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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Formation of coding joints in V(D)J recombination-inducible severe combined immune deficient pre-B cell lines
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Formation of coding joints in V(D)J recombination-inducible severe combined immune deficient pre-B cell lines

机译:V(D)J重组诱导的严重联合免疫缺陷前B细胞株中编码接头的形成

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摘要

Characterization of the severe combined im- mune deficient (scid) defect in the recombination process has provided many insights into the underlying mechanisms of variable (diversity) joining recombination. By using recom- bination-inducible scid prc-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 39degC, 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 tempera- ture of 33degC, 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 resolu- tion 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.
机译:重组过程中严重的合并免疫缺陷(scid)缺陷的特征为可变(多样性)加入重组的潜在机制提供了许多见识。通过使用对温度敏感的Abelson-鼠白血病病毒转化的重组诱导的scid prc-B细胞系,我们证明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遵循它们的分辨率。在这项研究中,我们证明了这些scid pre-B细胞系解析编码末端的能力取决于细胞培养温度。在39度的非许可温度下,scid pre-B细胞系无法形成编码接头,并且大部分都含有未解析的发夹编码末端。一旦细胞培养物恢复到33℃的允许温度,这些相同的细胞就会形成大量的编码接头,伴随着发夹编码末端的消失。因此,scid细胞能够在某些培养条件下解析编码末端。但是,大多数恢复的编码接头含有大量缺失,表明编码端的温度依赖性分辨率仍然是类似scid的。我们的结果表明,scid细胞无法迅速刻痕发夹编码末端可能会导致这些细胞的异常结合。

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