College of Horticulture, State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Nanjing Agricultural University, Nanjing, Jiangsu, China.
The New Zealand Institute for Plant and Food Research Ltd, Mt Albert Research Centre, Auckland, New Zealand.
Plant Biotechnol J. 2023 Jul;21(7):1408-1425. doi: 10.1111/pbi.14046. Epub 2023 Apr 9.
Stone cells are often present in pear fruit, and they can seriously affect the fruit quality when present in large numbers. The plant growth regulator NAA, a synthetic auxin, is known to play an active role in fruit development regulation. However, the genetic mechanisms of NAA regulation of stone cell formation are still unclear. Here, we demonstrated that exogenous application of 200 μM NAA reduced stone cell content and also significantly decreased the expression level of PbrNSC encoding a transcriptional regulator. PbrNSC was shown to bind to an auxin response factor, PbrARF13. Overexpression of PbrARF13 decreased stone cell content in pear fruit and secondary cell wall (SCW) thickness in transgenic Arabidopsis plants. In contrast, knocking down PbrARF13 expression using virus-induced gene silencing had the opposite effect. PbrARF13 was subsequently shown to inhibit PbrNSC expression by directly binding to its promoter, and further to reduce stone cell content. Furthermore, PbrNSC was identified as a positive regulator of PbrMYB132 through analyses of co-expression network of stone cell formation-related genes. PbrMYB132 activated the expression of gene encoding cellulose synthase (PbrCESA4b/7a/8a) and lignin laccase (PbrLAC5) binding to their promotors. As expected, overexpression or knockdown of PbrMYB132 increased or decreased stone cell content in pear fruit and SCW thickness in Arabidopsis transgenic plants. In conclusion, our study shows that the 'PbrARF13-PbrNSC-PbrMYB132' regulatory cascade mediates the biosynthesis of lignin and cellulose in stone cells of pear fruit in response to auxin signals and also provides new insights into plant SCW formation.
石细胞通常存在于梨果实中,当大量存在时,会严重影响果实品质。植物生长调节剂 NAA,一种合成的生长素,已知在果实发育调节中发挥积极作用。然而,NAA 调节石细胞形成的遗传机制尚不清楚。在这里,我们证明了外源应用 200μM 的 NAA 可降低石细胞含量,同时也显著降低了编码转录调节剂 PbrNSC 的表达水平。PbrNSC 被证明与生长素反应因子 PbrARF13 结合。PbrARF13 的过表达降低了梨果实中的石细胞含量和拟南芥转基因植株的次生细胞壁(SCW)厚度。相比之下,利用病毒诱导的基因沉默技术敲低 PbrARF13 的表达则产生相反的效果。PbrARF13 随后被证明通过直接结合其启动子抑制 PbrNSC 的表达,从而进一步降低石细胞含量。此外,通过对与石细胞形成相关基因的共表达网络分析,鉴定 PbrNSC 为 PbrMYB132 的正调控因子。PbrMYB132 通过结合其启动子激活纤维素合酶(PbrCESA4b/7a/8a)和木质素漆酶(PbrLAC5)基因的表达。正如预期的那样,PbrMYB132 的过表达或敲低增加或减少了梨果实中的石细胞含量和拟南芥转基因植株的 SCW 厚度。总之,我们的研究表明,“PbrARF13-PbrNSC-PbrMYB132”调控级联反应介导了梨果实石细胞中木质素和纤维素的生物合成,对生长素信号做出反应,并为植物 SCW 形成提供了新的见解。