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首页> 外文期刊>Molecular and Cellular Biology >nirA, the pathway-specific regulatory gene of nitrate assimilation in Aspergillus nidulans, encodes a putative GAL4-type zinc finger protein and contains four introns in highly conserved regions.
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nirA, the pathway-specific regulatory gene of nitrate assimilation in Aspergillus nidulans, encodes a putative GAL4-type zinc finger protein and contains four introns in highly conserved regions.

机译:nirA,构巢曲霉中硝酸盐同化的途径特异性调控基因,编码一种公认的GAL4型锌指蛋白,并在高度保守的区域含有四个内含子。

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The nucleotide sequence of nirA, mediating nitrate induction in Aspergillus nidulans, has been determined. Alignment of the cDNA and the genomic DNA sequence indicates that the gene contains four introns and encodes a protein of 892 amino acids. The deduced NIRA protein displays all characteristics of a transcriptional activator. A putative double-stranded DNA-binding domain in the amino-terminal part comprises six cysteine residues, characteristic for the GAL4 family of zinc finger proteins. An amino-terminal highly acidic region and two proline-rich regions are also present. The nucleotide sequences of two mutations were determined after they were mapped by transformation with overlapping DNA fragments, amplified by the polymerase chain reaction. nirA87, a mutation conferring noninducibility by nitrate and nitrite, has a -1 frameshift at triplet 340, which eliminates 549 C-terminal amino acids from the polypeptide. Under the assumption that the truncated polypeptide is stable, it comprises the zinc finger domain and the acidic region, which seem not sufficient for transcriptional activation. nirAd-106, an allele conferring nitrogen metabolite derepression of nitrate and nitrite reductase activity, includes two transitions, changing a glutamic acid to a lysine and a valine to an alanine, situated between a basic and a proline-rich region of the protein. Northern (RNA) analysis of the wild type and of constitutive (nirAc) and derepressed (nirAd) mutants show that the nirA transcript does not vary between these strains, being in all cases constitutively expressed. On the other hand, transcript levels of structural genes (niaD and niiA) do vary, being highly inducible in the wild type but constitutively expressed in the nirAc mutant. The nirAd mutant appears phenotypically derepressed, because the niaD and niiA transcript levels are overinduced in the presence of nitrate but are still partially repressed in the presence of ammonium.
机译:已确定了在构巢曲霉中介导硝酸盐诱导的nirA的核苷酸序列。 cDNA与基因组DNA序列的比对表明该基因包含四个内含子,并编码892个氨基酸的蛋白质。推论的NIRA蛋白显示出转录激活因子的所有特征。在氨基末端部分的推定的双链DNA结合结构域包含六个半胱氨酸残基,这是锌指蛋白的GAL4家族的特征。还存在氨基末端的高酸性区域和两个富含脯氨酸的区域。通过用重叠的DNA片段转化定位并通过聚合酶链反应扩增后,确定两个突变的核苷酸序列。 nirA87是一种赋予硝酸盐和亚硝酸盐不可诱导性的突变,在三联体340处有-1移码,从而从多肽中消除了549个C端氨基酸。在截短的多肽是稳定的假设下,它包含锌指结构域和酸性区域,这似乎不足以实现转录激活。 nirAd-106是赋予氮代谢物降低硝酸盐和亚硝酸盐还原酶活性的等位基因,它包括两个转变,将谷氨酸转变为赖氨酸,将缬氨酸转变为丙氨酸,位于蛋白质的碱性和富含脯氨酸的区域之间。对野生型和组成型(nirAc)和去阻遏型(nirAd)突变体的Northern(RNA)分析表明,在所有菌株中,nirA转录本均无差异,在所有情况下都是组成型表达。另一方面,结构基因(niaD和niiA)的转录水平确实有所变化,在野生型中可高度诱导,但在nirAc突变体中组成型表达。 nirAd突变体似乎在表型上受到抑制,因为在硝酸盐存在下niaD和niiA转录水平被过度诱导,但在铵盐存在下仍被部分抑制。

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