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Inactivation of the SR protein splicing factor ASF/SF2 results in genomic instability.SR蛋白剪接因子ASF/SF2的失活会导致基因组不稳定。
Cell. 2005 Aug 12;122(3):365-78. doi: 10.1016/j.cell.2005.06.008.
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Fine-structure analysis of activation-induced deaminase accessibility to class switch region R-loops.活化诱导脱氨酶与类别转换区R环的可及性的精细结构分析。
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An evolutionarily conserved target motif for immunoglobulin class-switch recombination.免疫球蛋白类别转换重组的一个进化保守靶基序。
Nat Immunol. 2004 Dec;5(12):1275-81. doi: 10.1038/ni1137. Epub 2004 Nov 7.
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Evolution of isotype switching.同种型转换的演变
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The hyper IgM syndrome--an evolving story.高IgM综合征——一个不断发展的故事。
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Intracellular transcription of G-rich DNAs induces formation of G-loops, novel structures containing G4 DNA.富含鸟嘌呤的DNA的细胞内转录诱导G-环的形成,G-环是包含G4 DNA的新型结构。
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Class-switch recombination: interplay of transcription, DNA deamination and DNA repair.类别转换重组:转录、DNA脱氨基与DNA修复的相互作用
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Structural basis of transcription: separation of RNA from DNA by RNA polymerase II.转录的结构基础:RNA 聚合酶 II 使 RNA 与 DNA 分离
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9
Nucleic acid structures and enzymes in the immunoglobulin class switch recombination mechanism.免疫球蛋白类别转换重组机制中的核酸结构与酶
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R-loops at immunoglobulin class switch regions in the chromosomes of stimulated B cells.活化B细胞染色体上免疫球蛋白类别转换区的R环。
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小鼠转换区染色体R环的下游边界:对类别转换重组机制的启示

Downstream boundary of chromosomal R-loops at murine switch regions: implications for the mechanism of class switch recombination.

作者信息

Huang Feng-Ting, Yu Kefei, Hsieh Chih-Lin, Lieber Michael R

机构信息

Department of Pathology, University of Southern California Keck School of Medicine, 1441 Eastlake Avenue, MC9176, Los Angeles, CA 90089-9176, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Mar 28;103(13):5030-5. doi: 10.1073/pnas.0506548103. Epub 2006 Mar 17.

DOI:10.1073/pnas.0506548103
PMID:16547142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1458789/
Abstract

R-loops form at Sgamma3 and Sgamma2b Ig class switch regions in the chromosomes of stimulated murine primary B cells and are suspected to be a general feature of mammalian class switch regions. The in vivo upstream boundary of the R-loops is known to begin within the switch repeats. To determine how precisely the R-loop structure conforms to the repetitive zone of the murine Sgamma3 and Sgamma2b switch regions, a chemical probing method was used to obtain structural information on the downstream boundary. We find that only 61-67% of the R-loops terminate within the Sgamma3 and the Sgamma2b repetitive zones, and the remainder terminate downstream, usually within the first 600 bp immediately downstream of the core switch repeats. Interestingly, the nontemplate strand G density falls to the random level gradually through this same region. Hence, the R-loops terminate as the G-richness of the nascent RNA strand falls. This finding is consistent with thermodynamic predictions for RNA:DNA duplex strength relative to that of DNA:DNA duplexes. This result contrasts with the location of known recombination breakpoints, which correlate not with G-richness and R-loop location but rather with AGCT density. The implications of these findings are discussed in the context of models for the targeting of class switch recombination.

摘要

R环在受到刺激的小鼠原代B细胞染色体中的Sgamma3和Sgamma2b Ig类别转换区域形成,并且被怀疑是哺乳动物类别转换区域的一个普遍特征。已知R环在体内的上游边界始于转换重复序列内。为了确定R环结构与小鼠Sgamma3和Sgamma2b转换区域的重复区精确契合的程度,采用了化学探测方法来获取下游边界的结构信息。我们发现,只有61% - 67%的R环在Sgamma3和Sgamma2b重复区内终止,其余的在下游终止,通常在核心转换重复序列下游的前600 bp内。有趣的是,非模板链G密度在同一区域逐渐降至随机水平。因此,随着新生RNA链的富含G程度降低,R环终止。这一发现与RNA:DNA双链相对于DNA:DNA双链强度的热力学预测一致。这一结果与已知重组断点的位置形成对比,已知重组断点与富含G程度和R环位置无关,而是与AGCT密度相关。在类别转换重组靶向模型的背景下讨论了这些发现的意义。