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一名套细胞淋巴瘤患者中发现的新型bcl-1/JH断裂点扩展了主要易位簇。

A novel bcl-1/JH breakpoint from a patient affected by mantle cell lymphoma extends the major translocation cluster.

作者信息

Degan Massimo, Doliana Roberto, Gloghini Annunziata, Di Francia Raffaele, Aldinucci Donatella, Mazzocut-Zecchin Linda, Colombatti Alfonso, Attadia Vincenza, Carbone Antonino, Gattei Valter

机构信息

Clinical and Experimental Hematology Research Unit, Division of Experimental Oncology 2, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano I-33981, Italy.

出版信息

J Pathol. 2002 Jun;197(2):256-63. doi: 10.1002/path.1096.

Abstract

Mantle cell lymphoma (MCL) is a B-lymphocytic malignancy frequently associated with the presence of the t(11;14) chromosomal translocation. By using a polymerase chain reaction (PCR) strategy to detect breakpoints within the major translocation cluster (MTC), an unexpectedly large product (about 1.1 kb by using first-round bcl-1/JH primers) has been identified in one out of 16 patients harbouring the t(11;14) translocation. Sequence analysis of the atypical PCR product, re-amplified and cloned with second-round primers, revealed a 459 bp portion corresponding exactly to the 3'-end segment of the MTC, followed by a sequence of 433 bp that lacked homology with any previously known sequence. PCR experiments using DNA from healthy donors identified that fragment as an extension of MTC fused, through a N-region of seven nucleotides, to the JH4 region of IgH gene. A computer-based search of the novel MTC portion aimed at detecting potential recombination motifs revealed the presence of several 4-bp sequences (5'-CCAG-3' or its complement 5'-CTGG-3'), one of them within seven nucleotides from the putative breakpoint, known to play a role in non-homologous recombination events at the Ig loci. The recognition of this novel breakpoint may have important implications for the diagnosis and detection of minimal residual disease in t(11;14)-positive lymphomas.

摘要

套细胞淋巴瘤(MCL)是一种B淋巴细胞恶性肿瘤,常与t(11;14)染色体易位相关。通过使用聚合酶链反应(PCR)策略检测主要易位簇(MTC)内的断点,在16例携带t(11;14)易位的患者中,有1例鉴定出一个意外的大产物(使用第一轮bcl-1/JH引物时约为1.1 kb)。对非典型PCR产物进行测序分析,用第二轮引物重新扩增并克隆,结果显示一个459 bp的部分与MTC的3'-末端片段完全对应,随后是一个433 bp的序列,与任何先前已知序列均无同源性。使用健康供体的DNA进行的PCR实验确定该片段是MTC的延伸,通过一个7个核苷酸的N区域与IgH基因的JH4区域融合。对新的MTC部分进行基于计算机的搜索,旨在检测潜在的重组基序,结果发现存在几个4 bp序列(5'-CCAG-3'或其互补序列5'-CTGG-3'),其中一个位于距推定断点7个核苷酸内,已知其在Ig基因座的非同源重组事件中起作用。识别这个新的断点可能对t(11;14)阳性淋巴瘤的诊断和微小残留病的检测具有重要意义。

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