Ru M, Shustik C, Rassart E
Département des Sciences Biologiques, Université du Québec à Montréal, Canada.
J Virol. 1993 Aug;67(8):4722-31. doi: 10.1128/JVI.67.8.4722-4731.1993.
The Graffi murine leukemia virus (MuLV) is a retroviral mixture that induces predominantly myeloid leukemia in several inbred strains of mice. To analyze the viral component responsible for the myeloid leukemogenesis, we cloned several proviruses from a Graffi MuLV-infected cell line. Several infectious molecular clones were obtained that could be classified into two distinct groups of infectious MuLV. Both types of MuLV were nondefective, ecotropic, and NB tropic and induced granulocytic leukemia in BALB/c and NFS mice. Restriction enzyme analysis and molecular hybridization with several MuLV probes on one molecular clone from each group revealed that both groups are closely related to each other but are clearly distinct from all known retroviruses. One component of MuLV, however, induced leukemia with a shorter latency period and harbored a lengthier long terminal repeat. The long terminal repeat of the more leukemogenic component of MuLV had acquired a 60-bp perfect duplication in the U3 region. Analysis of the tumor DNAs with probes for the mouse T-cell receptor and immunoglobulin heavy chain genes revealed frequent rearrangements with one or both probes. This concomitant expression by leukemic cells of markers of different lineages, observed in human leukemias, has been termed "lineage infidelity" and confirms that the latter rearrangements are not restricted to hematopoietic precursors committed to lymphoid differentiation.
格拉菲小鼠白血病病毒(MuLV)是一种逆转录病毒混合物,在几种近交系小鼠中主要诱发髓系白血病。为了分析导致髓系白血病发生的病毒成分,我们从一个感染了格拉菲MuLV的细胞系中克隆了几个前病毒。获得了几个感染性分子克隆,它们可分为两类不同的感染性MuLV。这两种类型的MuLV都是无缺陷的、亲嗜性的和NB嗜性的,并在BALB/c和NFS小鼠中诱发粒细胞白血病。对每组中的一个分子克隆进行限制性内切酶分析以及与几种MuLV探针的分子杂交表明,这两组彼此密切相关,但明显不同于所有已知的逆转录病毒。然而,MuLV的一个成分诱发白血病的潜伏期较短,并且含有更长的长末端重复序列。MuLV中更具白血病诱导性的成分的长末端重复序列在U3区域获得了一个60个碱基对的完美重复。用小鼠T细胞受体和免疫球蛋白重链基因的探针分析肿瘤DNA,发现经常有一个或两个探针发生重排。在人类白血病中观察到的白血病细胞同时表达不同谱系的标志物,这种情况被称为“谱系不忠实”,并证实后者的重排并不局限于致力于淋巴样分化的造血前体。