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J Exp Med. 1989 Jun 1;169(6):1903-9. doi: 10.1084/jem.169.6.1903.
2
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7
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8
A genetically determined insertion/deletion related polymorphism in human T cell receptor beta chain (TCRB) includes functional variable gene segments.人类T细胞受体β链(TCRB)中一种由基因决定的插入/缺失相关多态性包含功能性可变基因片段。
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Virus-specific CD8+ T-cell responses in mice transgenic for a T-cell receptor beta chain selected at random.随机选择的T细胞受体β链转基因小鼠中的病毒特异性CD8 + T细胞反应。
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Influence of T-cell receptor genes on chronic experimental autoimmune encephalomyelitis.T细胞受体基因对慢性实验性自身免疫性脑脊髓炎的影响。
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T cell tolerance by clonal elimination in the thymus.胸腺中通过克隆清除实现的T细胞耐受性。
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Murine T-cell receptor mutants with deletions of beta-chain variable region genes.具有β链可变区基因缺失的小鼠T细胞受体突变体。
Proc Natl Acad Sci U S A. 1986 Feb;83(3):767-71. doi: 10.1073/pnas.83.3.767.
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The T cell receptor.T细胞受体。
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The T-cell repertoire is heavily influenced by tolerance to polymorphic self-antigens.T细胞库受到对多态性自身抗原耐受性的严重影响。
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10
Possible role of V beta T cell receptor genes in susceptibility to collagen-induced arthritis in mice.VβT细胞受体基因在小鼠胶原诱导性关节炎易感性中的可能作用。
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RIII S/J(H-2r)。一种近交系小鼠品系,其T细胞受体Vβ基因存在大量缺失。

RIII S/J (H-2r). An inbred mouse strain with a massive deletion of T cell receptor V beta genes.

作者信息

Haqqi T M, Banerjee S, Anderson G D, David C S

机构信息

Department of Immunology, Mayo Clinic, Rochester, Minnesota 55905.

出版信息

J Exp Med. 1989 Jun 1;169(6):1903-9. doi: 10.1084/jem.169.6.1903.

DOI:10.1084/jem.169.6.1903
PMID:2525171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2189337/
Abstract

We have identified an inbred strain of mouse, RIII S/J (H-2r), that has the largest known deletion of the TCR V beta genes by screening with mAb and TCR V beta specific probes. Upon screening of PBL with mAb F23.1, which is specific for V beta 8 TCR, RIII S/J was found to be negative. On further screening with mAb KJ 23a, which is specific for V beta 17a TCR, RIII S/J was completely negative. We next tested RIII S/J with mAb 44-22-1, which is specific for V beta 6 TCR, and found it also to be negative. The (B10 X RIII)F1 mice showed a 50% expression of V beta 6 gene, indicating a genomic rather than a clonal deletion. mAb KJ25, detecting V beta 3, was positive in RIII S/J, denoting the downstream boundary for the deletion. Southern blot analysis of liver DNA using TCR V beta-specific probes confirmed the deletion of V beta 8 gene subfamily and V beta 5 gene subfamily, along with V beta 9, V beta 11, V beta 12, and V beta 13 genes similar to the known TCR V beta deletion mutants (SWR, SJL, C57L, and C57Br). In addition, RIII S/J is missing V beta 6, V beta 15, and V beta 17 genes. Our mapping of the deletion indicates that RIII S/J has lost approximately 130 kb of V beta chromosome and with it 13 V beta genes out of the known 21 V beta genes of the TCR. The deletion is marked by the presence of V beta 10 gene upstream and V beta 3 gene downstream.

摘要

我们通过使用单克隆抗体(mAb)和TCR Vβ特异性探针进行筛选,鉴定出一种近交系小鼠RIII S/J(H-2r),它具有已知最大的TCR Vβ基因缺失。在用对Vβ8 TCR特异的mAb F23.1筛选外周血淋巴细胞(PBL)时,发现RIII S/J呈阴性。在用对Vβ17a TCR特异的mAb KJ 23a进一步筛选时,RIII S/J完全呈阴性。接下来我们用对Vβ6 TCR特异的mAb 44-22-1检测RIII S/J,发现其也呈阴性。(B10×RIII)F1小鼠显示Vβ6基因有50%的表达,表明是基因组缺失而非克隆性缺失。检测Vβ3的mAb KJ25在RIII S/J中呈阳性,表明该缺失的下游边界。使用TCR Vβ特异性探针对肝脏DNA进行Southern印迹分析证实,Vβ8基因亚家族和Vβ5基因亚家族以及Vβ9、Vβ11、Vβ12和Vβ13基因缺失,这与已知的TCR Vβ缺失突变体(SWR、SJL、C57L和C57Br)相似。此外,RIII S/J缺失Vβ6、Vβ15和Vβ17基因。我们对该缺失的定位表明,RIII S/J已丢失约130 kb的Vβ染色体,以及TCR已知的21个Vβ基因中的13个Vβ基因。该缺失以上游的Vβ10基因和下游的Vβ3基因为标志。