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严重联合免疫缺陷细胞能有效整合发夹状和线性DNA底物。

scid cells efficiently integrate hairpin and linear DNA substrates.

作者信息

Staunton J E, Weaver D T

机构信息

Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts.

出版信息

Mol Cell Biol. 1994 Jun;14(6):3876-83. doi: 10.1128/mcb.14.6.3876-3883.1994.

DOI:10.1128/mcb.14.6.3876-3883.1994
PMID:8196630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358754/
Abstract

The scid mouse mutation affects V(D)J rearrangement and double-strand break repair. scid V(D)J rearrangement is characterized by defective coding joint formation which prevents the development of mature B and T cells. Hairpin DNA has been implicated in the formation of V(D)J coding joints. We found scid cells to be proficient in hairpin processing in the context of DNA integration. In addition, we found that the scid defect did not impair integration of linear DNA via nonhomologous recombination. Therefore, hairpin processing and integration of DNA into the genome are distinct from hypersensitivity to ionizing radiation and the defect in V(D)J recombination.

摘要

严重联合免疫缺陷(scid)小鼠突变影响V(D)J重排和双链断裂修复。scid V(D)J重排的特征是编码接头形成缺陷,这阻止了成熟B细胞和T细胞的发育。发夹DNA与V(D)J编码接头的形成有关。我们发现scid细胞在DNA整合的情况下能够熟练地处理发夹。此外,我们发现scid缺陷并不损害线性DNA通过非同源重组的整合。因此,发夹处理和DNA整合到基因组中与对电离辐射的超敏反应和V(D)J重组缺陷不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f5/358754/6a224b4c7ae5/molcellb00006-0362-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f5/358754/77588ef8fb3a/molcellb00006-0361-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f5/358754/6a224b4c7ae5/molcellb00006-0362-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f5/358754/77588ef8fb3a/molcellb00006-0361-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f5/358754/6a224b4c7ae5/molcellb00006-0362-a.jpg

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1
scid cells efficiently integrate hairpin and linear DNA substrates.严重联合免疫缺陷细胞能有效整合发夹状和线性DNA底物。
Mol Cell Biol. 1994 Jun;14(6):3876-83. doi: 10.1128/mcb.14.6.3876-3883.1994.
2
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Cancer Res. 1995 Apr 15;55(8):1774-9.
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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。
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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.
5
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.
6
Biased T-cell receptor delta element recombination in scid thymocytes.严重联合免疫缺陷(scid)胸腺细胞中存在偏向性的T细胞受体δ链基因重排。
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Characterization of coding ends in thymocytes of scid mice: implications for the mechanism of V(D)J recombination.scid小鼠胸腺细胞中编码末端的特征:对V(D)J重组机制的启示
Immunity. 1995 Jan;2(1):101-12. doi: 10.1016/1074-7613(95)90082-9.
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P nucleotide insertions and the resolution of hairpin DNA structures in mammalian cells.哺乳动物细胞中的P核苷酸插入与发夹DNA结构的解析
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1332-6. doi: 10.1073/pnas.91.4.1332.
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V(D)J recombination: broken DNA molecules with covalently sealed (hairpin) coding ends in scid mouse thymocytes.V(D)J重排:严重联合免疫缺陷(scid)小鼠胸腺细胞中具有共价封闭(发夹)编码末端的断裂DNA分子。
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10
A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p.一个参与DNA双链断裂修复和V(D)J重组的新基因位于人类10号染色体短臂上。
Hum Mol Genet. 2000 Mar 1;9(4):583-8. doi: 10.1093/hmg/9.4.583.

引用本文的文献

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Ku70, an essential gene, modulates the frequency of rAAV-mediated gene targeting in human somatic cells.Ku70是一个必需基因,它可调节人成体细胞中rAAV介导的基因靶向频率。
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DNA hairpin opening mediated by the RAG1 and RAG2 proteins.由RAG1和RAG2蛋白介导的DNA发夹打开。
Mol Cell Biol. 1999 Jun;19(6):4159-66. doi: 10.1128/MCB.19.6.4159.
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DNA-PK is essential only for coding joint formation in V(D)J recombination.DNA依赖蛋白激酶仅对V(D)J重组中编码连接的形成至关重要。

本文引用的文献

1
Quantitative studies of the growth of mouse embryo cells in culture and their development into established lines.对培养的小鼠胚胎细胞生长及其发育成既定细胞系的定量研究。
J Cell Biol. 1963 May;17(2):299-313. doi: 10.1083/jcb.17.2.299.
2
V(D)J recombination coding junction formation without DNA homology: processing of coding termini.不依赖DNA同源性的V(D)J重组编码连接形成:编码末端的加工
Mol Cell Biol. 1993 Nov;13(11):6957-68. doi: 10.1128/mcb.13.11.6957-6968.1993.
3
P nucleotides in V(D)J recombination: a fine-structure analysis.
Nucleic Acids Res. 1998 Sep 1;26(17):3944-8. doi: 10.1093/nar/26.17.3944.
4
Mechanistic constraints on diversity in human V(D)J recombination.人类V(D)J重组多样性的机制性限制
Mol Cell Biol. 1996 Jan;16(1):258-69. doi: 10.1128/MCB.16.1.258.
5
Efficient nonhomologous and homologous recombination in scid cells.scid细胞中高效的非同源和同源重组
Immunogenetics. 1995;42(3):181-7. doi: 10.1007/BF00191223.
6
scid cells are deficient in Ku and replication protein A phosphorylation by the DNA-dependent protein kinase.重症联合免疫缺陷(SCID)细胞中,DNA依赖性蛋白激酶对Ku和复制蛋白A的磷酸化作用存在缺陷。
Mol Cell Biol. 1995 Oct;15(10):5700-6. doi: 10.1128/MCB.15.10.5700.
V(D)J 重组中的 P 核苷酸:精细结构分析
Mol Cell Biol. 1993 Feb;13(2):1078-92. doi: 10.1128/mcb.13.2.1078-1092.1993.
4
Normal V(D)J coding junction formation in DNA ligase I deficiency syndromes.
J Immunol. 1994 Jan 1;152(1):176-83.
5
P nucleotide insertions and the resolution of hairpin DNA structures in mammalian cells.哺乳动物细胞中的P核苷酸插入与发夹DNA结构的解析
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1332-6. doi: 10.1073/pnas.91.4.1332.
6
A severe combined immunodeficiency mutation in the mouse.小鼠中的一种严重联合免疫缺陷突变。
Nature. 1983 Feb 10;301(5900):527-30. doi: 10.1038/301527a0.
7
Enzyme action at 3' termini of ionizing radiation-induced DNA strand breaks.电离辐射诱导的DNA链断裂3'末端的酶促作用。
J Biol Chem. 1983 Dec 25;258(24):15198-205.
8
Patterns of integration of DNA microinjected into cultured mammalian cells: evidence for homologous recombination between injected plasmid DNA molecules.注入培养哺乳动物细胞的DNA整合模式:注入的质粒DNA分子间同源重组的证据
Mol Cell Biol. 1982 Nov;2(11):1372-87. doi: 10.1128/mcb.2.11.1372-1387.1982.
9
The defect in murine severe combined immune deficiency: joining of signal sequences but not coding segments in V(D)J recombination.小鼠严重联合免疫缺陷中的缺陷:V(D)J重组中信号序列的连接而非编码片段的连接。
Cell. 1988 Oct 7;55(1):7-16. doi: 10.1016/0092-8674(88)90004-9.
10
The scid gene encodes a trans-acting factor that mediates the rejoining event of Ig gene rearrangement.scid基因编码一种反式作用因子,该因子介导Ig基因重排的重新连接事件。
Genes Dev. 1988 Jul;2(7):817-29. doi: 10.1101/gad.2.7.817.