Mak T W, Axelrad A A, Bernstein A
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5809-12. doi: 10.1073/pnas.76.11.5809.
We have recently demonstrated that normal hemopoietic cells express RNA sequences that are homologous to sequences specific for the Friend erythroleukemia virus genome [Bernstein, A., Gamble, C., Penrose, D. & Mak, T. W. (1979) Proc. Natl. Acad. Sci. USA 76, 4455-4459]. In this communication, we report that the Fv-2 locus, the major genetic determinant controlling host susceptibility to erythroleukemia induction by Friend leukemia virus, also controls the expression of endogenous sequences related to the replication-defective component of Friend leukemia virus, Friend spleen focus-forming virus (SFFV), in normal uninfected mice. Two independent congeneic pairs of mice [C57BL/6 (B6) and B6.S; B6 and B6.C(H-7(b))], differing only in a small region of the mouse genome including the Fv-2 locus, were used for this purpose. In both cases, molecular hybridization analysis indicated that the presence of SFFV-related RNA sequences in normal mice was associated with the Fv-2(s) allele: bone marrow or spleen cellular RNA from Fv-2(rr) B6 mice contained no detectable SFFV-related sequences, whereas their congeneic Fv-2(ss) pairs contained relatively high levels of these RNA sequences. The absence of these RNA sequences in Fv-2(rr) mice was not due to deletion of these sequences from the DNA of Fv-2(rr) mice. Repopulation of lethally irradiated Fv-2(rr) mice with syngeneic Fv-2(rr) bone marrow cells did not lead to any increase in the levels of these SFFV-related RNA sequences, suggesting that the expression of these sequences is still reduced or inhibited in actively cycling Fv-2(rr) hemopoietic cells. Infection with Friend leukemia virus resulted in the appearance of high levels of RNA homologous to SFFV-specific sequences in the leukemic spleens of B6.S (Fv-2(ss)) mice, whereas these cellular RNA sequences could not be detected in the spleens of Friend virus-infected B6 (Fv-2(rr)) mice. The demonstration that the same gene locus controls both the expression of exogenous SFFV-specific sequences and erythroleukemia induction by Friend leukemia virus suggests that these sequences may be necessary for erythroleukemic transformation. In addition, the finding that the Fv-2 gene locus controls the expression of endogenous SFFV-related sequences suggests that these sequences may also be involved in normal hemopoiesis.
我们最近已证明,正常造血细胞表达的RNA序列与弗瑞德氏红细胞白血病病毒基因组的特异性序列具有同源性[伯恩斯坦,A.,甘布尔,C.,彭罗斯,D. & 马克,T.W.(1979年)《美国国家科学院院刊》76,4455 - 4459]。在本通讯中,我们报告,Fv - 2基因座,即控制宿主对弗瑞德氏白血病病毒诱导红细胞白血病易感性的主要遗传决定因素,在正常未感染的小鼠中也控制着与弗瑞德氏白血病病毒复制缺陷成分弗瑞德氏脾集落形成病毒(SFFV)相关的内源性序列的表达。为此使用了两对独立的同类系小鼠[C57BL/6(B6)和B6.S;B6和B6.C(H - 7(b))],它们仅在包括Fv - 2基因座在内的小鼠基因组的一个小区域存在差异。在这两种情况下,分子杂交分析表明,正常小鼠中SFFV相关RNA序列的存在与Fv - 2(s)等位基因相关:Fv - 2(rr) B6小鼠的骨髓或脾细胞RNA中未检测到可检测的SFFV相关序列,而它们的同类系Fv - 2(ss)对则含有相对高水平的这些RNA序列。Fv - 2(rr)小鼠中这些RNA序列的缺失并非由于这些序列从Fv - 2(rr)小鼠的DNA中缺失。用同基因的Fv - 2(rr)骨髓细胞对致死性照射的Fv - 2(rr)小鼠进行再填充,并未导致这些SFFV相关RNA序列水平的任何增加,这表明在活跃循环的Fv - 2(rr)造血细胞中这些序列的表达仍然降低或受到抑制。用弗瑞德氏白血病病毒感染导致B6.S(Fv - 2(ss))小鼠白血病脾脏中出现与SFFV特异性序列同源的高水平RNA,而在弗瑞德氏病毒感染的B6(Fv - 2(rr))小鼠脾脏中无法检测到这些细胞RNA序列。同一基因座既控制外源性SFFV特异性序列的表达又控制弗瑞德氏白血病病毒诱导红细胞白血病的这一证明表明,这些序列可能是红细胞白血病转化所必需的。此外,Fv - 2基因座控制内源性SFFV相关序列表达的这一发现表明,这些序列也可能参与正常造血过程。