IRBV, Biology Department, University of Montreal, Montreal, Canada H1X 2B2.
J Exp Bot. 2013 Apr;64(7):1995-2003. doi: 10.1093/jxb/ert059. Epub 2013 Mar 25.
The stylar determinant of gametophytic self-incompatibility (GSI) in Solanaceae, Rosaceae, and Plantaginaceae is an S-RNase encoded by a multiallelic S-locus. The primary structure of S-RNases shows five conserved (C) and two hypervariable (HV) regions, the latter forming a domain implicated in S-haplotype-specific recognition of the pollen determinant to SI. All S-RNases are glycosylated at a conserved site in the C2 region, although previous studies have shown that N-linked glycans at this position are not required for S-haplotype-specific recognition and pollen rejection. Here the incompatibility phenotype of three constructs derived from an originally monoglycosylated S11-RNase of Solanum chacoense, that were designed to explore the role of the HV domain in determining pollen recognition and the role of the N-linked glycan in the C2 region, is reported. In one series of experiments, a second glycosylation site was introduced in the HVa region to test for inhibition of pollen-specific recognition. This modification does not impede pollen rejection, although analysis shows incomplete glycosylation at the new site in the HVa region. A second construct, designed to permit complete glycosylation at the HVa site by suppression of the conserved site in the C2 region, did increase the degree of site occupancy, but, again, glycosylation was incomplete. Plants expressing this construct rejected S 11 pollen and, surprisingly, also rejected S 13 pollen, thus displaying an unusual dual specificity phenotype. This construct differs from the first by the absence of the conserved C2 glycosylation site, and thus the dual specificity is observed only in the absence of the C2 glycan. A third construct, completely lacking glycosylation sites, conferred an ability to reject only S 11 pollen, disproving the hypothesis that lack of a conserved glycan would confer a universal pollen rejection phenotype to the plant.
茄科、蔷薇科和车前科的配子体自交不亲和性(GSI)的花柱决定因子是由多等位基因 S 基因座编码的 S-RNase。S-RNase 的一级结构显示出五个保守(C)和两个高变(HV)区,后者形成一个结构域,涉及 S 单倍型特异性识别花粉决定因子以实现 SI。所有 S-RNase 在 C2 区的保守位点都被糖基化,尽管先前的研究表明,该位置的 N 连接聚糖对于 S 单倍型特异性识别和花粉排斥并不必需。本研究报道了源自 Solanum chacoense 中单糖基化 S11-RNase 的三个构建体的不亲和表型,这些构建体旨在探索 HV 结构域在决定花粉识别中的作用以及 C2 区中 N 连接聚糖的作用。在一系列实验中,在 HVa 区引入第二个糖基化位点,以测试其对花粉特异性识别的抑制作用。该修饰不会阻碍花粉排斥,尽管分析表明在 HVa 区的新位点存在不完全糖基化。第二个设计用于通过抑制 C2 区的保守位点使 HVa 位点完全糖基化的构建体确实增加了位点占有率,但同样,糖基化不完全。表达该构建体的植物排斥 S11 花粉,并且出人意料地还排斥 S13 花粉,因此表现出异常的双重特异性表型。该构建体与第一个的区别在于缺少保守的 C2 糖基化位点,因此仅在缺乏 C2 聚糖的情况下观察到双重特异性。完全缺乏糖基化位点的第三个构建体仅赋予排斥 S11 花粉的能力,从而否定了缺乏保守聚糖会赋予植物普遍排斥花粉表型的假设。