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甜菜V型H⁺-ATP酶亚基A和c亚型的cDNA及基因组克隆:植物发育过程中协同表达及高盐胁迫下协同诱导的证据

cDNA and genomic cloning of sugar beet V-type H+-ATPase subunit A and c isoforms: evidence for coordinate expression during plant development and coordinate induction in response to high salinity.

作者信息

Lehr A, Kirsch M, Viereck R, Schiemann J, Rausch T

机构信息

Botanisches Institut, Universität Heidelberg, Germany.

出版信息

Plant Mol Biol. 1999 Feb;39(3):463-75. doi: 10.1023/a:1006158310891.

Abstract

The plant V-type H+-ATPase (V-ATPase) does not only serve basic housekeeping functions but is also involved in stress-induced NaCl sequestration during salinity stress. To address the question whether the same isoforms conferring housekeeping functions are equally involved in the response to high salinity, we have isolated cDNA clones for subunits A and c, as representing the peripheral V1 complex and the membrane-integral V0 complex, respectively, from the halotolerant sugar beet (Beta vulgaris L., diploid variety). RNA blot analysis with gene-specific probes revealed a coordinate expression of the cloned subunit A and c isoforms during plant development and in response to high salinity. Also, in rapidly dividing suspension-cultured cells with 10-fold increased transcript amounts as compared to young leaf tissue, the ratio of transcripts for both genes was similar to the ratio found for transcripts in leaves of different age. We have then isolated partial genomic clones (BVA/70 for Beta V-ATPase 70 kDa subunit; BVA/16-1 for Beta V-ATPase 16 kDa subunit), including the promoter regions. Transcription start mapping revealed long 5'-UTR leader sequences (230 and 172 bases, respectively) for both genes. Both promoters contain putative G-box motifs in similar distance to the TATA boxes. For a quantitative comparison of relative promoter strength, the BVA/70 and BVA/16-1 promoters linked to the luciferase reporter gene (LUC) were delivered to sugar beet suspension-cultured cells by particle bombardment. The BVA/16-1 promoter showed a 1.7-fold higher activity as compared with the BVA/70 promoter. Salt treatment induced an increase of BVA/70 (+70%) and BVA/16-1 (+57%) promoter activities, concomitant with increased transcript amounts. The following sequences have been deposited at the EMBL database X98767: Beta vulgaris V-ATPase subunit A, cDNA clone; X98851, B. vulgaris V-ATPase subunit c isoform 1, cDNA clone; Y11038, B. vulgaris V-ATPase subunit A, partial genomic clone; Y11037, B. vulgaris V-ATPase subunit c isoform 1, partial genomic clone.

摘要

植物V型H⁺-ATP酶(V-ATP酶)不仅发挥基本的看家功能,还参与盐胁迫期间应激诱导的NaCl隔离。为了解赋予看家功能的相同亚型是否同样参与对高盐度的响应,我们从耐盐甜菜(Beta vulgaris L.,二倍体品种)中分离了亚基A和c的cDNA克隆,分别代表外周V1复合体和膜整合V0复合体。用基因特异性探针进行的RNA印迹分析显示,克隆的亚基A和c亚型在植物发育过程中以及对高盐度的响应中协同表达。此外,在快速分裂的悬浮培养细胞中,与幼叶组织相比转录本量增加了10倍,这两个基因的转录本比例与不同年龄叶片中发现的转录本比例相似。然后我们分离了部分基因组克隆(用于甜菜V-ATP酶70 kDa亚基的BVA/70;用于甜菜V-ATP酶16 kDa亚基的BVA/16-1),包括启动子区域。转录起始定位显示这两个基因都有长的5'-UTR前导序列(分别为230和172个碱基)。两个启动子在与TATA盒相似的距离处都含有推定的G-box基序。为了对相对启动子强度进行定量比较,将与荧光素酶报告基因(LUC)相连的BVA/70和BVA/16-1启动子通过粒子轰击导入甜菜悬浮培养细胞。与BVA/70启动子相比,BVA/16-1启动子的活性高1.7倍。盐处理诱导BVA/70(+70%)和BVA/16-1(+57%)启动子活性增加,同时转录本量也增加。以下序列已存入EMBL数据库:X98767:甜菜V-ATP酶亚基A,cDNA克隆;X98851,甜菜V-ATP酶亚基c亚型1,cDNA克隆;Y11038,甜菜V-ATP酶亚基A,部分基因组克隆;Y11037,甜菜V-ATP酶亚基c亚型1,部分基因组克隆。

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