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首页> 外文期刊>The Journal of Horticultural Science & Biotechnology >Response and regulation of the S6PDH gene in apple leaves under osmotic stress.
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Response and regulation of the S6PDH gene in apple leaves under osmotic stress.

机译:渗透胁迫下苹果叶片中 S6PDH 基因的响应与调控。

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Sorbitol is the main product of photosynthesis in members of the Rosaceae family, many of which accumulate sorbitol under osmotic stress. To elucidate whether sorbitol-6-phosphate dehydrogenase (S6PDH; the rate-limiting enzyme for sorbitol synthesis) is involved in the response to osmotic stress and to clarify the mechanism by which expression of the S6PDH gene was induced by drought stress, sorbitol contents, the activity of sorbitol-6-phosphate dehydrogenase, and expression levels of the S6PDH gene were assayed in the leaves of apple (Malus x domestica Borkh. cv. Nagano Fuji) subjected to different intensities of osmotic stress induced by PEG-6000. The results showed that the S6PDH gene was induced by osmotic stress, and the more severe the stress the higher the level of expression of the S6PDH gene. Expression of the S6PDH gene almost coincided with the increases in S6PDH enzyme activity and sorbitol accumulation, suggesting that the S6PDH gene played an important role in the response of apple to osmotic stress. The promoter of the S6PDH gene was isolated using chromosome walking. Analysis of the S6PDH promoter revealed three abscisic acid (ABA)-responsive elements (ABRE), four MYB-recognition sites, and three MYC-binding sites. Deletion analysis of the S6PDH promoter was performed in transgenic tobacco plants. beta -Glucuronidase (GUS) reporter gene activities driven by different fragments of the S6PDH promoter were detected. This work revealed that the key drought and salt-responsive elements of the S6PDH promoter lay in the region between positions -361 and -221. This region of 141 bp contained two ABA-responsive elements and a putative MYB-recognition sequence, and may regulate transcription of the S6PDH gene under osmotic stress.
机译:山梨糖醇是蔷薇科成员光合作用的主要产物,其中许多在渗透胁迫下积累山梨糖醇。阐明山梨醇6-磷酸脱氢酶(S6PDH;山梨糖醇合成的限速酶)是否参与了对渗透胁迫的反应,并阐明了诱导 S6PDH 基因表达的机制通过干旱胁迫,测定了苹果叶片中的山梨醇含量,山梨醇6-磷酸脱氢酶的活性以及 S6PDH 基因的表达水平( Malus x domestica Borkh。cv。Nagano Fuji)受到PEG-6000诱导的不同渗透压强度的影响。结果表明, S6PDH 基因是由渗透胁迫诱导的,胁迫越严重, S6PDH 基因的表达水平就越高。 S6PDH 基因的表达几乎与S6PDH酶活性和山梨醇积累的增加相吻合,表明 S6PDH 基因在苹果对渗透胁迫的响应中起着重要作用。使用染色体行走分离了 S6PDH 基因的启动子。对 S6PDH 启动子的分析显示了三个脱落酸(ABA)反应元件(ABRE),四个MYB识别位点和三个MYC结合位点。在转基因烟草植物中对 S6PDH 启动子进行了缺失分析。检测到由 S6PDH 启动子的不同片段驱动的β-葡萄糖醛酸苷酶(GUS)报告基因活性。这项工作揭示了 S6PDH 启动子的关键干旱和盐响应元件位于-361和-221位之间的区域。 141 bp的区域包含两个ABA响应元件和一个假定的MYB识别序列,并可能在渗透胁迫下调节 S6PDH 基因的转录。

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