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B细胞淋巴瘤中BCL-1基因座内的多个断点:细胞周期蛋白D1基因的重排。

Multiple breakpoints within the BCL-1 locus in B-cell lymphoma: rearrangements of the cyclin D1 gene.

作者信息

de Boer C J, Loyson S, Kluin P M, Kluin-Nelemans H C, Schuuring E, van Krieken J H

机构信息

Department of Pathology, University of Leiden, The Netherlands.

出版信息

Cancer Res. 1993 Sep 15;53(18):4148-52.

PMID:8364907
Abstract

Centrocytic lymphoma (CC) and intermediately differentiated lymphocytic lymphoma (IDL) are B-cell non-Hodgkin's lymphomas composed of lymphocytes presumably derived from follicle mantle cells. In these lymphomas, a specific chromosomal translocation, t(11;14)(q13;q32), has been described. Previous studies suggested an association between t(11;14) chromosomal translocations and BCL-1 rearrangements. To evaluate the association between BCL-1 rearrangements and CC/IDL, Southern blot analysis was performed on a panel of 20 cases of CC/IDL, 22 cases of morphologically similar non-Hodgkin's lymphomas, 11 cases of chronic B-cell leukemias, and 2 cases of myelomas. We used various probes covering a considerable proportion of the 120-kilobase BCL-1 locus, and rearrangements in 50% of CC/IDL (10 of 20) were detected. In CC, all 4 breakpoints were located at the major translocation cluster (MTC). In contrast, in IDL, rearrangements were detected in 3 different cluster regions: 2 cases in the MTC, 2 cases with a breakpoint 24 kilobases outside the MTC, and 2 additional cases with breakpoints found 3 kilobases 5' of the first exon of the PRAD1/CCND1 gene, which is located 120 kilobases outside the MTC. In addition, one leukemia showed a breakpoint 63 kilobases outside the MTC. In all cases, there was comigration of the rearranged 11q13 fragment and the immunoglobulin heavy chain-joining gene complex, indicating a t(11;14)(q13;q32) chromosomal rearrangement. Our results show that Southern blot analysis is helpful to identify CC/IDL, but multiple breakpoints are present over a large region, and therefore, many probes are necessary to cover all breakpoints.

摘要

中心细胞性淋巴瘤(CC)和中等分化淋巴细胞性淋巴瘤(IDL)是B细胞非霍奇金淋巴瘤,由可能来源于滤泡套细胞的淋巴细胞组成。在这些淋巴瘤中,已描述了一种特定的染色体易位,即t(11;14)(q13;q32)。先前的研究表明t(11;14)染色体易位与BCL-1重排之间存在关联。为了评估BCL-1重排与CC/IDL之间的关联,对20例CC/IDL、22例形态学相似的非霍奇金淋巴瘤、11例慢性B细胞白血病和2例骨髓瘤进行了Southern印迹分析。我们使用了覆盖120千碱基BCL-1基因座相当大部分的各种探针,在50%的CC/IDL(20例中的10例)中检测到重排。在CC中,所有4个断点都位于主要易位簇(MTC)。相比之下,在IDL中,在3个不同的簇区域检测到重排:2例在MTC,2例断点在MTC外24千碱基处,另外2例断点在PRAD1/CCND1基因第一个外显子5'端3千碱基处,该基因位于MTC外120千碱基处。此外,1例白血病显示断点在MTC外63千碱基处。在所有病例中,重排的11q13片段与免疫球蛋白重链连接基因复合体共迁移,表明存在t(11;14)(q13;q32)染色体重排。我们的结果表明,Southern印迹分析有助于识别CC/IDL,但在一个大区域内存在多个断点,因此,需要许多探针来覆盖所有断点。

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