Svoboda J, Plachý J, Hejnar J, Karakoz I, Guntaka R V, Geryk J
Department of Cellular and Viral Genetics, Czechoslovak Academy of Sciences, Prague.
Immunogenetics. 1992;35(5):309-15. doi: 10.1007/BF00189893.
We report that the cloned DNA harboring the long terminal repeat (LTR), v-src, LTR proviral structure is tumorigenic in chickens of the Prague congenic lines. The growth rate of these tumors is by far the highest in the recombinant CC.R1 line, the B haplotype of which is composed of the B-F/L4 and B-G12 subregions originating from different naturally occurring haplotypes. Some of the tumors induced by the LTR, v-src, LTR DNA are repeatedly transplantable in syngeneic chickens, maintain unaltered provirus, and express v-src mRNA. Differences in the response to challenge with Rous sarcoma virus (RSV) and LTR, v-src, LTR DNA on a given experimental model are compared and possible involvement of an interaction between B-F/L and B-G region genes is considered. Regression of the LTR, v-src, LTR DNA-induced tumors did not prevent the formation and growth of tumors induced subsequently by RSV.
我们报告,含有长末端重复序列(LTR)、v-src、LTR前病毒结构的克隆DNA在布拉格同基因系鸡中具有致瘤性。这些肿瘤的生长速度在重组CC.R1系中是迄今为止最高的,其B单倍型由源自不同自然发生单倍型的B-F/L4和B-G12亚区域组成。一些由LTR、v-src、LTR DNA诱导的肿瘤可在同基因鸡中反复移植,维持未改变的前病毒,并表达v-src mRNA。比较了在给定实验模型中对劳氏肉瘤病毒(RSV)和LTR、v-src、LTR DNA攻击的反应差异,并考虑了B-F/L和B-G区域基因之间相互作用的可能参与情况。LTR、v-src、LTR DNA诱导的肿瘤消退并未阻止随后由RSV诱导的肿瘤的形成和生长。