Valone J A, Case M E, Giles N H
Proc Natl Acad Sci U S A. 1971 Jul;68(7):1555-9. doi: 10.1073/pnas.68.7.1555.
In Neurospora crassa, evidence has recently been obtained for a cluster of four closely-linked genes controlling the inducible enzymes catalyzing the first three reactions in the catabolism of quinic acid. Three of these genes appear to be the structural genes for the three enzymes. The fourth gene, designated qa-1, has been interpreted as having a regulatory function, since qa-1 mutants are pleiotropic types, are noninducible for the three enzymes, and form heterocaryons which complement mutants in the structural genes. The present studies were undertaken to elucidate further the nature of the regulatory role of the qa-1 locus. A number of constitutive (qa-1(C)) mutants have been obtained from certain qa-1 mutants as revertants selected for their ability to grow on quinic acid as a sole source of carbon. These qa-1(C) mutants produce high levels of all three enzymes in the absence of an inducer, map within (or very close to) the qa-1 locus, and produce a catabolic dehydroquinase (EC 4.2.1.10) which is indistinguishable, on the basis of thermolability tests, from that of wild type. In addition, when grown in the absence of an inducer, heterocaryons between wild-type (qa-1(+)) and different qa-1(C) mutants exhibit markedly different levels of constitutivity (from 5 to 50% of the particular parental qa-1(C) mutant) for catabolic dehydroquinase, one of the enzymes under qa-1 control. These overall results are interpreted as supporting the hypothesis that the qa-1(+) gene product (presumably a multimeric protein) plays only a positive regulatory role in initiating synthesis of the three quinate catabolic enzymes.
在粗糙脉孢菌中,最近已获得证据表明,有一组四个紧密连锁的基因控制着催化奎尼酸分解代谢前三步反应的诱导酶。其中三个基因似乎是这三种酶的结构基因。第四个基因,命名为qa - 1,被解释为具有调节功能,因为qa - 1突变体是多效性类型,对这三种酶无诱导性,并且形成的异核体可互补结构基因中的突变体。目前的研究旨在进一步阐明qa - 1位点调节作用的本质。从某些qa - 1突变体中获得了一些组成型(qa - 1(C))突变体,这些突变体是因其能够以奎尼酸作为唯一碳源生长而被选作回复体得到的。这些qa - 1(C)突变体在没有诱导剂的情况下会产生高水平的所有三种酶,定位于qa - 1位点内(或非常接近该位点),并且产生一种分解代谢脱氢奎尼酸酶(EC 4.2.1.10),根据热稳定性测试,这种酶与野生型的酶无法区分。此外,当在没有诱导剂的情况下生长时,野生型(qa - 1(+))与不同的qa - 1(C)突变体之间的异核体对于分解代谢脱氢奎尼酸酶(qa - 1控制的酶之一)表现出明显不同的组成型水平(为特定亲本qa - 1(C)突变体的5%至50%)。这些总体结果被解释为支持以下假设:qa - 1(+)基因产物(可能是一种多聚体蛋白)在启动三种奎尼酸分解代谢酶的合成中仅起正调节作用。