些发现扩展了我们对受SlmiR156a靶向的SlSPL15在调控番茄光诱导花青素积累中作用的理解。