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本文引用的文献

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Reduced level of the BCL11B protein is associated with adult T-cell leukemia/lymphoma.BCL11B 蛋白水平降低与成人 T 细胞白血病/淋巴瘤相关。
PLoS One. 2013;8(1):e55147. doi: 10.1371/journal.pone.0055147. Epub 2013 Jan 30.
2
Palindromic nucleotide analysis in human T cell receptor rearrangements.回文核苷酸分析在人类 T 细胞受体重排中。
PLoS One. 2012;7(12):e52250. doi: 10.1371/journal.pone.0052250. Epub 2012 Dec 21.
3
NOTCH1 nuclear interactome reveals key regulators of its transcriptional activity and oncogenic function.NOTCH1 核相互作用组揭示了其转录活性和致癌功能的关键调节因子。
Mol Cell. 2012 Nov 9;48(3):445-58. doi: 10.1016/j.molcel.2012.08.022. Epub 2012 Sep 27.
4
VDJ recombinase-mediated TCR β locus gene usage and coding joint processing in peripheral T cells during perinatal and pediatric development.在围生期和儿童期发育过程中,外周 T 细胞中的 VDJ 重组酶介导的 TCR β 基因座基因使用和编码连接处理。
J Immunol. 2012 Sep 1;189(5):2356-64. doi: 10.4049/jimmunol.1200382. Epub 2012 Aug 1.
5
Role of non-homologous end joining in V(D)J recombination.非同源末端连接在 V(D)J 重组中的作用。
Immunol Res. 2012 Dec;54(1-3):233-46. doi: 10.1007/s12026-012-8329-z.
6
Role of the transcription factor Bcl11b in development and lymphomagenesis.转录因子 Bcl11b 在发育和淋巴瘤发生中的作用。
Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(3):72-87. doi: 10.2183/pjab.88.72.
7
Illegitimate V(D)J recombination involving nonantigen receptor loci in lymphoid malignancy.淋巴恶性肿瘤中非抗原受体基因座的非法 V(D)J 重组。
Genes Chromosomes Cancer. 2012 Jun;51(6):525-35. doi: 10.1002/gcc.21942. Epub 2012 Feb 15.
8
The response to and repair of RAG-mediated DNA double-strand breaks.RAG 介导的 DNA 双链断裂的响应和修复。
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9
Chromatin topology and the regulation of antigen receptor assembly.染色质拓扑结构与抗原受体装配的调控。
Annu Rev Immunol. 2012;30:337-56. doi: 10.1146/annurev-immunol-020711-075003. Epub 2012 Jan 3.
10
V(D)J recombination: mechanisms of initiation.V(D)J 重组:起始机制。
Annu Rev Genet. 2011;45:167-202. doi: 10.1146/annurev-genet-110410-132552. Epub 2011 Aug 19.

Notch1 和 Bcl11b 中的非法 V(D)J 重组介导缺失不足以导致广泛的克隆扩增,并且在频率或连接加工方面不存在明显的年龄或性别偏向。

Illegitimate V(D)J recombination-mediated deletions in Notch1 and Bcl11b are not sufficient for extensive clonal expansion and show minimal age or sex bias in frequency or junctional processing.

机构信息

Department of Biological Sciences, Southeastern Louisiana University, Hammond, LA 70402, United States.

出版信息

Mutat Res. 2014 Mar;761:34-48. doi: 10.1016/j.mrfmmm.2014.01.007. Epub 2014 Feb 14.

DOI:10.1016/j.mrfmmm.2014.01.007
PMID:24530429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4075194/
Abstract

Illegitimate V(D)J recombination at oncogenes and tumor suppressor genes is implicated in formation of several T cell malignancies. Notch1 and Bcl11b, genes involved in developing T cell specification, selection, proliferation, and survival, were previously shown to contain hotspots for deletional illegitimate V(D)J recombination associated with radiation-induced thymic lymphoma. Interestingly, these deletions were also observed in wild-type animals. In this study, we conducted frequency, clonality, and junctional processing analyses of Notch1 and Bcl11b deletions during mouse development and compared results to published analyses of authentic V(D)J rearrangements at the T cell receptor beta (TCRβ) locus and illegitimate V(D)J deletions observed at the human, nonimmune HPRT1 locus not involved in T cell malignancies. We detect deletions in Notch1 and Bcl11b in thymic and splenic T cell populations, consistent with cells bearing deletions in the circulating lymphocyte pool. Deletions in thymus can occur in utero, increase in frequency between fetal and postnatal stages, are detected at all ages examined between fetal and 7 months, exhibit only limited clonality (contrasting with previous results in radiation-sensitive mouse strains), and consistent with previous reports are more frequent in Bcl11b, partially explained by relatively high Recombination Signal Information Content (RIC) scores. Deletion junctions in Bcl11b exhibit greater germline nucleotide loss, while in Notch1 palindromic (P) nucleotides are more abundant, although average P nucleotide length is similar for both genes and consistent with results at the TCRβ locus. Non-templated (N) nucleotide insertions appear to increase between fetal and postnatal stages for Notch1, consistent with normal terminal deoxynucleotidyl transferase (TdT) activity; however, neonatal Bcl11b junctions contain elevated levels of N insertions. Finally, contrasting with results at the HPRT1 locus, we find no obvious age or gender bias in junctional processing, and inverted repeats at recessed coding ends (Pr nucleotides) correspond mostly to single-base additions consistent with normal TdT activity.

摘要

致癌基因和肿瘤抑制基因中的非法 V(D)J 重组与几种 T 细胞恶性肿瘤的形成有关。Notch1 和 Bcl11b 是参与 T 细胞特异性、选择、增殖和存活发育的基因,先前已显示其包含与辐射诱导的胸腺淋巴瘤相关的缺失性非法 V(D)J 重组热点。有趣的是,这些缺失也在野生型动物中观察到。在这项研究中,我们在小鼠发育过程中对 Notch1 和 Bcl11b 的缺失进行了频率、克隆性和连接处理分析,并将结果与 TCRβ 基因座中真实的 V(D)J 重排和非免疫 HPRT1 基因座中观察到的与 T 细胞恶性肿瘤无关的非法 V(D)J 缺失的已发表分析进行了比较。我们在胸腺和脾脏 T 细胞群中检测到 Notch1 和 Bcl11b 的缺失,这与循环淋巴细胞池中带有缺失的细胞一致。胸腺中的缺失可在子宫内发生,在胎儿和出生后阶段的频率增加,在胎儿至 7 个月之间的所有年龄均有检测到,仅表现出有限的克隆性(与先前在辐射敏感的小鼠品系中的结果相反),并且与先前的报道一致,在 Bcl11b 中更为频繁,部分原因是相对较高的重组信号信息含量 (RIC) 评分。Bcl11b 中的缺失连接表现出更大的种系核苷酸丢失,而在 Notch1 中,回文(P)核苷酸更为丰富,尽管两个基因的平均 P 核苷酸长度相似,与 TCRβ 基因座的结果一致。非模板(N)核苷酸插入似乎在胎儿和出生后阶段增加 Notch1,这与正常末端脱氧核苷酸转移酶(TdT)活性一致;然而,新生 Bcl11b 连接含有高水平的 N 插入。最后,与 HPRT1 基因座的结果相反,我们没有发现连接处理中明显的年龄或性别偏见,并且凹陷编码末端(Pr 核苷酸)的反向重复主要对应于单个碱基添加,这与正常的 TdT 活性一致。