Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8572, Japan.
Department of Environmental Horticulture, University of Seoul, 163 Seoulsiripdaero, Dongdaemun-gu, Seoul 02504, Korea.
Plant Cell Physiol. 2022 Oct 31;63(10):1485-1499. doi: 10.1093/pcp/pcac110.
The phenotypic effect of the knockdown/out of AGAMOUS clade MADS-box gene SlMBP3 in tomato was evaluated using a transferred DNA (T-DNA)-tagged mutant of SlMBP3 and SlMBP3-RNA interference lines. SlMBP3 was preferentially expressed in the locular tissue of fruit and the seed coat combined with the endoderm. Consistent with where SlMBP3 is expressed, the SlMBP3-knockout/down lines showed non-liquefied locular tissues and increased number of seed hairs than the wild type (WT). The early cell degradation of the locular tissue was not observed in the fruits of the SlMBP3-knockout/down lines, and the cells were elongated like placental cells resulting in non-liquefied locular tissues. As the result, the fruits of the SlMBP3-knockout/down lines exhibited higher dry matter contents and titratable acidity than those of the WT. During locular tissue cell development under the SlMBP3 knockout/down, the expression of cell-enlargement-related genes (beta-expansin gene SlEXPB1 and endo-beta-1,4-D-glucanase gene Cel8) and pectinase-inhibitor-related genes (pectin esterase inhibitor gene PE inhibitor and polygalacturonase inhibitor gene PG inhibitor) was upregulated and that of pectinase-encoding genes (polygalacturonase gene QRT3-like and pectin lyase gene PL2) was downregulated. In the seed coat of the SlMBP3-knockout/down lines, tomato trichome-formation-related genes such as MYB genes containing R2 and R3 repeats (R2R3-MYB) transcription factor SlMYB75, B-type cyclin SlCycB2 and Homeodomain Leucine Zipper (HD-Zip) IV transcription factor Woolly were downregulated. Our results demonstrate that SlMBP3 is involved in the liquefaction of the locular tissue through the modification of cell development and degradation processes and seed hair formation in tomato fruits, and the SlMBP3 knockout/down results in normal-sized fruit with increased dry matter content.
利用 SlMBP3 的 T-DNA 标签突变体和 SlMBP3-RNAi 系,评估了 AGAMOUS 类 MADS 盒基因 SlMBP3 的敲低/敲除表型效应。SlMBP3 在果实的腔组织和种皮与内胚层结合处优先表达。与 SlMBP3 表达的位置一致,SlMBP3 敲除/敲低系显示出非液化的腔组织和比野生型(WT)更多的种毛。在 SlMBP3 敲除/敲低系的果实中,未观察到腔组织的早期细胞降解,细胞伸长类似于胎盘细胞,导致非液化的腔组织。因此,SlMBP3 敲除/敲低系的果实比 WT 具有更高的干物质含量和可滴定酸度。在 SlMBP3 敲除/敲低条件下的腔组织细胞发育过程中,细胞扩大相关基因(β-扩张蛋白基因 SlEXPB1 和内-β-1,4-D-葡聚糖酶基因 Cel8)和果胶酶抑制剂相关基因(果胶酯酶抑制剂基因 PE 抑制剂和多聚半乳糖醛酸酶抑制剂基因 PG 抑制剂)的表达上调,而果胶酶编码基因(多聚半乳糖醛酸酶基因 QRT3 样和果胶裂解酶基因 PL2)的表达下调。在 SlMBP3 敲除/敲低系的种皮中,番茄毛状体形成相关基因,如含有 R2 和 R3 重复的 R2R3-MYB 转录因子 SlMYB75、B 型细胞周期蛋白 SlCycB2 和同源域亮氨酸拉链(HD-Zip)IV 转录因子 Woolly 的表达下调。我们的结果表明,SlMBP3 通过修饰细胞发育和降解过程以及番茄果实中的种毛形成参与腔组织的液化,SlMBP3 的敲除/敲低导致干物质含量增加的正常大小的果实。