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苜蓿中一种结节增强型谷氨酰胺合成酶的特性:核苷酸序列、原位定位及转录本分析。

Characterization of a nodule-enhanced glutamine synthetase from alfalfa: nucleotide sequence, in situ localization, and transcript analysis.

作者信息

Temple S J, Heard J, Ganter G, Dunn K, Sengupta-Gopalan C

机构信息

Department of Agronomy and Horticulture, New Mexico State University, Las Cruces 88003, USA.

出版信息

Mol Plant Microbe Interact. 1995 Mar-Apr;8(2):218-27. doi: 10.1094/mpmi-8-0218.

Abstract

We have characterized two glutamine synthetase (GS) cDNA clones (pGS13 and pGS100) representing mRNA from root nodules of alfalfa. pGS13 is a full-length version of a previously isolated partial cDNA from an alfalfa nodule cDNA library, while pGS100 was previously isolated from an alfalfa suspension culture cDNA library. Using the 3' untranslated region of the two cDNAs as gene-specific probes, we have shown that the GS genes represented by pGS100 and pGS13 are expressed in all organs tested, although at varying levels. pGS13, however, represents the nodule-enhanced GS gene class. Genomic Southern blot analysis using gene-specific probes shows multiple hybridizing bands, in each case suggesting multiple genes and/or alleles for each class of cytoplasmic GS genes. In situ hybridization of alfalfa nodule sections with gene-specific antisense RNA probes has shown that the nodule-enhanced GS genes are induced in the invasion zone and that their expression is limited to the symbiotic zone, while the GS genes represented by pGS100 are induced in the early symbiotic zone and are expressed throughout the symbiotic and senescent zones. Transcripts for both sets of GS genes are localized in the infected cells and based on the spatial expression pattern it would appear that the two gene classes are induced independently of the onset of nitrogen fixation.

摘要

我们已鉴定出两个代表苜蓿根瘤中mRNA的谷氨酰胺合成酶(GS)cDNA克隆(pGS13和pGS100)。pGS13是先前从苜蓿根瘤cDNA文库中分离出的部分cDNA的全长版本,而pGS100先前是从苜蓿悬浮培养cDNA文库中分离得到的。使用这两个cDNA的3'非翻译区作为基因特异性探针,我们发现由pGS100和pGS13代表的GS基因在所有测试器官中均有表达,尽管表达水平有所不同。然而,pGS13代表根瘤增强型GS基因类别。使用基因特异性探针进行的基因组Southern印迹分析显示有多个杂交带,每种情况都表明每类细胞质GS基因有多个基因和/或等位基因。用基因特异性反义RNA探针与苜蓿根瘤切片进行原位杂交表明,根瘤增强型GS基因在侵入区被诱导,其表达局限于共生区,而由pGS100代表的GS基因在共生早期区被诱导,并在整个共生区和衰老区表达。两组GS基因的转录本都定位在受感染的细胞中,基于空间表达模式,这两类基因的诱导似乎与固氮作用的开始无关。

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