College of Horticulture, Qingdao Agricultural University, Qingdao 266109, China.
Int J Mol Sci. 2024 Jul 24;25(15):8080. doi: 10.3390/ijms25158080.
Cuttage is the main propagation method of tea plant cultivars in China. However, some tea softwood cuttings just form an expanded and loose callus at the base, without adventitious root (AR) formation during the propagation period. Meanwhile, exogenous auxin could promote the AR formation of tea plant cuttings, but the regulation mechanism has not yet explained clearly. We conducted this study to elucidate the regulatory mechanism of exogenous auxin-induced adventitious root (AR) formation of such cuttings. The transcriptional expression profile of non-rooting tea calluses in response to exogenous IBA and NAA was analyzed using ONT RNA Seq technology. In total, 56,178 differentially expressed genes (DEGs) were detected, and most of genes were significantly differentially expressed after 12 h of exogenous auxin treatment. Among these DEGs, we further identified 80 DEGs involved in the auxin induction pathway and AR formation. Specifically, 14 auxin respective genes (ARFs, GH3s, and AUX/IAAs), 3 auxin transporters (AUX22), 19 auxin synthesis- and homeostasis-related genes (cytochrome P450 (CYP450) and calmodulin-like protein (CML) genes), and 44 transcription factors (LOB domain-containing protein (LBDs), SCARECROW-LIKE (SCL), zinc finger protein, WRKY, MYB, and NAC) were identified from these DEGs. Moreover, we found most of these DEGs were highly up-regulated at some stage before AR formation, suggesting that they may play a potential role in the AR formation of tea plant cuttings. In summary, this study will provide a theoretical foundation to deepen our understanding of the molecular mechanism of AR formation in tea cuttings induced by auxin during propagation time.
扦插是中国茶树品种主要的繁殖方法。然而,一些茶树嫩枝扦插在繁殖期间仅在基部形成扩展和疏松的愈伤组织,而没有不定根(AR)形成。同时,外源生长素可以促进茶树插条的不定根形成,但调节机制尚未得到清晰解释。本研究旨在阐明外源生长素诱导茶树插条不定根形成的调节机制。我们使用 ONT RNA Seq 技术分析了对非生根茶树愈伤组织对外源 IBA 和 NAA 响应的转录表达谱。共检测到 56178 个差异表达基因(DEGs),大多数基因在外源激素处理 12 小时后表达显著差异。在这些 DEGs 中,我们进一步鉴定了 80 个参与生长素诱导途径和不定根形成的 DEGs。具体而言,14 个生长素相关基因(ARFs、GH3s 和 AUX/IAAs)、3 个生长素转运蛋白(AUX22)、19 个生长素合成和稳态相关基因(细胞色素 P450(CYP450)和钙调素样蛋白(CML)基因)和 44 个转录因子(富含 LOB 结构域的蛋白(LBDs)、SCARECROW-LIKE(SCL)、锌指蛋白、WRKY、MYB 和 NAC)从这些 DEGs 中鉴定出来。此外,我们发现这些 DEGs 中的大多数在 AR 形成之前的某个阶段高度上调,这表明它们可能在茶树插条的不定根形成中发挥潜在作用。总之,本研究将为加深我们对生长素诱导茶树插条不定根形成分子机制的理解提供理论基础。