Kronenberger J, Lepingle A, Caboche M, Vaucheret H
Laboratoire de Biologie Cellulaire, INRA, Versailles, France.
Mol Gen Genet. 1993 Jan;236(2-3):203-8. doi: 10.1007/BF00277113.
Three tobacco nitrite reductase (NiR) cDNA clones were isolated using spinach NiR cDNA as a probe. Sequence analysis and Southern blot hybridization revealed four genes in tobacco. Two of these genes presumably derived from the ancestral species Nicotiana tomentosiformis, the other two from the ancestor N. sylvestris. Northern blot analysis showed that one gene from each ancestral genome was expressed predominantly in leaves, whilst RNA from the other was detected mostly in roots. The accumulation of both leaf and root NiR mRNAs was induced by nitrate and repressed by nitrate- or ammonium-derived metabolites. In addition, the expression of the root NiR gene was detectable in leaves of a tobacco nitrate reductase (NR)-deficient mutant. Thus, the regulation of expression of tobacco NiR genes is comparable to the regulation of expression of barley NR genes.
以菠菜亚硝酸还原酶(NiR)cDNA为探针,分离出三个烟草亚硝酸还原酶(NiR)cDNA克隆。序列分析和Southern杂交显示烟草中有四个基因。其中两个基因可能来自祖先种绒毛状烟草,另外两个来自祖先种野生烟草。Northern印迹分析表明,每个祖先基因组中的一个基因主要在叶片中表达,而另一个基因的RNA大多在根中检测到。叶片和根中NiR mRNA的积累均受硝酸盐诱导,并受硝酸盐或铵衍生代谢物的抑制。此外,在烟草硝酸还原酶(NR)缺陷型突变体的叶片中可检测到根NiR基因的表达。因此,烟草NiR基因表达的调控与大麦NR基因表达的调控相似。