Sharma K K, Arst H N
Department of Genetics, The University, Newcastle upon Tyne, England.
Curr Genet. 1985;9(4):299-304. doi: 10.1007/BF00419959.
Eight new deletion mutations in the prn gene cluster involved in L-proline catabolism in Aspergillus nidulans have been characterised and mapped. Three of these are located within prnA, the regulatory gene mediating proline induction, and confirm the positive nature of the action of the prnA product. In addition, four prnA- alleles which are phenotypically suppressible by aminoglycoside antibiotics have been identified. Of these four phenotypically suppressible prnA- mutations, two have been tested for suppression by translational suppressors. Both are genotypically suppressible, showing that the prnA product must be a protein.
已对构巢曲霉中参与L-脯氨酸分解代谢的prn基因簇中的8个新缺失突变进行了表征和定位。其中3个位于prnA内,prnA是介导脯氨酸诱导的调控基因,证实了prnA产物作用的阳性性质。此外,还鉴定出4个可被氨基糖苷类抗生素表型抑制的prnA-等位基因。在这4个表型可抑制的prnA-突变中,有2个已通过翻译抑制子进行抑制测试。两者在基因型上均可被抑制,表明prnA产物必定是一种蛋白质。