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差异表达的TPS1基因的两个亚类和具有生化活性的TPS1蛋白可能参与中华猕猴桃的糖信号传导。

Two Subclasses of Differentially Expressed TPS1 Genes and Biochemically Active TPS1 Proteins May Contribute to Sugar Signalling in Kiwifruit Actinidia chinensis.

作者信息

Voogd Charlotte, Brian Lara A, Varkonyi-Gasic Erika

机构信息

The New Zealand Institute for Plant & Food Research Limited (Plant & Food Research) Mt Albert, Auckland Mail Centre, Auckland, New Zealand.

出版信息

PLoS One. 2016 Dec 19;11(12):e0168075. doi: 10.1371/journal.pone.0168075. eCollection 2016.

Abstract

Trehalose metabolism and its intermediate trehalose-6-phosphate (T6P) are implicated in sensing and signalling sucrose availability. Four class I TREHALOSE-6-PHOSPHATE SYNTHASE (TPS1) genes were identified in kiwifruit, three of which have both the TPS and trehalose-6-phosphate phosphatase (TPP) domain, while the fourth gene gives rise to a truncated transcript. The transcript with highest sequence homology to Arabidopsis TPS1, designated TPS1.1a was the most highly abundant TPS1 transcript in all examined kiwifruit tissues. An additional exon giving rise to a small N-terminal extension was found for two of the TPS1 transcripts, designated TPS1.2a and TPS1.2b. Homology in sequence and gene structure with TPS1 genes from Solanaceae suggests they belong to a separate, asterid-specific class I TPS subclade. Expression of full-length and potential splice variants of these two kiwifruit TPS1.2 transcripts was sufficient to substitute for the lack of functional TPS1 in the yeast tps1Δ tps2Δ mutant, but only weak complementation was detected in the yeast tps1Δ mutant, and no or very weak complementation was obtained with the TPS1.1a construct. Transgenic Arabidopsis lines expressing kiwifruit TPS1.2 under the control of 35S promoter exhibited growth and morphological defects. We investigated the responses of plants to elevated kiwifruit TPS1 activity at the transcriptional level, using transient expression of TPS1.2a in Nicotiana benthamiana leaves, followed by RNA-seq. Differentially expressed genes were identified as candidates for future functional analyses.

摘要

海藻糖代谢及其中间产物海藻糖-6-磷酸(T6P)与蔗糖可用性的感知和信号传导有关。在猕猴桃中鉴定出四个I类海藻糖-6-磷酸合酶(TPS1)基因,其中三个同时具有TPS和海藻糖-6-磷酸磷酸酶(TPP)结构域,而第四个基因产生截短的转录本。与拟南芥TPS1序列同源性最高的转录本,命名为TPS1.1a,是所有检测的猕猴桃组织中丰度最高的TPS1转录本。在两个TPS1转录本中发现了一个额外的外显子,导致N端有一个小的延伸,命名为TPS1.2a和TPS1.2b。与茄科TPS1基因在序列和基因结构上的同源性表明它们属于一个单独的、菊类植物特有的I类TPS亚分支。这两个猕猴桃TPS1.2转录本的全长和潜在剪接变体的表达足以替代酵母tps1Δ tps2Δ突变体中功能性TPS1的缺失,但在酵母tps1Δ突变体中仅检测到微弱的互补作用,而TPS1.1a构建体未获得互补作用或仅有非常微弱的互补作用。在35S启动子控制下表达猕猴桃TPS1.2的转基因拟南芥品系表现出生长和形态缺陷。我们利用TPS1.2a在本氏烟草叶片中的瞬时表达,随后进行RNA测序,在转录水平上研究了植物对猕猴桃TPS1活性升高的反应。差异表达基因被鉴定为未来功能分析的候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05ad/5167275/2a9bc52ee98a/pone.0168075.g001.jpg

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