Woolford J L, Hereford L M, Rosbash M
Cell. 1979 Dec;18(4):1247-59. doi: 10.1016/0092-8674(79)90236-8.
Yeast mRNA enriched for ribosomal protein mRNA was obtained by isolating poly(A)+ small mRNA from small polysomes. A comparison of cell-free translation of this small mRNA and total mRNA, and electrophoresis of the products on two-dimensional gels which resolve most yeast ribosomal proteins, demonstrated that a 5-10 fold enrichment for ribosomal protein mRNA was obtained. One hundred different recombinant DNA molecules possibly containing ribosomal protein genes were selected by differential colony hybridization of this enriched mRNA and unfractionated mRNA to a bank of yeast pMB9 hybrid plasmids. After screening twenty-five of these candidates, five different clones were found which contain yeast ribosomal protein gene sequences. The yeast mRNAs complementary to these five plasmids code for 35S-methionine-labeled polypeptides which co-migrate on two-dimensional gels with yeast ribosomal proteins. Consistent with previous studies on ribosomal protein mRNAs, the amounts of mRNA complementary to three of these cloned genes are controlled by the RNA2 locus. Although two of the five clones contain more than one yeast gene, none contain more than one identifiable ribosomal protein gene. Thus there is no evidence for "tight" linkage of yeast ribosomal protein genes. Two of the cloned ribosomal protein genes are single-copy genes, whereas two other cloned sequences contain two different copies of the same ribosomal protein gene. The fifth plasmid contains sequences which are repeated in the yeast genome, but it is not known whether any or all of the ribosomal protein gene on this clone contains repetitive DNA.
通过从小型多核糖体中分离聚腺苷酸(poly(A))+ 小mRNA,获得了富含核糖体蛋白mRNA的酵母mRNA。对这种小mRNA和总mRNA的无细胞翻译进行比较,并在能分辨大多数酵母核糖体蛋白的二维凝胶上对产物进行电泳,结果表明核糖体蛋白mRNA得到了5至10倍的富集。通过将这种富集的mRNA和未分级的mRNA与酵母pMB9杂交质粒文库进行差异菌落杂交,选择了100个可能含有核糖体蛋白基因的不同重组DNA分子。在对其中25个候选分子进行筛选后,发现了5个不同的克隆,它们含有酵母核糖体蛋白基因序列。与这5个质粒互补的酵母mRNA编码35S-甲硫氨酸标记的多肽,这些多肽在二维凝胶上与酵母核糖体蛋白共迁移。与先前对核糖体蛋白mRNA的研究一致,与其中三个克隆基因互补的mRNA量受RNA2基因座控制。虽然这5个克隆中有两个包含不止一个酵母基因,但没有一个包含不止一个可识别的核糖体蛋白基因。因此,没有证据表明酵母核糖体蛋白基因存在“紧密”连锁。两个克隆的核糖体蛋白基因是单拷贝基因,而另外两个克隆序列包含同一核糖体蛋白基因的两个不同拷贝。第五个质粒包含在酵母基因组中重复的序列,但尚不清楚该克隆上的任何或所有核糖体蛋白基因是否包含重复DNA。