Roeder G S, Beard C, Smith M, Keranen S
Mol Cell Biol. 1985 Jul;5(7):1543-53. doi: 10.1128/mcb.5.7.1543-1553.1985.
The his4-917 mutation of Saccharomyces cerevisiae results from the insertion of the Ty element Ty917 into the regulatory region of the HIS4 gene and renders the cell His-. The hist4-912 delta mutant, which carries a solo delta in the 5'-noncoding region of HIS4, is His+ at 37 degrees C but His- at 23 degrees C. Both these mutations interfere with HIS4 expression at the transcriptional level. The His- phenotype of both insertion mutations is suppressed by mutations at the SPT2 locus. The product of the wild-type SPT2 gene apparently represses HIS4 transcription in these mutant strains; this repression is relieved when the SPT2 gene is destroyed by mutation. The repression of transcription by SPT2 presumably results from an interaction between the SPT2+ gene product and Ty or delta sequences. In this paper, we report the cloning and DNA sequence analysis of the wild-type SPT2 gene and show that the gene is capable of encoding a protein of 333 amino acids in length. In addition, we show that a dominant mutation of the SPT2 gene results from the generation of an ochre codon which is presumed to lead to a shortened SPT2 gene product.
酿酒酵母的his4 - 917突变是由于Ty元件Ty917插入到HIS4基因的调控区域所致,使细胞成为组氨酸缺陷型(His-)。hist4 - 912δ突变体在HIS4基因的5'非编码区带有一个单独的δ元件,在37℃时为组氨酸野生型(His+),但在23℃时为组氨酸缺陷型(His-)。这两种突变都在转录水平上干扰HIS4的表达。这两种插入突变的His-表型都被SPT2位点的突变所抑制。野生型SPT2基因的产物显然在这些突变菌株中抑制HIS4转录;当SPT2基因因突变而被破坏时,这种抑制作用就会解除。SPT2对转录的抑制作用可能是由于SPT2+基因产物与Ty或δ序列之间的相互作用。在本文中,我们报道了野生型SPT2基因的克隆和DNA序列分析,并表明该基因能够编码一个长度为333个氨基酸的蛋白质。此外,我们还表明,SPT2基因的一个显性突变是由于产生了一个赭石密码子,推测这会导致SPT2基因产物缩短。