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SLPIN1 通过调节生长素外排影响花脱落过程。

SlPIN1 regulates auxin efflux to affect flower abscission process.

机构信息

College of Horticulture, Shenyang Agricultural University, Shenyang, 110866, Liaoning, P. R. China.

Key Laboratory of Protected Horticulture of Ministry of Education, No. 120 Dongling Road, Shenhe District, 110866, P. R. China.

出版信息

Sci Rep. 2017 Nov 2;7(1):14919. doi: 10.1038/s41598-017-15072-7.

DOI:10.1038/s41598-017-15072-7
PMID:29097804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5668252/
Abstract

Solanum lycopersicum PIN-FORMED1 (SlPIN1), a major auxin efflux facilitator, contributes to the establishment of auxin maxima during organ initiation and development in tomato. However, the functions of SlPIN1 during organ abscission remain unclear. In our study, SlPIN1 expression decreased immediately after flower removal and increased following IAA treatment, indicating a high sensitivity to auxin depletion. 1-MCP (an ethylene inhibitor) delayed abscission and down-regulated SlPIN1, indicating that ethylene may positively regulate SlPIN1 and that low expression levels of SlPIN1 may delay abscission. The SlPIN1 protein levels were not consistent with the expression pattern, implying that in addition to transcription, protein degradation also affects SlPIN1 levels during abscission. The phosphorylation of SlPIN1 at Ser418, which significantly declined during abscission, was found to play roles in SlPIN1 localization and auxin transport. We also identified the interaction proteins of SlPIN1, which were involved in phosphorylation and ubiquitylation. Therefore, complex mechanisms mediate SlPIN1 auxin transport capability during abscission. The silencing of SlPIN1 expression accelerated abscission by increasing auxin accumulation in the ovary and decreasing the auxin content in the abscission zone (AZ), indicating that SlPIN1 plays a major role in mediating auxin source-sink transport and the establishment and maintenance of auxin maxima in the AZ.

摘要

番茄中的生长素外排促进因子 SlPIN1(Solanum lycopersicum PIN-FORMED1)在器官起始和发育过程中有助于生长素最大值的建立。然而,SlPIN1 在器官脱落过程中的功能尚不清楚。在我们的研究中,SlPIN1 的表达在去除花后立即下降,并在 IAA 处理后增加,表明对生长素耗竭具有高度敏感性。1-MCP(乙烯抑制剂)延迟了脱落并下调了 SlPIN1,表明乙烯可能正向调节 SlPIN1,而 SlPIN1 的低表达水平可能会延迟脱落。SlPIN1 蛋白水平与表达模式不一致,这意味着除了转录外,蛋白降解也会影响脱落过程中 SlPIN1 的水平。SlPIN1 在丝氨酸 418 处的磷酸化在脱落过程中显著下降,被发现对 SlPIN1 定位和生长素运输起作用。我们还鉴定了 SlPIN1 的相互作用蛋白,它们参与磷酸化和泛素化。因此,复杂的机制介导了 SlPIN1 在脱落过程中的生长素运输能力。沉默 SlPIN1 的表达通过增加子房内生长素的积累和减少离区(AZ)内生长素的含量来加速脱落,表明 SlPIN1 在介导生长素源库运输以及在 AZ 中建立和维持生长素最大值方面起着主要作用。

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