蔗糖转运蛋白转录本的韧皮部移动性和稳定性

Hongxian He, I. Chincinska, A. Hackel, B. Grimm, C. Kühn
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引用次数: 26

摘要

蔗糖转运蛋白是高等植物光合产物分配的重要膜蛋白。在茄属植物中,所有已知的蔗糖转运蛋白都共定位于无核筛元件中,并经历永久的周转。蔗糖转运蛋白StSUT1的mRNA在筛元和伴体细胞中都有定位。蔗糖转运蛋白mrna已在几种植物的韧皮部汁液中被检测到。在此,我们分析了蔗糖转运体转录本在嫁接植物和寄主与寄生植物之间的迁移性。CaMV 35S启动子下表达c-myc标记的无非翻译区(untranslasregions, utr) sut1融合构建体时,发现韧皮部迁移。我们得出结论,3'-和5' - utr都不是mRNA通过胞间连丝运输所必需的。抑制翻译的环己亚胺也会影响SUT转录物的稳定性。当翻译受到抑制时,SUT1转录本会失稳,而SUT2和SUT4转录本在这些条件下累积高达4倍。抑制剂研究揭示了SUT2和SUT4转录物积累的转录后调控。提出了一个解释茄科植物SUT表达协调的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phloem Mobility and Stability of Sucrose Transporter Transcripts
Sucrose transporters are essential membrane proteins for the distribution of photoassimilates in higher plants. In Solanaceous species the proteins of all known sucrose transporters are co-localized in enucleate sieve elements and un- dergo permanent turnover. The mRNA of the sucrose transporter StSUT1 is localized in both, sieve elements and compan- ion cells. Sucrose transporter mRNAs have been detected in the phloem sap of several species. Here, we analyzed the mo- bility of sucrose transporter transcripts in grafted plants and between host and parasitic plants. Phloem-mobility was found when a c-myc tagged SUT1-fusion construct without untranslated regions (UTRs) was expressed under the CaMV 35S promoter. We conclude that neither 3'- nor 5' -UTRs are essential for mRNA transport through plasmodesmata. Cycloheximide, which inhibits translation, has also effects on SUT transcript stability. Whereas SUT1 transcripts are de- stabilized when translation is inhibited, SUT2 and SUT4 transcripts accumulate up to 4fold under these conditions. Inhibi- tor studies revealed post-transcriptional regulation of SUT2 and SUT4 transcript accumulation. A model is proposed ex- plaining the coordination of SUT expression in Solanaceae.
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