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具有8号与22号染色体易位的北美伯基特(NAB-2)淋巴瘤细胞系中的癌基因表达与免疫球蛋白合成

Oncogene expression and immunoglobulin synthesis in a North American Burkitt (NAB-2) lymphoma cell line with a 8;22 chromosome translocation.

作者信息

Popescu N C, Dahlberg J E, Ablashi D V, Monastier M, Bona C A, DiPaolo J A, Hooper W C, Swan D C

机构信息

Laboratory of Biology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

Oncogene Res. 1990;5(4):295-303.

PMID:1697668
Abstract

A Burkitt's lymphoma (BL) cell line, (NAB-2) deriving from a North American patient, exhibited a 8;22 (q22;q11-12) translocation involving the c-myc gene and lambda immunoglobulin genes. In addition, NAB-2 cells have two other consistent translocations: a 1;5 (p22;q23) and a 3;7 (p25;q22), with breakpoints close to the location of N-ras, fms, and raf-1 protooncogenes, respectively. In situ hybridization with myc, N-ras, and raf-1 radiolabeled DNA probes to NAB-2 chromosomes showed that none of these genes was relocated as a result of translocation. However, by Northern blot analysis, the myc mRNA was represented by two transcripts, one approximately 2.4 kb and the other considerably larger (74 kb). The raf-1 gene transcript was also detected in NAB-2 cells; however, its size and level were similar to those seen in two other BL lines. On the other hand, the N-ras, fms, and fgr genes, which are frequently activated in BL, were not actively transcribed. NAB-2 cells also have a chromatid defect visible as an achromatic region on the short arm of chromosome 2 near the locus of the kappa immunoglobulin gene. This alteration, which is a viral modification site caused by the Epstein-Barr virus or viral products, had no influence on immunoglobulin synthesis, as NAB-2 cells concordant to the 8;22 translocation were positive for cytoplasmic and surface lambda light chains. Although NAB-2 cells exhibit several chromosomal abnormalities, only translocation, 8;22 was associated with gene alterations relevant to the neoplastic development of this malignancy.

摘要

一种源自北美患者的伯基特淋巴瘤(BL)细胞系(NAB - 2),呈现出涉及c - myc基因和λ免疫球蛋白基因的8;22(q22;q11 - 12)易位。此外,NAB - 2细胞还有另外两个一致的易位:一个是1;5(p22;q23),另一个是3;7(p25;q22),其断点分别靠近N - ras、fms和raf - 1原癌基因的位置。用myc、N - ras和raf - 1放射性标记的DNA探针与NAB - 2染色体进行原位杂交显示,这些基因均未因易位而重新定位。然而,通过Northern印迹分析,myc mRNA由两种转录本代表,一种约2.4 kb,另一种则大得多(74 kb)。在NAB - 2细胞中也检测到了raf - 1基因转录本;然而,其大小和水平与另外两个BL细胞系中的相似。另一方面,在BL中经常被激活的N - ras、fms和fgr基因并未被积极转录。NAB - 2细胞在靠近κ免疫球蛋白基因位点的2号染色体短臂上还有一个可见的染色单体缺陷,表现为一个无色区域。这种改变是由爱泼斯坦 - 巴尔病毒或病毒产物引起的病毒修饰位点,对免疫球蛋白合成没有影响,因为与8;22易位一致的NAB - 2细胞的细胞质和表面λ轻链呈阳性。尽管NAB - 2细胞表现出几种染色体异常,但只有8;22易位与这种恶性肿瘤的肿瘤发生相关的基因改变有关。

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