Paulovich A G, Thompson J R, Larkin J C, Li Z, Woolford J L
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213.
Genetics. 1993 Nov;135(3):719-30. doi: 10.1093/genetics/135.3.719.
The Saccharomyces cerevisiae CRY1 gene encodes the 40S ribosomal subunit protein rp59 and confers sensitivity to the protein synthesis inhibitor cryptopleurine. A yeast strain containing the cry1-delta 1::URA3 null allele is viable, cryptopleurine sensitive (CryS), and expresses rp59 mRNA, suggesting that there is a second functional CRY gene. The CRY2 gene has been isolated from a yeast genomic library cloned in bacteriophage lambda, using a CRY1 DNA probe. The DNA sequence of the CRY2 gene contains an open reading frame encoding ribosomal protein 59 that differs at five residues from rp59 encoded by the CRY1 gene. The CRY2 gene was mapped to the left arm of chromosome X, centromere-proximal to cdc6 and immediately adjacent to ribosomal protein genes RPS24A and RPL46. Ribosomal protein 59 is an essential protein; upon sporulation of a diploid doubly heterozygous for cry1-delta 2::TRP1 cry2-delta 1::LEU2 null alleles, no spore clones containing both null alleles were recovered. Several results indicate that CRY2 is expressed, but at lower levels than CRY1: (1) Introduction of CRY2 on high copy plasmids into CryR yeast of genotype cry1 CRY2 confers a CryS phenotype. Transformation of these CryR yeast with CRY2 on a low copy CEN plasmid does not confer a CryS phenotype. (2) Haploids containing the cry1-delta 2::TRP1 null allele have a deficit of 40S ribosomal subunits, but cry2-delta 1::LEU2 strains have wild-type amounts of 40S ribosomal subunits. (3) CRY2 mRNA is present at lower levels than CRY1 mRNA. (4) Higher levels of beta-galactosidase are expressed from a CRY1-lacZ gene fusion than from a CRY2-lacZ gene fusion. Mutations that alter or eliminate the last amino acid of rp59 encoded by either CRY1 or CRY2 result in resistance to cryptopleurine. Because CRY2 (and cry2) is expressed at lower levels than CRY1 (and cry1), the CryR phenotype of cry2 mutants is only expressed in strains containing a cry1-delta null allele.
酿酒酵母CRY1基因编码40S核糖体亚基蛋白rp59,并赋予对蛋白质合成抑制剂隐丹参酮的敏感性。含有cry1 - delta 1::URA3无效等位基因的酵母菌株是有活力的,对隐丹参酮敏感(CryS),并表达rp59 mRNA,这表明存在第二个功能性CRY基因。使用CRY1 DNA探针,从克隆在噬菌体λ中的酵母基因组文库中分离出CRY2基因。CRY2基因的DNA序列包含一个编码核糖体蛋白59的开放阅读框,该蛋白与CRY1基因编码的rp59在五个残基上不同。CRY2基因被定位到X染色体的左臂,着丝粒近端为cdc6,紧邻核糖体蛋白基因RPS24A和RPL46。核糖体蛋白59是一种必需蛋白;对于cry1 - delta 2::TRP1 cry2 - delta 1::LEU2无效等位基因的二倍体双杂合子进行孢子形成时,没有回收同时包含两个无效等位基因的孢子克隆。几个结果表明CRY2被表达,但表达水平低于CRY1:(1)将高拷贝质粒上的CRY2导入基因型为cry1 CRY2的CryR酵母中会赋予CryS表型。用低拷贝CEN质粒上的CRY2转化这些CryR酵母不会赋予CryS表型。(2)含有cry1 - delta 2::TRP1无效等位基因的单倍体40S核糖体亚基有缺陷,但cry2 - delta 1::LEU2菌株的40S核糖体亚基数量为野生型。(3)CRY2 mRNA的水平低于CRY1 mRNA。(4)从CRY1 - lacZ基因融合体表达的β - 半乳糖苷酶水平高于从CRY2 - lacZ基因融合体表达的水平。改变或消除由CRY1或CRY2编码的rp59的最后一个氨基酸的突变会导致对隐丹参酮产生抗性。因为CRY2(和cry2)的表达水平低于CRY1(和cry1),cry2突变体的CryR表型仅在含有cry1 - delta无效等位基因的菌株中表达。