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严重联合免疫缺陷(scid)小鼠骨髓细胞中异常的免疫球蛋白基因重排

Aberrant immunoglobulin gene rearrangement in scid mouse bone marrow cells.

作者信息

Okazaki K, Nishikawa S, Sakano H

机构信息

Department of Microbiology and Immunology, University of California, Berkeley 94720.

出版信息

J Immunol. 1988 Aug 15;141(4):1348-52.

PMID:3397543
Abstract

We have analyzed Ig gene rearrangement in the immunodeficient mutant mouse, CB-17 scid. Bone marrow stem cells from scid mice were cultured in the in vitro culture system of Whitlock and Witte. Ig gene rearrangement in the scid cells was studied by DNA cloning. Seven DNA clones of Ig H chain JH and DH regions were analyzed by DNA sequencing, and all the clones contained a failure in D-J joining. In the rearranged structure, both DH and JH coding sequences are either partly or completely deleted. Molecular mechanisms causing the aberrant DNA rearrangement are discussed.

摘要

我们分析了免疫缺陷突变小鼠CB-17 scid中的Ig基因重排。从scid小鼠中获取的骨髓干细胞在Whitlock和Witte的体外培养系统中培养。通过DNA克隆研究scid细胞中的Ig基因重排。对7个Ig重链JH和DH区域的DNA克隆进行DNA测序分析,所有克隆均存在D-J连接失败的情况。在重排结构中,DH和JH编码序列部分或完全缺失。文中讨论了导致异常DNA重排的分子机制。

相似文献

1
Aberrant immunoglobulin gene rearrangement in scid mouse bone marrow cells.严重联合免疫缺陷(scid)小鼠骨髓细胞中异常的免疫球蛋白基因重排
J Immunol. 1988 Aug 15;141(4):1348-52.
2
Abnormal recombination of Igh D and J gene segments in transformed pre-B cells of scid mice.重度联合免疫缺陷(scid)小鼠转化前B细胞中Igh D和J基因片段的异常重组。
J Immunol. 1988 Aug 15;141(4):1341-7.
3
Immunoglobulin heavy chain gene diversification in the long-term bone marrow culture of normal mice and mice with severe combined immunodeficiency.正常小鼠和严重联合免疫缺陷小鼠长期骨髓培养中的免疫球蛋白重链基因多样化
Eur J Immunol. 1987 Jul;17(7):1051-7. doi: 10.1002/eji.1830170723.
4
Evidence for defects in V(D)J rearrangements in patients with severe combined immunodeficiency.重症联合免疫缺陷患者V(D)J重排缺陷的证据。
J Immunol. 1994 Jun 1;152(11):5504-13.
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Characterization of B lymphocyte lineage progenitor cells from mice with severe combined immune deficiency disease (SCID) made possible by long term culture.通过长期培养对患有严重联合免疫缺陷病(SCID)的小鼠的B淋巴细胞谱系祖细胞进行鉴定成为可能。
J Immunol. 1987 Apr 15;138(8):2698-705.
6
Secondary rearrangements and post-rearrangement selection contribute to restricted immunoglobulin DJH expression in young rabbit bone marrow.二次重排和重排后选择有助于幼兔骨髓中免疫球蛋白DJH表达受限。
Eur J Immunol. 1995 Mar;25(3):700-7. doi: 10.1002/eji.1830250311.
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Ig heavy chain protein controls B cell development by regulating germ-line transcription and retargeting V(D)J recombination.免疫球蛋白重链蛋白通过调节种系转录和重新靶向V(D)J重组来控制B细胞发育。
J Immunol. 1994 Aug 15;153(4):1645-57.
8
The mouse DNA binding protein Rc for the kappa B motif of transcription and for the V(D)J recombination signal sequences contains composite DNA-protein interaction domains and belongs to a new family of large transcriptional proteins.小鼠DNA结合蛋白Rc,可结合转录的κB基序和V(D)J重组信号序列,它含有复合的DNA-蛋白质相互作用结构域,属于一个新的大型转录蛋白家族。
Genomics. 1996 Aug 1;35(3):415-24. doi: 10.1006/geno.1996.0380.
9
V(D)J recombination generates a high frequency of nonstandard TCR D delta-associated rearrangements in thymocytes.V(D)J重排在胸腺细胞中产生高频的非标准TCR Dδ相关重排。
J Immunol. 1993 Mar 15;150(6):2222-30.
10
Ontogeny of the heavy chain immunoglobulin repertoire in fetal liver and bone marrow.胎儿肝脏和骨髓中重链免疫球蛋白库的个体发生。
J Immunol. 1998 Apr 1;160(7):3274-80.

引用本文的文献

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Efficacy and Safety of Doubly-Regulated Vaccinia Virus in a Mouse Xenograft Model of Multiple Myeloma.双调控痘苗病毒在多发性骨髓瘤小鼠异种移植模型中的疗效与安全性
Mol Ther Oncolytics. 2017 Jul 22;6:57-68. doi: 10.1016/j.omto.2017.07.001. eCollection 2017 Sep 15.
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Defective DNA repair and increased genomic instability in Artemis-deficient murine cells.阿耳忒弥斯缺陷型小鼠细胞中的DNA修复缺陷与基因组不稳定性增加
J Exp Med. 2003 Mar 3;197(5):553-65. doi: 10.1084/jem.20021891.
3
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.
4
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。
Mol Cell Biol. 1993 Jun;13(6):3632-40. doi: 10.1128/mcb.13.6.3632-3640.1993.
5
High frequency of normal DJH joints in B cell progenitors in severe combined immunodeficiency mice.重症联合免疫缺陷小鼠B细胞祖细胞中正常DJH连接的高频率。
J Exp Med. 1993 Sep 1;178(3):1007-16. doi: 10.1084/jem.178.3.1007.
6
The SCID mouse: relevance as an animal model system for studying human disease.重症联合免疫缺陷小鼠:作为研究人类疾病的动物模型系统的相关性。
Am J Pathol. 1993 Dec;143(6):1511-22.
7
Abnormal deletions in the T-cell receptor delta locus of mouse thymocytes.小鼠胸腺细胞T细胞受体δ基因座中的异常缺失。
Mol Cell Biol. 1994 Jul;14(7):4455-64. doi: 10.1128/mcb.14.7.4455-4464.1994.
8
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.
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The mouse mutation severe combined immune deficiency (scid) is on chromosome 16.小鼠突变型严重联合免疫缺陷(scid)位于第16号染色体上。
Immunogenetics. 1989;29(1):54-7. doi: 10.1007/BF02341614.
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Isolation of scid pre-B cells that rearrange kappa light chain genes: formation of normal signal and abnormal coding joins.重排κ轻链基因的scid前B细胞的分离:正常信号和异常编码连接的形成。
EMBO J. 1989 Mar;8(3):735-42. doi: 10.1002/j.1460-2075.1989.tb03433.x.