Bedigian H G, Copeland N G, Jenkins N A, Salvatore K, Rodick S
J Virol. 1983 May;46(2):490-7. doi: 10.1128/JVI.46.2.490-497.1983.
All AKR/J mice carry at least three endogenous ecotropic viral loci which have been designated Emv-11 (Akv-1), Emv-13 (Akv-3), and Emv-14 (Akv-4) (Jenkins et al., J. Virol. 43:26-36, 1982.) Using two independent AKR/J-derived sets of recombinant inbred mouse strains, AKXL (AKR/J x C57L/J) and AKXD (AKR/J x DBA/2J), as well as the HP/EiTy strain (an Emv-13-carrying inbred strain partially related to AKR/J mice) (Taylor et al., J. Virol. 23:106-109, 1977), we have examined the association of these endogenous viral loci with virus expression. Strains which transmit Emv-11 or Emv-14 or both were found to produce virus spontaneously, whereas strains that transmit Emv-13 alone were negative for virus expression. Restriction endonuclease digestion and hybridization with an ecotropic virus-specific hybridization probe of DNAs from strains which transmit only Emv-13 yielded enzyme cleavage patterns identical to those observed with DNAs from strains transmitting Emv-11 or Emv-14 or both. These findings indicate the absence of any gross rearrangement of Emv-13 proviral sequences. Cell cultures derived from recombinant inbred strains that carry only Emv-13 failed to express detectable infectious virus, viral proteins, or cytoplasmic ecotropic virus-specific RNA even after treatment with 5-iodo-2-deoxyuridine or 5-azacytidine, an inhibitor of DNA methylation. Our results indicate that a mechanism(s) other than methylation of Emv-13 proviral DNA is responsible for inhibition of Emv-13 expression.
所有AKR/J小鼠至少携带三个内源性亲嗜性病毒基因座,分别命名为Emv - 11(Akv - 1)、Emv - 13(Akv - 3)和Emv - 14(Akv - 4)(詹金斯等人,《病毒学杂志》43:26 - 36,1982年)。利用两组独立的源自AKR/J的重组近交小鼠品系AKXL(AKR/J×C57L/J)和AKXD(AKR/J×DBA/2J),以及HP/EiTy品系(一种携带Emv - 13的近交品系,与AKR/J小鼠有部分亲缘关系)(泰勒等人,《病毒学杂志》23:106 - 109,1977年),我们研究了这些内源性病毒基因座与病毒表达的关联。发现传递Emv - 11或Emv - 14或两者的品系能自发产生病毒,而仅传递Emv - 13的品系病毒表达呈阴性。对仅传递Emv - 13的品系的DNA进行限制性内切酶消化,并与亲嗜性病毒特异性杂交探针杂交,得到的酶切图谱与传递Emv - 11或Emv - 14或两者的品系的DNA观察到的图谱相同。这些发现表明Emv - 13前病毒序列没有任何明显重排。即使在用5 - 碘 - 2 - 脱氧尿苷或DNA甲基化抑制剂5 - 氮杂胞苷处理后,源自仅携带Emv - 13的重组近交品系的细胞培养物仍未能表达可检测到的感染性病毒、病毒蛋白或细胞质亲嗜性病毒特异性RNA。我们的结果表明,除了Emv - 13前病毒DNA甲基化之外的一种机制负责抑制Emv - 13的表达。