Pataer A, Kamoto T, Lu L M, Yamada Y, Hiai H
Department of Pathology and Biology of Disease, Graduate School of Medicine, Japan.
Cancer Res. 1996 Aug 15;56(16):3716-20.
To explore possible host genes suppressing spontaneous B-lymphomagenesis in the mouse, expression of ecotropic murine leukemia virus (E-MuLV) and lymphoma development were observed in crosses between the pre-B lymphoma-prone SL/Kh and low-lymphoma strains of mice. E-MuLV expression was intensely inhibited in F1 hybrids with the strains either with the Fv-1b allele (BALB/C, C57BL/10, and A/J) or with the Fv-1nr allele (NZB). In these F1 mice, no lymphoma developed by 18 months of age. On the other hand, F1 hybrids with the strains with the Fv-1n allele [C3H/He, CBA/N, SJL, DBA/2, and MSM/Ms (hereafter referred to as MSM)], high or intermediate levels of E-MuLV expression were observed. Lymphoma incidence in these F1 hybrids, however, was low. This observation suggests the presence of non-Fv-1 dominant resistance genes in these strains. In an attempt to characterize such host genes, we analyzed crosses between SL/Kh mice and a wild mouse-derived inbred strain, MSM/Ms. The latter was susceptible to N-tropic virus expression, but (SL/Kh x MSM)F1 hybrids, did not develop and lymphomas. Of 60 SL/Kh x (SL/Kh x MSM)F1 hybrids, 14 B-lineage lymphomas, including 13 pre-B and 1 follicular center cell lymphoma, developed by 18 months of age. This was compatible with the hypothesis of two independently segregating dominant genes of MSM suppressing lymphomagenesis. By scanning all chromosomes for linkage of lymphoma susceptibility with polymorphic microsatellite loci, one significant linkage disequilibrium was found in the proximal segment of chromosome 17, containing D17MIT44 (map position 15.0) to D17MIT150 (position 33.3), and another linkage disequilibrium, in the midproximal segment of chromosome 18, containing D18MIT90 (map position 28.0) and D18MIT140 (37.0). All 13 pre-B lymphoma-bearing backcross mice were homozygous for SL/Kh-derived alleles at these loci. We named the gene on chromosome 17 Msmr1 (for MSM resistance 1) and that on chromosome 18 Msmr 2 (for MSM resistance 2).
为了探索可能抑制小鼠自发性B淋巴细胞瘤发生的宿主基因,在易患前B淋巴瘤的SL/Kh小鼠与低淋巴瘤发生率的小鼠品系杂交过程中,观察了嗜亲性鼠白血病病毒(E-MuLV)的表达和淋巴瘤的发展情况。在与具有Fv-1b等位基因的品系(BALB/C、C57BL/10和A/J)或具有Fv-1nr等位基因的品系(NZB)杂交产生的F1代杂种小鼠中,E-MuLV的表达受到强烈抑制。在这些F1代小鼠中,到18月龄时没有发生淋巴瘤。另一方面,在与具有Fv-1n等位基因的品系[C3H/He、CBA/N、SJL、DBA/2和MSM/Ms(以下简称MSM)]杂交产生的F1代杂种小鼠中,观察到E-MuLV表达水平较高或中等。然而,这些F1代杂种小鼠的淋巴瘤发生率较低。这一观察结果表明,在这些品系中存在非Fv-1显性抗性基因。为了鉴定此类宿主基因,我们分析了SL/Kh小鼠与野生小鼠衍生的近交系MSM/Ms之间的杂交情况。后者易感染N嗜性病毒,但(SL/Kh×MSM)F1代杂种小鼠未发生淋巴瘤。在60只SL/Kh×(SL/Kh×MSM)F1代杂种小鼠中,到18月龄时,有14只发生了B系淋巴瘤,其中包括13只前B淋巴瘤和1只滤泡中心细胞淋巴瘤。这与MSM的两个独立分离的显性基因抑制淋巴瘤发生的假说相符。通过扫描所有染色体上淋巴瘤易感性与多态性微卫星位点的连锁关系,在17号染色体近端区段发现了一个显著的连锁不平衡,该区段包含D17MIT44(图谱位置15.0)至D17MIT150(位置33.3),在18号染色体近中近端区段发现了另一个连锁不平衡,该区段包含D18MIT90(图谱位置28.0)和D18MIT140(37.0)。所有13只携带前B淋巴瘤的回交小鼠在这些位点上均为SL/Kh衍生等位基因的纯合子。我们将17号染色体上的基因命名为Msmr1(代表MSM抗性1),将18号染色体上的基因命名为Msmr2(代表MSM抗性2)。