Denis C L, Malvar T
Department of Biochemistry, University of New Hampshire, Durham 03824.
Genetics. 1990 Feb;124(2):283-91. doi: 10.1093/genetics/124.2.283.
Mutations in the yeast CCR4 gene inhibit expression of the glucose-repressible alcohol dehydrogenase (ADH2), as well as other nonfermentative genes, and suppress increased ADH2 expression caused by the cre1 and cre2 alleles. Both the cre1 and ccr4 alleles were shown to affect ADH II enzyme activity by altering the levels of ADH2 mRNA. Mutations in either CRE1 or CRE2 bypassed the inhibition of ADH2 expression caused by delta insertions at the ADH2 promoter which displace the ADH2 activation sequences 336 bp upstream of the TATA element. These cre1 and cre2 effects were suppressible by the ccr4 allele. The cre1 and ccr4 mutations also affected ADH2 expression when all the ADH2 regulatory sequences upstream of the TATA element were deleted. The relationship of the CRE genes to the SPT genes, which when mutated are capable of bypassing the inhibition of HIS4 expression caused by a delta promoter insertion (his4-912 delta allele), was examined. Both the cre1 and cre2 mutations allowed his4-912 delta expression. ccr4 mutations were able to suppress the ability of the cre alleles to increase his4-912 delta expression. CRE2 was shown to be allelic to the SPT6 gene, and CRE1 was found to be allelic to SPT10. We suggest that the CRE genes comprise a general transcriptional control system in yeast that requires the function of the CCR4 gene.
酵母CCR4基因的突变会抑制葡萄糖可阻遏的乙醇脱氢酶(ADH2)以及其他非发酵基因的表达,并抑制由cre1和cre2等位基因引起的ADH2表达增加。cre1和ccr4等位基因均通过改变ADH2 mRNA的水平来影响ADH II酶的活性。CRE1或CRE2中的突变绕过了由ADH2启动子处的δ插入导致的ADH2表达抑制,该插入将ADH2激活序列取代到TATA元件上游336 bp处。这些cre1和cre2的效应可被ccr4等位基因抑制。当TATA元件上游的所有ADH2调控序列被删除时,cre1和ccr4突变也会影响ADH2的表达。研究了CRE基因与SPT基因的关系,SPT基因发生突变时能够绕过由δ启动子插入(his4-912δ等位基因)引起的HIS4表达抑制。cre1和cre2突变均允许his4-912δ表达。ccr4突变能够抑制cre等位基因增加his4-912δ表达的能力。已证明CRE2与SPT6基因等位,且发现CRE1与SPT10等位。我们认为CRE基因在酵母中构成了一个需要CCR4基因功能的一般转录控制系统。