Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.7.1.2 (nitrate reductase)
 3,861 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Co-suppression of host genes and 35S transgenes encoding nitrate reductase was previously reported in transgenic tobacco plants (Nicotiana tabacum cv. Paraguay or Burley) using either a full-length cDNA or fragments devoid of the 3' and/or 5' UTR. Co-suppression was previously shown to affect a limited fraction of the progeny of one transgenic tobacco line homozygous for a single transgene locus, and the phenomenon occurred at each generation. In this work, 38 combinations of transgene loci derived from 13 independent transgenic lines homozygous for a single transgene locus were field-tested under two different conditions in an attempt to determine the corresponding frequencies of co-suppression, i.e. the percentage of plants showing co-suppression. Each of the 13 homozygous lines exhibited a different frequency of co-suppression, ranging from 0% to 57%. High frequencies were found to be associated with transgene loc carrying a high number of copy of the transgene, suggesting a transgene dose effect. Combinations carrying 2 non-allelic transgene loci in a hemizygous state exhibited frequencies of co-suppression between those of each of the 2 transgene loci in a homozygous state, while combinations carrying 2 non-allelic transgene loci in a homozygous state exhibited frequencies of co-suppression higher than the sum of those of the 2 transgene loci alone in a homozygous state, clearly confirming a transgene dose effect. Co-suppression frequencies were increased when the plants were grown initially in vitro, suggesting some environmental effect. The roles of transgene copy number, number of transgene loci and environmental factors are discussed in the light of a threshold hypothesis.
 ...
PMID:Field trial analysis of nitrate reductase co-suppression: a comparative study of 38 combinations of transgene loci. 757 60

AreA is the principal transcription factor involved in determining nitrogen utilization in Aspergillus nidulans. NH4+ and Gln are utilized preferentially but in their absence, AreA acts to facilitate the expression of genes involved in metabolizing alternative nitrogen sources. It is crucial to the function of AreA that its expression is tightly modulated by the quality and availability of nitrogen sources. One signalling mechanism involves regulated degradation of the areA transcript in response to NH4+ and Gln, which provides the first direct means of monitoring nitrogen signalling in this fungus. Here we assess the specificity of the transcript degradation response, determining that it responds qualitatively to a variety of additional nitrogen sources including Asn. Furthermore, the response to Gln and NH4+ requires the same discrete region of the areA 3'-UTR but both NH4+ and Asn need to be metabolized to Gln before they are effective as a signal. However, NH4+ signalling is independent of AreA activity, unlike Gln and Asn signalling. A mutation in the structural gene for NADP-linked glutamate dehydrogenase, gdhA, which disrupts metabolism of NH4+ to Glu, is additive with mutations in two distinct regions of areA that disrupt the previously identified signalling mechanisms. The triple mutant is both strongly derepressed and expresses very high levels of nitrate reductase activity. These data suggest nitrogen metabolism in A. nidulans is in part regulated in response to the intracellular levels of Gln via the regulated degradation of areA mRNA, but the intracellular Gln level is not the sole determinant of nitrogen metabolite repression.
 ...
PMID:Characterization of nitrogen metabolite signalling in Aspergillus via the regulated degradation of areA mRNA. 1167 84

Nitrate reductase (NR; EC 1.6.1.1-3) can be controlled at both transcriptional and posttranscriptional levels. Here we describe stability of NR mRNA as a mechanism of control. The NR gene in Chlorella vulgaris (Warburg strain) transcribes a stable mRNA and an unstable mRNA. In-vitro-synthesized transcripts representing these mRNAs show the same stability characteristics. The unstable mRNA is 30 nucleotides longer at the 5'-UTR compared to the stable mRNA. Using an RNA-folding program the 5'-UTR of the longer unstable RNA showed a more extensive stem-loop structure compared to the more linear form of the shorter stable mRNA. Transcripts representing RNAs with intermediate 5'-UTRs folded similarly to the long form and were unstable, or similarly to the short form and were more stable. Thus the secondary structure of the 5'-UTR of NR mRNA is important in the stability of NR transcripts in Chlorella and allows the cell to respond to changes in nitrogen source in an energy-efficient manner.
 ...
PMID:The stability of the Chlorella nitrate reductase mRNA is determined by the secondary structure of the 5'-UTR: implications for posttranscriptional regulation of nitrate reductase. 1185 53