Brzywczy J, Paszewski A
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, ul. Pawińskiego 5A, 02-106 Warszawa, Poland.
Yeast. 1999 Sep 30;15(13):1403-9. doi: 10.1002/(SICI)1097-0061(19990930)15:13<1403::AID-YEA467>3.0.CO;2-5.
The Kluyveromyces lactis homocysteine synthase gene was cloned by complementation of the Saccharomyces cerevisiae met25 mutation. The coding sequence of the K. lactis gene shows a high similarity to the S. cerevisiae gene. Very little similarity is found in the 5' and 3' untranslated regions. However, one finds short DNA stretches in the promoter of the K. lactis gene which are identical to the nucleotide sequences implicated in the regulation of the S. cerevisiae homologue. This could explain strong transcriptional inhibition of the K. lactis gene by exogenous methionine in the S. cerevisiae host, and indicates a substantial conservation of the sulphur regulatory system between both yeast species.
通过互补酿酒酵母met25突变体克隆了乳酸克鲁维酵母高半胱氨酸合酶基因。乳酸克鲁维酵母基因的编码序列与酿酒酵母基因具有高度相似性。在5'和3'非翻译区发现的相似性非常小。然而,在乳酸克鲁维酵母基因的启动子中发现了短的DNA片段,这些片段与酿酒酵母同源物调控中涉及的核苷酸序列相同。这可以解释在酿酒酵母宿主中外源甲硫氨酸对乳酸克鲁维酵母基因的强烈转录抑制,并表明两种酵母之间硫调节系统有很大的保守性。