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罂粟中的自交不亲和性:在不亲和花粉中触发细胞程序性死亡的信号传导

Self-incompatibility in Papaver: signalling to trigger PCD in incompatible pollen.

作者信息

Bosch Maurice, Franklin-Tong Vernonica E

机构信息

School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

J Exp Bot. 2008;59(3):481-90. doi: 10.1093/jxb/erm195. Epub 2007 Sep 14.

Abstract

Sexual reproduction in higher plants uses pollination, involving interactions between pollen and pistil. Self-incompatibility (SI) prevents self-fertilization, providing an important mechanism to promote outbreeding. SI is controlled by the S-locus; discrimination occurs between incompatible pollen, which is rejected, while compatible pollen can achieve fertilization. In Papaver rhoeas, S proteins encoded by the pistil part of the S-locus interact with incompatible pollen to effect rapid inhibition of tip growth. This self-incompatible interaction triggers a Ca(2+)-dependent signalling cascade. SI-specific events triggered in incompatible pollen include rapid depolymerization of the actin cytoskeleton; phosphorylation of soluble inorganic pyrophosphatases, and activation of a MAPK. It has recently been shown that programmed cell death (PCD) is triggered by SI. This provides a precise mechanism for the specific destruction of 'self' pollen. Recent data providing evidence for SI-induced caspase-3-like protease activity, and the involvement of actin depolymerization and MAPK activation in SI-mediated PCD will be discussed. These studies not only significantly advance our understanding of the mechanisms involved in SI, but also contribute to our understanding of functional links between signalling components and initiation of PCD in a plant cell. Recent data demonstrating SI-mediated modification of soluble inorganic pyrophosphatases are also described.

摘要

高等植物中的有性生殖利用授粉过程,这涉及花粉与雌蕊之间的相互作用。自交不亲和性(SI)可防止自花受精,是促进异花授粉的重要机制。SI由S位点控制;不相容的花粉(会被排斥)与相容的花粉之间存在识别差异,其中相容的花粉能够实现受精。在虞美人中,S位点雌蕊部分编码的S蛋白与不相容的花粉相互作用,从而迅速抑制花粉管顶端生长。这种自交不亲和的相互作用会触发一个依赖钙离子的信号级联反应。在不相容花粉中引发的SI特异性事件包括肌动蛋白细胞骨架的快速解聚、可溶性无机焦磷酸酶的磷酸化以及丝裂原活化蛋白激酶(MAPK)的激活。最近的研究表明,程序性细胞死亡(PCD)是由SI触发的。这为特异性破坏“自身”花粉提供了一种精确机制。本文将讨论最近为SI诱导的类半胱天冬酶-3蛋白酶活性提供证据的数据,以及肌动蛋白解聚和MAPK激活在SI介导的PCD中的作用。这些研究不仅极大地推进了我们对SI所涉及机制的理解,也有助于我们理解植物细胞中信号成分与PCD起始之间的功能联系。本文还描述了最近证明SI介导可溶性无机焦磷酸酶修饰的数据。

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