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正常核型小鼠及具有T/1:17/190Ca染色体易位的小鼠所诱发白血病的染色体模式

Chromosome pattern of leukemias induced in mice with normal karyotype and with T/1:17/190Ca chromosome translocation.

作者信息

Włodarska I

机构信息

Department of Tumour Biology, Institute of Oncology, Warsaw.

出版信息

Arch Immunol Ther Exp (Warsz). 1988;36(2):205-21.

PMID:3240056
Abstract

The chromosome pattern of leukemias induced by gamma-irradiation in the translocation T190/tf and in the genetically related tf/tf strain was analyzed. The degree of variation in chromosome numbers was similar in both experimental groups. Karyotypically, the tumors of both strains showed slight and less frequent higher degree of variability. The most consistent karyotypic change was trisomy of chromosome 15, whose frequency was similar in both strains. In one of the leukemias a marker chromosome derived by translocation involving chromosome 15 was identified. Comparison of the breakpoint in this translocation with literature data on other translocations of chromosome 15 found in leukemias enabled narrowing the region on chromosome 15 containing the postulated genes essential for murine leukemogenesis. The incidence of leukemias was lower in the T190/tf translocation strain than in the tf/tf strain with normal karyotype.

摘要

对易位T190/tf和遗传相关的tf/tf品系中由γ射线诱导的白血病的染色体模式进行了分析。两个实验组中染色体数目的变异程度相似。从核型上看,两个品系的肿瘤均表现出轻微且频率较低的较高程度的变异性。最一致的核型变化是15号染色体三体,其频率在两个品系中相似。在一例白血病中鉴定出一条由涉及15号染色体的易位产生的标记染色体。将该易位的断点与白血病中发现的其他15号染色体易位的文献数据进行比较,使得能够缩小15号染色体上包含假定的对小鼠白血病发生至关重要的基因的区域。易位T190/tf品系中的白血病发病率低于核型正常的tf/tf品系。

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