Bowater R P, Rosche W A, Jaworski A, Sinden R R, Wells R D
Albert B. Alkek Institute of Biosciences and Technology Texas A and M University Center for Genome Research, Department of Biochemistry and Biophysics Texas Medical Center, Houston 77030, USA.
J Mol Biol. 1996 Nov 22;264(1):82-96. doi: 10.1006/jmbi.1996.0625.
Instabilities that are intrinsic to natural repetitive DNA sequences produce high frequencies of length changes in vivo. Triplet repeats cloned in plasmids in Escherichia coli undergo expansions and deletions, and this instability is affected by multiple factors. We show that CTG-CAG repeats in plasmids can influence the growth of E. coli, which affects the observed stabilities. At extended growth periods, the observed frequencies of deletions were dramatically increased if the cells passed through stationary phase before subculturing. Deletions were particularly pronounced for a plasmid containing the longest repeat, 525 bp in total, with the CTG sequence as the lagging strand template for replication. Measurements of cell growth showed that the lag phase associated with E. coli growth was increased for cultures containing plasmids with long CTG-CAG repeats, particularly when the CTG-containing strand was the lagging template. High frequencies of deletions were observed because of a growth advantage of cells containing plasmids with deleted triplet repeats. Incubation conditions that reduced the bacterial growth-rate produced a decreased extent of deletions, presumably because they alleviated the growth advantage of cells harboring plasmids with deleted triplet repeats. The experimental observations were simulated by a model in which shorter triplet repeats provided a growth advantage due to a shorter lag phase. We demonstrate that the accumulation of deletions within repeating sequences during growth of E. coli can be prevented, and discuss these findings in relation to the studies of repetitive DNA sequences. These are the first observations to show a direct influence between a plasmid-based DNA sequence or structure and factors controlling bacterial growth.
天然重复DNA序列固有的不稳定性在体内产生高频率的长度变化。在大肠杆菌中克隆到质粒中的三联体重复序列会发生扩增和缺失,这种不稳定性受多种因素影响。我们发现质粒中的CTG-CAG重复序列会影响大肠杆菌的生长,进而影响观察到的稳定性。在延长的生长周期中,如果细胞在传代培养前经历了稳定期,观察到的缺失频率会显著增加。对于一个包含最长重复序列(总共525 bp)的质粒,缺失尤为明显,其中CTG序列作为滞后链复制模板。细胞生长测量表明,对于含有长CTG-CAG重复序列质粒的培养物,与大肠杆菌生长相关的滞后阶段会延长,特别是当含CTG的链作为滞后模板时。由于含有缺失三联体重复序列质粒的细胞具有生长优势,因此观察到高频率的缺失。降低细菌生长速率的培养条件导致缺失程度降低,推测是因为它们减轻了含有缺失三联体重复序列质粒的细胞的生长优势。通过一个模型模拟了实验观察结果,在该模型中,较短的三联体重复序列由于滞后阶段较短而具有生长优势。我们证明了在大肠杆菌生长过程中可以防止重复序列内缺失的积累,并结合重复DNA序列的研究讨论了这些发现。这些是首次观察到基于质粒的DNA序列或结构与控制细菌生长的因素之间存在直接影响。