Lehman C W, Jeong-Yu S, Trautman J K, Carroll D
Department of Biochemistry, University of Utah School of Medicine, Salt Lake City 84132.
Genetics. 1994 Oct;138(2):459-70. doi: 10.1093/genetics/138.2.459.
We have hypothesized that the inheritance of heteroallelic markers during recombination of homologous DNAs in Xenopus oocytes is determined by resolution of a heteroduplex intermediate containing multiple single-base mismatches. To test this idea, we prepared synthetic heteroduplexes carrying 8 separate mispairs in vitro and injected them into oocyte nuclei. DNA was recovered and analyzed directly, by Southern blot-hybridization, and indirectly, by cloning individual repair products in bacteria. Mismatch correction was quite efficient in the oocytes; markers on the same strand were commonly co-corrected, indicating a long-patch mechanism; and the distribution of markers was very similar to that obtained by recombination. This supports our interpretation of the recombination outcome in terms of a resection-annealing mechanism. The injected heteroduplexes carried strand breaks (nicks) as a result of their method of preparation. We tested the idea that mismatch correction might be nick-directed by ligating the strands of the heteroduplex substrate to form covalently closed circles. Repair in oocytes was still efficient, and long patches predominated; but the pattern of recovered markers was quite different than with the nicked substrate. This suggests that nicks, when present, do indeed direct repair, but that, in their absence, recognition of specific mismatches governs repair of the ligated heteroduplexes.
我们推测,非洲爪蟾卵母细胞中同源DNA重组过程中异源等位基因标记的遗传是由包含多个单碱基错配的异源双链中间体的分辨率决定的。为了验证这一想法,我们在体外制备了携带8个单独错配的合成异源双链体,并将它们注入卵母细胞核中。通过Southern印迹杂交直接回收和分析DNA,并通过在细菌中克隆单个修复产物间接进行分析。错配校正在卵母细胞中相当有效;同一条链上的标记通常会共同校正,表明存在长片段机制;并且标记的分布与通过重组获得的分布非常相似。这支持了我们根据切除退火机制对重组结果的解释。由于制备方法的原因,注入的异源双链体带有链断裂(切口)。我们通过连接异源双链体底物的链以形成共价闭合环来测试错配校正可能由切口引导的想法。卵母细胞中的修复仍然有效,并且长片段占主导;但是回收标记的模式与有切口底物的情况有很大不同。这表明,当存在切口时,它们确实会引导修复,但在没有切口的情况下,对特定错配的识别控制着连接的异源双链体的修复。