Lee M G, Young R A, Beggs J D
EMBO J. 1984 Dec 1;3(12):2825-30. doi: 10.1002/j.1460-2075.1984.tb02215.x.
The RNA2 gene of Saccharomyces cerevisiae, which has been implicated in splicing the transcripts of nuclear protein coding genes, has been cloned by complementation of the temperature-sensitive growth defect of an rna2-1 mutant strain. The cloned sequence also suppresses the accumulation of unspliced precursor transcripts of the actin gene in an rna2-1 mutant. The gene has been localised to a 3.2-kb DNA restriction fragment and the corresponding low abundance 2.8-kb transcript identified and the 5' ends mapped. Evidence that this cloned sequence represents the RNA2 gene includes homologous integration at the rna2-1 locus and disruption of the RNA2 gene by insertional inactivation. The disrupted allele confers a recessive lethal phenotype, indicating an essential function for the RNA2 gene product.
酿酒酵母的RNA2基因与核蛋白编码基因转录本的剪接有关,通过对rna2 - 1突变株温度敏感生长缺陷的互补作用进行了克隆。克隆的序列还抑制了rna2 - 1突变体中肌动蛋白基因未剪接前体转录本的积累。该基因已定位到一个3.2 kb的DNA限制片段,并鉴定出相应的低丰度2.8 kb转录本,并绘制了其5'端图谱。该克隆序列代表RNA2基因的证据包括在rna2 - 1位点的同源整合以及通过插入失活破坏RNA2基因。破坏的等位基因赋予隐性致死表型,表明RNA2基因产物具有重要功能。