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酿酒酵母PHO80基因和CEN15的克隆与测序。

Cloning and sequencing of the PHO80 gene and CEN15 of Saccharomyces cerevisiae.

作者信息

Toh-e A, Shimauchi T

机构信息

Department of Fermentation Technology, Hiroshima University, Japan.

出版信息

Yeast. 1986 Jun;2(2):129-39. doi: 10.1002/yea.320020209.

Abstract

The PHO80 gene, which is one of the regulatory genes exerting negative control in the pho system of Saccharomyces cerevisiae, was cloned. The 1.8 kb DNA fragment carrying the PHO80 gene was sequenced and one open reading frame large enough to encode 293 amino acids was found in the sequence. Northern blot analysis of poly(A)+-RNA isolated from cells grown under repressed and derepressed conditions revealed that (i) the size of the PHO80 message was around 1.4 kb, (ii) the expression of the PHO80 gene was not affected by the presence or absence of inorganic phosphate in the medium, and (iii) the expression of the PHO80 gene was not affected by pho2, pho4, pho81, or by pho80 itself. A centromere sequence was found downstream of the PHO80 coding region.

摘要

克隆了酿酒酵母磷酸调节系统中发挥负调控作用的调控基因之一PHO80基因。对携带PHO80基因的1.8 kb DNA片段进行了测序,在该序列中发现了一个足以编码293个氨基酸的开放阅读框。对从处于阻遏和去阻遏条件下生长的细胞中分离的聚腺苷酸(poly(A)+)RNA进行Northern印迹分析,结果显示:(i)PHO80信使RNA的大小约为1.4 kb;(ii)培养基中有无无机磷酸盐不影响PHO80基因的表达;(iii)pho2、pho4、pho81或PHO80自身均不影响PHO80基因的表达。在PHO80编码区下游发现了一个着丝粒序列。

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