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伴有t(11;14)(q23;q32)易位的B细胞淋巴瘤染色体断点的分子克隆

Molecular cloning of the chromosomal breakpoint of a B-cell lymphoma with the t(11;14)(q23;q32) translocation.

作者信息

Akao Y, Seto M, Takahashi T, Kubonishi I, Miyoshi I, Nakazawa S, Tsujimoto Y, Croce C M, Ueda R

机构信息

Laboratories of Chemotherapy and Immunology, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

Cancer Res. 1991 Mar 1;51(5):1574-6.

PMID:1997200
Abstract

The breakpoint of t(11;14)(q23;q32) chromosome translocation in a B-cell lymphoma line, RC-K8, was cloned. Immunoglobulin heavy chain (IGH) constant gene, C gamma 2 at the 5' end, was involved in this translocation, and the DNA segment juxtaposed to the C gamma 2 was proved to be derived from chromosome 11 by somatic cell hybrid study. The normal counterpart of chromosome 11 was also isolated. With a DNA probe near the breakpoint of chromosome 11, Southern blot analysis of RC-K8 and 10 other cases with translocation involving the 11q23 region was conducted, but no rearrangement bands have been observed thus far except for RC-K8.

摘要

在一个B细胞淋巴瘤系RC-K8中,克隆出了t(11;14)(q23;q32)染色体易位的断点。免疫球蛋白重链(IGH)恒定基因,5'端的Cγ2,参与了此次易位,并且通过体细胞杂交研究证明,与Cγ2并列的DNA片段来源于11号染色体。11号染色体的正常对应物也被分离出来。用一个靠近11号染色体断点的DNA探针,对RC-K8和其他10例涉及11q23区域易位的病例进行了Southern印迹分析,但迄今为止,除了RC-K8外,未观察到重排条带。

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