de Graaff L, Visser J
Department of Genetics, Agricultural University, Wageningen, The Netherlands.
Curr Genet. 1988 Dec;14(6):553-60. doi: 10.1007/BF00434080.
The complete nucleotide sequence of the Aspergillus nidulans pyruvate kinase gene, including its flanking sequences, is presented. The gene has a 1,578 bp coding sequence that encodes a protein of 526 amino acids; the latter is strongly homologous to the pyruvate kinases found in Saccharomyces cerevisiae (66%) and mammals (53%). The gene is interrupted by seven introns, three of which are in a conserved position compared to those present in the mammalian pyruvate kinase genes sequenced thus far. A fourth intron within the mononucleotide binding fold domain is in a conserved position with respect to the position of an intron within the NAD+ binding region of maize ADH I. The transcription start site has been determined; a major site of transcription was found 80 bp before the translation initiation codon. The promoter region of the A. nidulans pyruvate kinase gene contains no direct homologies with the TATA or CCAAT sequences in the expected region (30-70 bp) before the transcription initiation site. However, extended CT-enriched regions are found in the promotor region, similar to what has been observed in genes that are highly expressed in Saccharomyces cerevisiae and filamentous fungi.
本文给出了构巢曲霉丙酮酸激酶基因的完整核苷酸序列,包括其侧翼序列。该基因有一个1578bp的编码序列,编码一个含526个氨基酸的蛋白质;该蛋白质与酿酒酵母(66%)和哺乳动物(53%)中的丙酮酸激酶高度同源。该基因被7个内含子打断,其中3个与迄今为止测序的哺乳动物丙酮酸激酶基因中的内含子处于保守位置。单核苷酸结合折叠域内的第4个内含子相对于玉米ADH I的NAD+结合区域内的一个内含子的位置处于保守位置。已确定转录起始位点;在翻译起始密码子前80bp处发现一个主要转录位点。构巢曲霉丙酮酸激酶基因的启动子区域在转录起始位点前的预期区域(30 - 70bp)内与TATA或CCAAT序列无直接同源性。然而,在启动子区域发现了富含CT的延伸区域,类似于在酿酒酵母和丝状真菌中高表达的基因中观察到的情况。