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大豆中两个诱导型硝酸还原酶基因对应cDNA克隆的鉴定:野生型和nr1突变体分析

Identification of cDNA clones corresponding to two inducible nitrate reductase genes in soybean: analysis in wild-type and nr1 mutant.

作者信息

Wu S, Lu Q, Kriz A L, Harper J E

机构信息

Department of Agronomy, University of Illinois, Urbana 61801, USA.

出版信息

Plant Mol Biol. 1995 Nov;29(3):491-506. doi: 10.1007/BF00020980.

Abstract

Among higher plants, soybean is unique in that biochemically it has been characterized as having two constitutive nitrate reductase (cNR) isoforms and one substrate-inducible nitrate reductase (iNR) isoform in leaves. All three NR isoforms are expressed in cv. Williams 82 while the nr1 mutant expresses only the iNR isoform. The genetic and molecular mechanisms for regulation of these isoforms have not been elucidated. We describe here the isolation, by reverse transcription-polymerase chain reaction (RT-PCR), of two cDNA clones encoding soybean NR. They were designated as iNR1 and iNR2, respectively, since both were inducible by nitrate. The iNR1 and iNR2 cDNAs cover total encoding regions of 2661 and 2673 nucleotides, respectively. The iNR1 clone shows a 12 bp deletion at the 5' end, relative to iNR2. They show overall similarity of 89% at the nucleotide level, and 87% at the amino acid level. Like all plant NRs cloned so far, deduced amino acid sequences between iNR1 and iNR2 show greatest variation at the N-terminal region while no difference was observed at the C-terminus. Soybean iNR mRNAs were found to be different from those of maize and tobacco in response to tungsten inhibitor treatment, since the inhibitor decreased the steady-state levels of mRNA for soybean iNR and for NiR. Using the same 5' regions of both cDNAs as the probes, Southern blot analysis of genomic DNA revealed differences in organization between iNR1 and iNR2. The genomic DNA from wild-type Williams 82 soybean was shown to have three Eco RI fragments while the nr1 mutant lacked an 8 kb fragment when probed with iNR1 cDNA. Likewise, the nr1 mutant lacked three Hae III restriction fragments when probed with iNR1 cDNA. When probed with iNR2, both wildtype and nr1 mutant showed one identical Eco RI band and two identical Hae III bands. In northern blots, the steady-state level of iNR1 mRNA was similar for the nr1 mutant and the wild-type parent after 20 to 48 h induction by nitrate. Based on the Eco RI and Hae III restriction enzyme digestion patterns observed in Southern blot analysis of soybean DNA, it is concluded that in soybean iNR1 is encoded by a small multiple gene family and iNR2 is a single gene.

摘要

在高等植物中,大豆具有独特之处,从生化角度来看,其叶片中具有两种组成型硝酸还原酶(cNR)同工型和一种底物诱导型硝酸还原酶(iNR)同工型。所有这三种NR同工型都在栽培品种Williams 82中表达,而nr1突变体仅表达iNR同工型。这些同工型的调控遗传和分子机制尚未阐明。我们在此描述了通过逆转录-聚合酶链反应(RT-PCR)分离出两个编码大豆NR的cDNA克隆。它们分别被命名为iNR1和iNR2,因为两者都可被硝酸盐诱导。iNR1和iNR2 cDNA分别覆盖2661和2673个核苷酸的完整编码区域。相对于iNR2,iNR1克隆在5'端有一个12 bp的缺失。它们在核苷酸水平上的总体相似度为89%,在氨基酸水平上为87%。与迄今克隆的所有植物NR一样,iNR1和iNR2之间推导的氨基酸序列在N端区域差异最大,而在C端未观察到差异。发现大豆iNR mRNA在对钨抑制剂处理的反应上与玉米和烟草的不同,因为该抑制剂降低了大豆iNR和NiR的mRNA稳态水平。使用两个cDNA相同的5'区域作为探针,对基因组DNA进行Southern印迹分析揭示了iNR1和iNR2之间在组织上的差异。当用iNR1 cDNA进行探测时,野生型Williams 82大豆的基因组DNA显示有三个Eco RI片段,而nr1突变体缺少一个8 kb的片段。同样,当用iNR1 cDNA进行探测时,nr1突变体缺少三个Hae III限制性片段。当用iNR2进行探测时,野生型和nr1突变体都显示出一条相同的Eco RI带和两条相同的Hae III带。在Northern印迹中,在硝酸盐诱导20至48小时后,nr1突变体和野生型亲本的iNR1 mRNA稳态水平相似。基于在大豆DNA的Southern印迹分析中观察到的Eco RI和Hae III限制性酶切模式,得出结论:在大豆中,iNR1由一个小的多基因家族编码,而iNR2是一个单基因。

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