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莱茵衣藻中亚硝酸还原酶基因和一个光调节基因与硝酸盐同化位点的聚类。

Clustering of the nitrite reductase gene and a light-regulated gene with nitrate assimilation loci in Chlamydomonas reinhardtii.

作者信息

Quesada A, Gómez I, Fernández E

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Córdoba, Spain.

出版信息

Planta. 1998 Oct;206(2):259-65. doi: 10.1007/s004250050398.

Abstract

Two new loci have been found to be clustered with five other genes for the nitrate assimilation pathway in the Chlamydomonas reinhardtii genome. One gene, located close to the 3'-end of the high-affinity nitrate transporter (HANT) gene Nrt 2; 2, corresponds to the nitrite reductase (NiR) structural gene Nii1. This is supported by a number of experimental findings: (i) NiR-deficient mutants have lost Nii1 gene expression; (ii) Nii1 mRNA accumulation is co-regulated with the expression of other structural genes of the nitrate assimilation pathway; (iii) nitrite (nitrate) utilization ability is recovered in the NiR mutants by functional complementation with a wild-type Nii1 gene; (iv) the elucidated NII1 amino acid sequence is highly similar to that of the cyanobacterial and higher-plant enzyme, and contains the predicted domains for plastidic ferredoxin-NiRs. Thus, the mutant phenotype and the mRNA sequence and expression of the Nii1 gene have been unequivocally related. Accumulation of mRNA for the second locus identified. Lde1 (light-dependent expression), was not regulated by nitrogen, but like nitrate-assimilation clustered genes, its expression was down-regulated in the dark.

摘要

在莱茵衣藻基因组中,已发现两个新的基因座与硝酸盐同化途径的其他五个基因聚集在一起。一个基因位于高亲和力硝酸盐转运蛋白(HANT)基因Nrt 2; 2的3'端附近,对应于亚硝酸还原酶(NiR)结构基因Nii1。这得到了许多实验结果的支持:(i)NiR缺陷型突变体失去了Nii1基因表达;(ii)Nii1 mRNA积累与硝酸盐同化途径的其他结构基因的表达共同调控;(iii)通过与野生型Nii1基因功能互补,NiR突变体恢复了亚硝酸盐(硝酸盐)利用能力;(iv)阐明的NII1氨基酸序列与蓝细菌和高等植物酶的序列高度相似,并包含质体铁氧还蛋白-NiRs的预测结构域。因此,突变体表型与Nii1基因的mRNA序列和表达已明确相关。已鉴定的第二个基因座Lde1(光依赖表达)的mRNA积累不受氮的调节,但与硝酸盐同化聚集基因一样,其表达在黑暗中被下调。

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