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一个编码内在膜蛋白的膨压响应基因的发育表达。

Developmental expression of a turgor-responsive gene that encodes an intrinsic membrane protein.

作者信息

Jones J T, Mullet J E

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843, USA.

出版信息

Plant Mol Biol. 1995 Sep;28(6):983-96. doi: 10.1007/BF00032661.

Abstract

We previously reported that the pea (Pisum sativum) gene, Trg31, shows increased transcription and elevated mRNA levels in plant tissues which are dehydrated and lose turgor. The protein encoded by Trg31 is homologous to members of the MIP intrinsic membrane protein superfamily. Expression of Trg31 was characterized during pea seedling development and in transgenic tobacco using Trg31 promoter::Gus fusions. In pea, Trg31 mRNA abundance was highest in roots followed by flowers, stems and leaves. In roots, Trg31 mRNA levels were highest in non-elongating regions and low in root tips. In dark-grown seedlings, Trg31 mRNA levels were high in stems and illumination caused mRNA abundance in stems to decrease. Histochemical analysis of transgenic tobacco expressing Trg31 promoter::Gus constructs showed high GUS activity in root to shoot and hypocotyl to cotyledon junctions and cotyledons in germinating seedlings. High activity was also observed in the leaf marginal meristem and trichomes. In more mature seedlings, Trg31 promoter activity was observed in the non-elongating portion of the root and in stems especially in the vascular tissue. A gradient of expression was noted in leaf to stem junction zones with highest expression in the younger tissues. Very high expression was observed in stems of flowers and other floral tissues including the calyx, corolla, style, ovules, pods and pollen. This expression pattern suggests that the Trg31 gene product may facilitate transport from sources, through transmitting tissues to sinks.

摘要

我们之前报道过,豌豆(Pisum sativum)基因Trg31在脱水并失去膨压的植物组织中表现出转录增加和mRNA水平升高。Trg31编码的蛋白质与MIP内在膜蛋白超家族的成员同源。利用Trg31启动子::Gus融合体对Trg31在豌豆幼苗发育过程中和转基因烟草中的表达进行了表征。在豌豆中,Trg31 mRNA丰度在根中最高,其次是花、茎和叶。在根中,Trg31 mRNA水平在非伸长区域最高,在根尖较低。在黑暗生长的幼苗中,Trg31 mRNA水平在茎中较高,光照导致茎中的mRNA丰度降低。对表达Trg31启动子::Gus构建体的转基因烟草进行组织化学分析,结果显示在发芽幼苗的根到茎、下胚轴到子叶的连接处以及子叶中GUS活性较高。在叶边缘分生组织和毛状体中也观察到高活性。在更成熟的幼苗中,在根的非伸长部分和茎中,特别是在维管组织中观察到Trg31启动子活性。在叶到茎的连接区域注意到表达梯度,在较年轻的组织中表达最高。在花的茎和其他花组织包括花萼、花冠、花柱、胚珠、豆荚和花粉中观察到非常高的表达。这种表达模式表明Trg31基因产物可能促进从源到库,通过传输组织的运输。

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