Department of Botany, School of Plant Sciences, Plant Science Laboratories, University of Reading Whiteknights, Reading RG6 2AS, United Kingdom.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4340-4. doi: 10.1073/pnas.85.12.4340.
Pollen hydration and self-incompatibility (SI) in Brassica have been studied by using a combination of in vivo video-microscopy and experiments with metabolic inhibitors. Experiments with cycloheximide confirm earlier observations that pollen hydration is regulated through protein synthesis. No protein or glycoprotein has positively been identified with this event; however, it is unlikely that the total pool of any particular glycoprotein is involved, but rather a newly synthesized or otherwise activated fraction. Micromanipulation of pollen on the stigmatic papillae suggests that access to this hydration regulation system is limited to members of the Brassicaceae: pollen grains of other species-even those possessing dry stigmas-fail to hydrate. It is proposed that an interaction between enzymes of the stigma surface and the superficial layer of the pollen grain coating creates continuity between the content of the papillar wall and the grain protoplast. Inhibition of protein synthesis also overcomes SI, and since the advent of regulated hydration and synthesis of the so-called S-gene glycoproteins coincide with the acquisition of the SI system, there is strong circumstantial evidence that the same molecular species is involved in both processes. Experiments with tunicamycin, which prevents glycosylation of glycoproteins, indicate that the glycosyl groups of the S-gene glycoprotein are required for the operation of the SI system but not for the regulation of hydration. Further experiments suggest that pollen is positively inhibited on incompatible papillae but that this inhibition is biostatic. Recovery from the effects of the SI system appears to involve the metabolism of an inhibitor by the pollen. SI in Brassica thus emerges as a sophisticated process under dynamic control in both the female and male partners. The evolutionary advantages of such a system are discussed.
已采用活体视频显微镜与代谢抑制剂实验相结合的方法研究了芸薹属花粉的水合作用和自交不亲和性(SI)。用环己亚胺进行的实验证实了早先的观察结果,即花粉水合作用受蛋白质合成的调节。尚未用该事件鉴定出任何特定的蛋白质或糖蛋白;然而,不太可能涉及任何特定糖蛋白的总池,而是涉及新合成或其他激活的部分。在柱头乳突上对花粉进行微操作表明,对这种水合调节系统的访问仅限于芸薹属的成员:其他物种的花粉粒-即使那些具有干燥柱头的花粉粒-也无法水合。有人提出,柱头表面的酶与花粉粒表面涂层的最外层之间的相互作用在乳突壁的内容物和花粉原生质体之间建立了连续性。蛋白质合成的抑制也克服了 SI,并且由于调节水合作用和所谓 S 基因糖蛋白的合成与 SI 系统的获得同时发生,因此有强有力的间接证据表明同一分子物种参与了这两个过程。用衣霉素进行的实验抑制了糖蛋白的糖基化,表明 S 基因糖蛋白的糖基对 SI 系统的运转是必需的,但对水合作用的调节则不是必需的。进一步的实验表明,花粉在不亲和的乳突上受到阳性抑制,但这种抑制是生物静态的。从 SI 系统的作用中恢复似乎涉及花粉对抑制剂的代谢。因此,芸薹属中的 SI 作为一种在雌性和雄性伴侣中均受动态控制的复杂过程而出现。讨论了这种系统的进化优势。