IAA-miR164a-NAC100L1模块通过调节胼胝质沉积介导黄瓜/南瓜嫁接苗的共生不相容。

IF 7.6 Q1 GENETICS & HEREDITY 园艺研究(英文) Pub Date : 2023-12-29 eCollection Date: 2024-02-01 DOI:10.1093/hr/uhad287
Mingzhu Yuan, Tong Jin, Jianqiang Wu, Lan Li, Guangling Chen, Jiaqi Chen, Yu Wang, Jin Sun
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引用次数: 0

摘要

嫁接是克服连作障碍、提高作物产量和品质的关键技术之一。然而,砧木与接穗之间的共生不相容性会影响嫁接苗成活后的正常生长发育。目前,嫁接不亲和的具体分子调控机制还很不清楚。本研究发现,IAA-miR164a-NAC100L1模块诱导胼胝质沉积介导黄瓜/南瓜嫁接苗的共生不相容。不相容组合(IG)嫁接界面积累了更多的胼胝质,胼胝质合成酶(CmCalS1)的活性和IAA含量明显高于相容组合(CG)。在 IG 植株根部使用 IAA 极性运输抑制剂会降低 CmCalS 的活性和胼胝质含量。此外,IAA 对 Cm-miR164a 的表达有负向调节作用,Cm-miR164a 可直接定向裂解 CmNAC100L1。有趣的是,CmNAC100L1 与 CmCalS1 相互作用以调节其活性。进一步的分析表明,CmNAC100L1与CmCalS1之间的相互作用提高了IG植株中CmCalS1的活性,但降低了CG植株中CmCalS1的活性。点突变分析表明,CmCalS1蛋白第57位的苏氨酸对维持其在不相容砧木中的酶活性起着关键作用。因此,IAA抑制了Cm-miR164a的表达,从而提高了CmNAC100L1的表达,促进了CmNAC100L1与CmCalS1的相互作用,增强了CmCalS1的活性,导致胼胝质沉积和黄瓜/南瓜嫁接苗的共生不相容。
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IAA-miR164a-NAC100L1 module mediates symbiotic incompatibility of cucumber/pumpkin grafted seedlings through regulating callose deposition.

Grafting is one of the key technologies to overcome the obstacles of continuous cropping, and improve crop yield and quality. However, the symbiotic incompatibility between rootstock and scion affects the normal growth and development of grafted seedlings after survival. The specific molecular regulation mechanism of graft incompatibility is still largely unclear. In this study, we found that the IAA-miR164a-NAC100L1 module induced callose deposition to mediate the symbiotic incompatibility of cucumber/pumpkin grafted seedlings. The incompatible combination (IG) grafting interface accumulated more callose, and the activity of callose synthase (CmCalS1) and IAA content were significantly higher than in the compatible combination (CG). Treatment with IAA polar transport inhibitor in the root of the IG plants decreased CmCalS activity and callose content. Furthermore, IAA negatively regulated the expression of Cm-miR164a, which directly targeted cleavage of CmNAC100L1. Interestingly, CmNAC100L1 interacted with CmCalS1 to regulate its activity. Further analysis showed that the interaction between CmNAC100L1 and CmCalS1 increased the activity of CmCalS1 in the IG plants but decreased it in the CG plants. Point mutation analysis revealed that threonine at the 57th position of CmCalS1 protein played a critical role to maintain its enzyme activity in the incompatible rootstock. Thus, IAA inhibited the expression of Cm-miR164a to elevate the expression of CmNAC100L1, which promoted CmNAC100L1 interaction with CmCalS1 to enhance CmCalS1 activity, resulting in callose deposition and symbiotic incompatibility of cucumber/pumpkin grafted seedlings.

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