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编码酵母多形汉逊酵母中一种Zn(II)2Cys6转录因子的YNA1基因与硝酸盐同化基因YNT1、YNI1和YNR1的聚类,及其在它们转录激活中的作用。

Clustering of the YNA1 gene encoding a Zn(II)2Cys6 transcriptional factor in the yeast Hansenula polymorpha with the nitrate assimilation genes YNT1, YNI1 and YNR1, and its involvement in their transcriptional activation.

作者信息

Avila J, González C, Brito N, Siverio J M

机构信息

Departamento de Bioqu approximately ímica y Biolog approximately ía Molecular, Universidad de La Laguna, E-38206 La Laguna, Tenerife, Canarias, Spain.

出版信息

Biochem J. 1998 Nov 1;335 ( Pt 3)(Pt 3):647-52. doi: 10.1042/bj3350647.

Abstract

The genes encoding the nitrate transporter (YNT1), nitrite reductase (YNI1) and nitrate reductase (YNR1) are clustered in the yeast Hansenula polymorpha. In addition, DNA sequencing of the region containing these genes demonstrated that a new open reading frame called YNA1 (yeast nitrate assimilation) was located between YNR1 and YNI1. The YNA1 gene encodes a protein of 529 residues belonging to the family of Zn(II)2Cys6 fungal transcriptional factors, and has the highest similarity to the transcriptional factors encoded by nirA, and to a smaller extent to nit-4, involved in the nitrate induction of the gene involved in the assimilation of this compound in filamentous fungi. Northern blot analysis showed the presence of the YNA1 transcript in cells incubated in nitrate, nitrate plus ammonium, ammonium, and nitrogen-free media, with a decrease in its levels in those cells incubated in ammonium. In nitrate the strain Deltayna1::URA3, with a disrupted YNA1 gene, neither grew nor expressed the genes YNT1, YNI1 and YNR1. In the gene cluster YNT1-YNI1-YNA1-YNR1, the four genes were transcribed independently in the YNT1-->YNR1 direction and the transcription start sites were determined by primer extension.

摘要

编码硝酸转运蛋白(YNT1)、亚硝酸还原酶(YNI1)和硝酸还原酶(YNR1)的基因在多形汉逊酵母中聚集在一起。此外,对包含这些基因的区域进行DNA测序表明,一个名为YNA1(酵母硝酸盐同化)的新开放阅读框位于YNR1和YNI1之间。YNA1基因编码一个由529个残基组成的蛋白质,属于Zn(II)2Cys6真菌转录因子家族,与nirA编码的转录因子相似度最高,与参与丝状真菌中该化合物同化相关基因的硝酸盐诱导的nit-4相似度较低。Northern印迹分析表明,在硝酸盐、硝酸盐加铵、铵和无氮培养基中培养的细胞中存在YNA1转录本,在铵培养基中培养的细胞中其水平降低。在硝酸盐中,YNA1基因被破坏的Deltayna1::URA3菌株既不生长也不表达YNT1、YNI1和YNR1基因。在基因簇YNT1-YNI1-YNA1-YNR1中,这四个基因在YNT1-->YNR1方向上独立转录,转录起始位点通过引物延伸确定。

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