Buchberg A M, Bedigian H G, Taylor B A, Brownell E, Ihle J N, Nagata S, Jenkins N A, Copeland N G
Mammalian Genetics Laboratory, BRI-Basic Research Program, NCI-Frederick Cancer Research Facility, Maryland 21701.
Oncogene Res. 1988;2(2):149-65.
A common site of ecotropic murine leukemia virus integration designated Evi-2 (ecotropic viral integration site-2) has been identified in BXH-2 myeloid tumors. As part of experiments to determine whether Evi-2 identified a new proto-oncogene locus involved in myeloid disease, we determined its chromosomal location. We mapped Evi-2 to mouse Chromosome 11 using standard recombinant inbred strain and genetic backcross analysis. We then determined the location of Evi-2 relative to other proto-oncogene and growth factor loci located on Chromosome 11 by interspecific backcross analysis. The loci included in this study were the proto-oncogene loci, Erbb, Erba, and Rel, as well as, Il-3 (interleukin-3), Csfgm (granulocyte-macrophage colony stimulating factor), and Trp53-1 (transforming protein p53). All loci except Erbb had been previously mapped to Chromosome 11 with the use of somatic cell hybrids and consequently their positions on Chromosome 11 were not known. One proto-oncogene, Erbb-2 (analogous to the neu proto-oncogene), and one growth factor locus, Csfg (granulocyte colony-stimulating factor), which had not been mapped in the mouse were also localized on Chromosome 11 using the interspecific backcross mice. Recombination between Evi-2 and all proto-oncogene and growth factor loci was demonstrated, suggesting that Evi-2 may ultimately identify a new proto-oncogene involved in myeloid disease. This study revealed a number of interesting conserved linkage groups common to mouse and man.
在BXH - 2髓系肿瘤中已鉴定出嗜亲性鼠白血病病毒整合的一个常见位点,命名为Evi - 2(嗜亲性病毒整合位点 - 2)。作为确定Evi - 2是否识别出参与髓系疾病的新原癌基因位点的实验的一部分,我们确定了它在染色体上的位置。我们使用标准重组近交系和遗传回交分析将Evi - 2定位到小鼠11号染色体上。然后,我们通过种间回交分析确定了Evi - 2相对于位于11号染色体上的其他原癌基因和生长因子位点的位置。本研究中包括的位点有原癌基因位点Erbb、Erba和Rel,以及白细胞介素 - 3(Il - 3)、粒细胞 - 巨噬细胞集落刺激因子(Csfgm)和转化蛋白p53(Trp53 - 1)。除Erbb外,所有位点此前已利用体细胞杂种定位到11号染色体上,因此它们在11号染色体上的位置并不明确。一个未在小鼠中定位的原癌基因Erbb - 2(类似于neu原癌基因)和一个生长因子位点粒细胞集落刺激因子(Csfg)也利用种间回交小鼠定位到了11号染色体上。已证实Evi - 2与所有原癌基因和生长因子位点之间发生了重组,这表明Evi - 2最终可能识别出一个参与髓系疾病的新原癌基因。这项研究揭示了一些小鼠和人类共有的有趣的保守连锁群。