Chang Y, Brown M L
Department of Microbiology, Molecular and Cellular Biology Program, Arizona State University, Tempe, AZ 85287-2701, USA.
Proc Natl Acad Sci U S A. 1999 Jan 5;96(1):191-6. doi: 10.1073/pnas.96.1.191.
Characterization of the severe combined immune deficient (scid) defect in the recombination process has provided many insights into the underlying mechanisms of variable (diversity) joining recombination. By using recombination-inducible scid pre-B cell lines transformed with the temperature-sensitive Abelson-murine leukemia virus, we show that large quantities of recombination intermediates can be generated, and their resolution can be followed during further cell culture. In this study, we demonstrate that the ability of these scid pre-B cell lines to resolve coding ends depends on the cell culture temperature. At the nonpermissive temperature of 39 degreesC, scid pre-B cell lines fail to form coding joints and contain mostly unresolved hairpin-coding ends. Once the cell culture is returned to the permissive temperature of 33 degreesC, these same cells make a significant amount of coding joints concomitant with the disappearance of hairpin-coding ends. Thus, the scid cells are capable of resolving coding ends under certain culture conditions. However, the majority of the recovered coding joints contains extensive deletions, indicating that the temperature-dependent resolution of coding ends is still scid-like. Our results suggest that the inability of scid cells to promptly nick hairpin-coding ends may lead to aberrant joining in these cells.
对严重联合免疫缺陷(scid)在重组过程中缺陷的特征分析,为深入了解可变(多样)连接重组的潜在机制提供了许多见解。通过使用经温度敏感型阿贝尔逊-鼠白血病病毒转化的重组诱导型scid前B细胞系,我们发现可以产生大量的重组中间体,并且在进一步的细胞培养过程中可以追踪它们的解析情况。在本研究中,我们证明这些scid前B细胞系解析编码末端的能力取决于细胞培养温度。在39℃的非允许温度下,scid前B细胞系无法形成编码接头,并且大多含有未解析的发夹-编码末端。一旦细胞培养恢复到33℃的允许温度,这些相同的细胞会形成大量的编码接头,同时发夹-编码末端消失。因此,scid细胞在某些培养条件下能够解析编码末端。然而,大多数回收的编码接头含有广泛的缺失,这表明编码末端的温度依赖性解析仍然类似scid。我们的结果表明,scid细胞无法迅速切割发夹-编码末端可能导致这些细胞中的异常连接。