Van Vliet-Reedijk J C, Planta R J
Department of Biochemistry and Molecular Biology, Vrije Universiteit, Amsterdam, The Netherlands.
Yeast. 1993 Oct;9(10):1139-47. doi: 10.1002/yea.320091015.
Sequence analysis of a 4 kb fragment from the right arm of Saccharomyces cerevisiae chromosome XI, in combination with Northern hybridization experiments revealed the presence of two genes, designated RHO4a and NUD1. The first gene encodes a 32 kDa protein showing significant sequence similarity with members of the ras family. Its 3'-terminal sequence is virtually identical to a sequence published previously as the RHO4 gene [Matsui and Toh-e, Gene 114 (1992), 43-49], which, however, appears to start at an internal ATG codon. The RHO4a sequence also overlaps the 5'-terminal sequence of the RNC1 gene [Chow et al., Nucl. Acids Res. 20 (1992), 5215-5221] proposed to encode the yeast yNucR endo/exonuclease. The remainder of this RNC1 gene overlaps with the 5'-end of the NUD1 gene. However, the RNC1 sequence lacks a portion of 276 bp that in our fragment is part of the intergenic region separating RHO4a and NUD1. From these results we conclude that the proposed RNC1 gene is the result of a cloning artefact and that the yNucR protein is instead encoded by the NUD1 gene.
对酿酒酵母第十一染色体右臂上一个4kb片段进行序列分析,并结合Northern杂交实验,发现了两个基因,分别命名为RHO4a和NUD1。第一个基因编码一种32kDa的蛋白质,与ras家族成员具有显著的序列相似性。其3'-末端序列与先前发表的作为RHO4基因的序列[Matsui和Toh-e,《基因》114(1992),43-49]几乎相同,然而,该序列似乎从一个内部ATG密码子开始。RHO4a序列也与RNC1基因[Chow等人,《核酸研究》20(1992),5215-5221]的5'-末端序列重叠,该基因被认为编码酵母yNucR内切/外切核酸酶。这个RNC1基因的其余部分与NUD1基因的5'-末端重叠。然而,RNC1序列缺少276bp的一部分,在我们的片段中这部分是分隔RHO4a和NUD1的基因间区域的一部分。从这些结果我们得出结论,所提出的RNC1基因是克隆假象的结果,而yNucR蛋白实际上由NUD1基因编码。