Revers L F, Cardone J M, Bonatto D, Saffi J, Grey M, Feldmann H, Brendel M, Henriques J A P
Depto. de Biofísica/Centro de Biotecnologia-IB-UFRGS, Avenida Bento Gonçalves, 9500, Prédio 43421, Campus do Vale, 91501-907 Porto Alegre, RS, Brazil.
Nucleic Acids Res. 2002 Nov 15;30(22):4993-5003. doi: 10.1093/nar/gkf632.
The conditionally-lethal pso4-1 mutant allele of the spliceosomal-associated PRP19 gene allowed us to study this gene's influence on pre-mRNA processing, DNA repair and sporulation. Phenotypes related to intron-containing genes were correlated to temperature. Splicing reporter systems and RT-PCR showed splicing efficiency in pso4-1 to be inversely correlated to growth temperature. A single amino acid substitution, replacing leucine with serine, was identified within the N-terminal region of the pso4-1 allele and was shown to affect the interacting properties of Pso4-1p. Amongst 24 interacting clones isolated in a two-hybrid screening, seven could be identified as parts of the RAD2, RLF2 and DBR1 genes. RAD2 encodes an endonuclease indispensable for nucleotide excision repair (NER), RLF2 encodes the major subunit of the chromatin assembly factor I, whose deletion results in sensitivity to UVC radiation, while DBR1 encodes the lariat RNA splicing debranching enzyme, which degrades intron lariat structures during splicing. Characterization of mutagen-sensitive phenotypes of rad2Delta, rlf2Delta and pso4-1 single and double mutant strains showed enhanced sensitivity for the rad2Delta pso4-1 and rlf2Delta pso4-1 double mutants, suggesting a functional interference of these proteins in DNA repair processes in Saccharomyces cerevisiae.
剪接体相关PRP19基因的条件致死性pso4 - 1突变等位基因使我们能够研究该基因对前体mRNA加工、DNA修复和孢子形成的影响。与含内含子基因相关的表型与温度相关。剪接报告系统和逆转录聚合酶链反应表明,pso4 - 1中的剪接效率与生长温度呈负相关。在pso4 - 1等位基因的N端区域鉴定出一个单氨基酸取代,丝氨酸取代亮氨酸,并且显示该取代影响Pso4 - 1p的相互作用特性。在双杂交筛选中分离出的24个相互作用克隆中,7个可鉴定为RAD2、RLF2和DBR1基因的部分。RAD2编码核苷酸切除修复(NER)所必需的一种核酸内切酶,RLF2编码染色质组装因子I的主要亚基,其缺失导致对紫外线辐射敏感,而DBR1编码套索状RNA剪接去分支酶,该酶在剪接过程中降解内含子套索结构。rad2Delta、rlf2Delta和pso4 - 1单突变和双突变菌株的诱变敏感表型特征表明,rad2Delta pso4 - 1和rlf2Delta pso4 - 1双突变体具有增强的敏感性,这表明这些蛋白质在酿酒酵母的DNA修复过程中存在功能干扰。