Pulak R A, Anderson P
Department of Genetics, University of Wisconsin, Madison 53706.
Mol Cell Biol. 1988 Sep;8(9):3748-54. doi: 10.1128/mcb.8.9.3748-3754.1988.
We have investigated the structural features of spontaneous deletions in Caenorhabditis elegans. We cloned and sequenced the junctions of 16 spontaneous deletions affecting the unc-54 myosin heavy-chain gene and compared their sequences with those of the wild type. We analyzed these sequences in an attempt to identify structural features of the gene that are consistently involved in the spontaneous deletion process. Most deletions (15 of 16) removed a single contiguous region of DNA, with no nucleotides inserted or rearranged at the deletion junctions; one deletion was more complex. unc-54 deletions were small, averaging 600 base pairs in length, and were randomly distributed throughout the gene. Unlike deletions that occur in Escherichia coli, spontaneous unc-54 deletions did not contain statistically significant direct or inverted repeats at or near their termini. Except for their small average size, we have not identified any distinguishing features of their sequence or structure. We discuss these results with regard to the mechanisms for spontaneous deletion in eucaryotic and procaryotic cells.
我们研究了秀丽隐杆线虫自发缺失的结构特征。我们克隆并测序了16个影响unc-54肌球蛋白重链基因的自发缺失的连接点,并将它们的序列与野生型序列进行了比较。我们分析这些序列,试图确定该基因中始终参与自发缺失过程的结构特征。大多数缺失(16个中的15个)去除了一段连续的DNA区域,在缺失连接点处没有核苷酸插入或重排;有一个缺失更为复杂。unc-54缺失很小,平均长度为600个碱基对,并且随机分布在整个基因中。与大肠杆菌中发生的缺失不同,自发的unc-54缺失在其末端或附近不包含具有统计学意义的正向或反向重复序列。除了它们平均尺寸较小外,我们尚未确定其序列或结构的任何显著特征。我们就真核细胞和原核细胞中自发缺失的机制讨论了这些结果。