Oechsner U, Magdolen V, Zoglowek C, Häcker U, Bandlow W
Institute for Genetics and Microbiology, München, FRG.
FEBS Lett. 1988 Dec 19;242(1):187-93. doi: 10.1016/0014-5793(88)81013-5.
Yeast mitochondrial adenylate kinase (high molecular mass form, gene locus: AKY2) is encoded on chromosome IV of the same DNA strand as histone H2A-1. The nontranslated intergenic region spans 560 bp, the nontranscribed spacer can be estimated to comprise at most 300 bp. The TATA-box sequence is contained in a striking environment consisting of 20 alternating pyrimidines and purines. The AKY2 transcript is made constitutively: (i) the cellular mRNA concentration does not vary significantly with either growth conditions or elapse of the cell cycle; (ii) beta-galactosidase activity is about constant in yeast cells grown on various carbon sources after transformation with AKY2-promoter/lacZ fusions; (iii) primer elongation analysis shows that utilization of 5 initiation sites is qualitatively and quantitatively independent of the growth conditions and the carbon source used; (iv) Western blot analysis and adenylate kinase activity measurements indicate the absence of post-transcriptional controls as well.
酵母线粒体腺苷酸激酶(高分子量形式,基因座:AKY2)与组蛋白H2A - 1在同一条DNA链的第四条染色体上编码。非翻译基因间隔区跨度为560 bp,非转录间隔区估计最多包含300 bp。TATA框序列包含在由20个交替的嘧啶和嘌呤组成的显著环境中。AKY2转录本是组成型产生的:(i)细胞mRNA浓度不会随生长条件或细胞周期的推移而显著变化;(ii)在用AKY2启动子/乳糖Z融合体转化后,在各种碳源上生长的酵母细胞中,β - 半乳糖苷酶活性大致恒定;(iii)引物延伸分析表明,5个起始位点的利用在质量和数量上与生长条件和所用碳源无关;(iv)蛋白质印迹分析和腺苷酸激酶活性测量也表明不存在转录后调控。