• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Formation of coding joints in V(D)J recombination-inducible severe combined immune deficient pre-B cell lines.V(D)J重组诱导的严重联合免疫缺陷前B细胞系中编码接头的形成
Proc Natl Acad Sci U S A. 1999 Jan 5;96(1):191-6. doi: 10.1073/pnas.96.1.191.
2
Activation of V(D)J recombination induces the formation of interlocus joints and hybrid joints in scid pre-B-cell lines.V(D)J重组的激活在严重联合免疫缺陷前B细胞系中诱导基因座间连接和杂交连接的形成。
Mol Cell Biol. 2000 Oct;20(19):7170-7. doi: 10.1128/MCB.20.19.7170-7177.2000.
3
Signal joint formation is inhibited in murine scid preB cells and fibroblasts in substrates with homopolymeric coding ends.在具有同聚体编码末端的底物中,小鼠严重联合免疫缺陷(scid)前B细胞和成纤维细胞中的信号接头形成受到抑制。
Mol Immunol. 1999 Jun;36(8):551-8. doi: 10.1016/s0161-5890(99)00053-x.
4
The scid recombination-inducible cell line: a model to study DNA-PK-independent V(D)J recombination.严重联合免疫缺陷重组诱导细胞系:一种用于研究不依赖DNA-PK的V(D)J重组的模型。
Immunol Lett. 2000 Dec 1;75(1):21-6. doi: 10.1016/s0165-2478(00)00283-2.
5
Metabolism of recombination coding ends in scid cells.严重联合免疫缺陷(scid)细胞中重组编码末端的代谢
J Immunol. 2000 Apr 15;164(8):4135-42. doi: 10.4049/jimmunol.164.8.4135.
6
A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency.一种对电离辐射敏感性增加且V(D)J重排受损的人类重症联合免疫缺陷(SCID)病症定义了一种新的DNA重组/修复缺陷。
J Exp Med. 1998 Aug 17;188(4):627-34. doi: 10.1084/jem.188.4.627.
7
Formation and resolution of double-strand break intermediates in V(D)J rearrangement.V(D)J重排中双链断裂中间体的形成与解析
Genes Dev. 1995 Oct 1;9(19):2409-20. doi: 10.1101/gad.9.19.2409.
8
Identification of V(D)J recombination coding end intermediates in normal thymocytes.正常胸腺细胞中V(D)J重组编码末端中间体的鉴定。
J Mol Biol. 1997 Mar 21;267(1):1-9. doi: 10.1006/jmbi.1996.0834.
9
Analysis of variable (diversity) joining recombination in DNAdependent protein kinase (DNA-PK)-deficient mice reveals DNA-PK-independent pathways for both signal and coding joint formation.对DNA依赖性蛋白激酶(DNA-PK)缺陷小鼠中可变(多样性)连接重组的分析揭示了信号和编码连接形成的不依赖DNA-PK的途径。
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15559-64. doi: 10.1073/pnas.95.26.15559.
10
Gamma-irradiation directly affects the formation of coding joints in SCID cell lines.γ射线照射直接影响重症联合免疫缺陷(SCID)细胞系中编码接头的形成。
J Immunol. 1999 Nov 15;163(10):5418-26.

引用本文的文献

1
Accessibility of chromosomal recombination breaks in nuclei of wild-type and DNA-PKcs-deficient cells.野生型和DNA-PKcs缺陷型细胞核中染色体重组断裂的可及性。
DNA Repair (Amst). 2009 Jul 4;8(7):813-21. doi: 10.1016/j.dnarep.2009.03.007. Epub 2009 Apr 22.
2
V(D)J recombination in zebrafish: Normal joining products with accumulation of unresolved coding ends and deleted signal ends.斑马鱼中的V(D)J重组:具有未解决的编码末端积累和缺失信号末端的正常连接产物。
Mol Immunol. 2007 Mar;44(7):1793-802. doi: 10.1016/j.molimm.2006.07.295. Epub 2006 Sep 26.
3
Initiation of V(D)J recombination in zebrafish (Danio rerio) ovaries.斑马鱼(Danio rerio)卵巢中V(D)J重组的起始。
Mol Immunol. 2007 Mar;44(7):1784-92. doi: 10.1016/j.molimm.2006.08.012. Epub 2006 Sep 25.
4
Genomic instability due to V(D)J recombination-associated transposition.由于V(D)J重组相关转座导致的基因组不稳定。
Genes Dev. 2006 Jun 15;20(12):1575-82. doi: 10.1101/gad.1432706.
5
Histone 3 lysine 4 methylation during the pre-B to immature B-cell transition.前B细胞向未成熟B细胞转变过程中的组蛋白3赖氨酸4甲基化
Nucleic Acids Res. 2004 Mar 29;32(6):1942-7. doi: 10.1093/nar/gkh523. Print 2004.
6
Role of poly(ADP-ribosyl)ation in DNA-PKcs- independent V(D)J recombination.聚(ADP - 核糖基)化在不依赖DNA - PKcs的V(D)J重组中的作用。
Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4532-7. doi: 10.1073/pnas.072495299.
7
Sensing of intermediates in V(D)J recombination by ATM.ATM对V(D)J重组中间产物的感知。
Genes Dev. 2002 Jan 15;16(2):159-64. doi: 10.1101/gad.956902.
8
Activation of V(D)J recombination induces the formation of interlocus joints and hybrid joints in scid pre-B-cell lines.V(D)J重组的激活在严重联合免疫缺陷前B细胞系中诱导基因座间连接和杂交连接的形成。
Mol Cell Biol. 2000 Oct;20(19):7170-7. doi: 10.1128/MCB.20.19.7170-7177.2000.

本文引用的文献

1
Assembly of a 12/23 paired signal complex: a critical control point in V(D)J recombination.12/23 配对信号复合体的组装:V(D)J 重组中的一个关键控制点。
Mol Cell. 1998 Jun;1(7):1011-9. doi: 10.1016/s1097-2765(00)80101-x.
2
Rejoining of DNA by the RAG1 and RAG2 proteins.由RAG1和RAG2蛋白介导的DNA重新连接。
Science. 1998 Apr 10;280(5361):301-3. doi: 10.1126/science.280.5361.301.
3
Structure of nonhairpin coding-end DNA breaks in cells undergoing V(D)J recombination.正在进行V(D)J重组的细胞中非发夹编码末端DNA断裂的结构。
Mol Cell Biol. 1998 Apr;18(4):2029-37. doi: 10.1128/MCB.18.4.2029.
4
V(D)J recombination: in vitro coding joint formation.V(D)J重排:体外编码连接的形成
Mol Cell Biol. 1997 Nov;17(11):6379-85. doi: 10.1128/MCB.17.11.6379.
5
Coding joint formation in a cell-free V(D)J recombination system.在无细胞V(D)J重组系统中编码关节形成
Immunity. 1997 Aug;7(2):303-14. doi: 10.1016/s1074-7613(00)80532-4.
6
Cell-free V(D)J recombination.无细胞V(D)J重组
Nature. 1997 Jul 31;388(6641):488-91. doi: 10.1038/41351.
7
Nonsense mutation at Tyr-4046 in the DNA-dependent protein kinase catalytic subunit of severe combined immune deficiency mice.重症联合免疫缺陷小鼠的DNA依赖性蛋白激酶催化亚基中Tyr-4046位点的无义突变。
Proc Natl Acad Sci U S A. 1997 Mar 18;94(6):2438-43. doi: 10.1073/pnas.94.6.2438.
8
Characterization of excised DNA intermediates associated with V(D)J recombination at the T-cell receptor delta locus.与T细胞受体δ基因座处V(D)J重组相关的切除DNA中间体的特征分析。
Mol Cell Biol. 1997 May;17(5):2631-41. doi: 10.1128/MCB.17.5.2631.
9
RAG1 and RAG2 form a stable postcleavage synaptic complex with DNA containing signal ends in V(D)J recombination.在V(D)J重组过程中,RAG1和RAG2与含有信号末端的DNA形成稳定的切割后突触复合体。
Cell. 1997 Apr 4;89(1):43-53. doi: 10.1016/s0092-8674(00)80181-6.
10
A complex of RAG-1 and RAG-2 proteins persists on DNA after single-strand cleavage at V(D)J recombination signal sequences.在V(D)J重组信号序列处进行单链切割后,RAG-1和RAG-2蛋白复合物会持续存在于DNA上。
Nucleic Acids Res. 1997 Apr 1;25(7):1375-82. doi: 10.1093/nar/25.7.1375.

V(D)J重组诱导的严重联合免疫缺陷前B细胞系中编码接头的形成

Formation of coding joints in V(D)J recombination-inducible severe combined immune deficient pre-B cell lines.

作者信息

Chang Y, Brown M L

机构信息

Department of Microbiology, Molecular and Cellular Biology Program, Arizona State University, Tempe, AZ 85287-2701, USA.

出版信息

Proc Natl Acad Sci U S A. 1999 Jan 5;96(1):191-6. doi: 10.1073/pnas.96.1.191.

DOI:10.1073/pnas.96.1.191
PMID:9874794
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC15115/
Abstract

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.

摘要

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。