Andersen N, Thill G P, Kramer R A
Mol Cell Biol. 1983 Apr;3(4):562-9. doi: 10.1128/mcb.3.4.562-569.1983.
Two EcoRI restriction fragments carrying Saccharomyces cerevisiae repressible acid phosphatase genes were analyzed. Transcripts were mapped by restriction endonuclease cleavage of glyoxal-stabilized R-loops and by gel blot hybridizations to cDNA. Homology between the two fragments was examined by gel blots and heteroduplex analysis. Each fragment carried a region of about 1.5 kilobases that coded for a repressible acid phosphatase, and these regions showed homology to one another. In addition, one fragment carried a second region of somewhat lower homology that probably codes for the so-called constitutive acid phosphatase.
对携带酿酒酵母可阻遏酸性磷酸酶基因的两个EcoRI限制性片段进行了分析。通过对乙二醛稳定的R环进行限制性内切酶切割以及与cDNA进行凝胶印迹杂交来绘制转录本图谱。通过凝胶印迹和异源双链分析检查了两个片段之间的同源性。每个片段都携带一个约1.5千碱基的区域,该区域编码一种可阻遏酸性磷酸酶,并且这些区域彼此显示出同源性。此外,一个片段携带了第二个同源性稍低的区域,该区域可能编码所谓的组成型酸性磷酸酶。