Wang Jinfang, Zhu Yi, Li Maoying, Zhang Haiying, Zhang Xilong, Tian Shouwei, Ren Yi, Yu Yongtao, Liao Shengjin, Gong Guoyi, Velkov Nikolay, Xu Yong, Zhang Jie
State Key Laboratory of Vegetable Biobreeding, National Engineering Research Center for Vegetables, Beijing Key Laboratory of Crop Molecular Design and Intelligent Breeding, Beijing Key Laboratory of Vegetable Germplasms Improvement, Beijing Vegetable Research Center, Beijing Academy of Agriculture and Forestry Science, Beijing, 100097, China.
China Agricultural University, Beijing, 100193, China.
Plant J. 2025 Jul;123(1):e70292. doi: 10.1111/tpj.70292.
Fruit size correlates with yield potential and serves as a vital agronomic trait. However, the key regulatory genes controlling fruit size in watermelon (Citrullus lanatus) remain poorly understood. In this study, we identified a NAC transcription factor gene ClNAC100 localized to selective sweep regions that positively regulated plant height and fruit size. CRISPR-Cas9-mediated knockout of ClNAC100 caused dramatic reductions in both plant height and fruit size, concomitant with decreased gibberellin (GA) levels in mutants. Exogenous GA application partially rescued the plant height and fruit size of the clnac100 mutant, while it could not restore these traits to wild-type levels. ClNAC100 directly upregulated expansin gene ClEXPA1 and GA biosynthetic genes ClGA3oxs, though DELLA protein interactions attenuated this transcriptional activation. A natural variant (-1087, T/C) of ClNAC100 enabled the Dof transcription factor ClDof4.6 to bind and activate ClNAC100 expression during watermelon domestication. Together, our results demonstrate that ClNAC100 mainly modulates the GA pathway to regulate fruit size and plant height, advancing mechanistic understanding of these agriculturally critical traits.
果实大小与产量潜力相关,是一项重要的农艺性状。然而,控制西瓜(Citrullus lanatus)果实大小的关键调控基因仍知之甚少。在本研究中,我们鉴定出一个定位在选择性清除区域的NAC转录因子基因ClNAC100,它正向调控株高和果实大小。CRISPR-Cas9介导的ClNAC100基因敲除导致突变体的株高和果实大小显著降低,同时突变体中的赤霉素(GA)水平也降低。外源施加GA部分挽救了clnac100突变体的株高和果实大小,但无法将这些性状恢复到野生型水平。ClNAC100直接上调扩张蛋白基因ClEXPA1和GA生物合成基因ClGA3oxs,尽管DELLA蛋白相互作用减弱了这种转录激活。ClNAC100的一个自然变异体(-1087,T/C)使Dof转录因子ClDof4.6在西瓜驯化过程中能够结合并激活ClNAC100的表达。总之,我们的结果表明,ClNAC100主要通过调节GA途径来调控果实大小和株高,增进了对这些农业关键性状的机制理解。