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IgD类别转换:肿瘤性和正常B细胞中一个新重组位点的鉴定

IgD class switching: identification of a novel recombination site in neoplastic and normal B cells.

作者信息

Kluin P M, Kayano H, Zani V J, Kluin-Nelemans H C, Tucker P W, Satterwhite E, Dyer M J

机构信息

Academic Department of Hematology and Cytogenetics, Royal Marsden Hospital, Sutton, GB.

出版信息

Eur J Immunol. 1995 Dec;25(12):3504-8. doi: 10.1002/eji.1830251244.

DOI:10.1002/eji.1830251244
PMID:8566044
Abstract

IgD on normal B lymphocytes usually is co-expressed with IgM. A minority of normal plasma cells and rare B cell malignancies express exclusively IgD (IgM-IgD+). The low frequency has been explained by the lack of a recognizable switch region within the C mu-C delta intron. We analyzed four cases of IgM-IgD+ hairy cell leukemia (HCL) by Southern (DNA) blot analysis and identified two cases with a recombinatorial event within the C mu-C delta intron and deletion of C mu. DNA sequence analysis of junctional regions showed that S mu or the immediate upstream region was used as a donor site and that the C mu-C delta intronic sigma delta region was used as acceptor site. Using polymerase chain reaction, we subsequently analyzed whether similar S mu-sigma delta recombinations occur in normal tonsils containing IgM-IgD+ plasma cells. Multiple products with a size range of 200-800 base pairs were detected in all four individuals, suggesting clustering of acceptor sites within sigma delta. Sequence analysis of three cloned products showed S mu-sigma delta recombinations similar those observed in HCL. The sigma delta region contains a relatively high content of pentameric repeats with an extremely G-rich area and appears to function as a vestigial switch recombination site in normal and neoplastic IgM-IgD+ B cells.

摘要

正常B淋巴细胞上的IgD通常与IgM共表达。少数正常浆细胞和罕见的B细胞恶性肿瘤仅表达IgD(IgM-IgD+)。这种低频率现象被解释为Cμ-Cδ内含子中缺乏可识别的转换区。我们通过Southern(DNA)印迹分析对4例IgM-IgD+毛细胞白血病(HCL)进行了分析,发现2例在Cμ-Cδ内含子内发生重组事件且Cμ缺失。连接区的DNA序列分析表明,Sμ或紧邻的上游区域被用作供体位点,Cμ-Cδ内含子的σδ区域被用作受体位点。随后,我们使用聚合酶链反应分析了含有IgM-IgD+浆细胞的正常扁桃体中是否发生类似的Sμ-σδ重组。在所有4名个体中均检测到大小范围为200-800个碱基对的多种产物,提示σδ内受体位点成簇。对3个克隆产物的序列分析显示,Sμ-σδ重组与在HCL中观察到的类似。σδ区域含有相对较高含量的五聚体重复序列以及一个富含G的区域,在正常和肿瘤性IgM-IgD+B细胞中似乎起着残留转换重组位点的作用。

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