Fukuchi K, Sudo M, Lee Y S, Tanaka A, Nonoyama M
J Virol. 1984 Jul;51(1):102-9. doi: 10.1128/JVI.51.1.102-109.1984.
Purified virion DNA (120 X 10(6) molecular weight [MW]) of Marek's disease virus strain GA was cleaved with BamHI restriction endonuclease, and 27 out of the 29 fragments were cloned into bacterial plasmids. Restriction maps for BamHI, BglI, and SmaI endonucleases were constructed. The genomic structure of Marek's disease virus DNA was found to be similar to that of herpes simplex virus types 1 and 2. A long unique region (75 X 10(6) MW, located at 10 X 10(6) to 85 X 10(6) MW [10-85] from the left end of the genome), which was subdivided into segment 1 (22 X 10(6) MW, located at 10-32) and segment 2 (51 X 10(6) MW, located at 34-85) by direct repeats (32-34), was flanked by a long terminal region (10 X 10(6) MW, located at 0-10) and a long inverted region (10 X 10(6) MW, located at 85-95). A short unique region (8 X 10(6) MW, located at 103-111) was flanked by a short terminal region (8 X 10(6) MW, located at 111-119) and a short inverted region (8 X 10(6) MW, located at 95-103). The direct repeat fragments (0.9 X 10(6) could be isolated by cleavage with SmaI. The right terminal end was found to be heterogenous .
用BamHI限制性内切酶切割马立克氏病病毒GA株的纯化病毒粒子DNA(分子量[MW]为120×10⁶),29个片段中的27个被克隆到细菌质粒中。构建了BamHI、BglI和SmaI内切酶的限制性图谱。发现马立克氏病病毒DNA的基因组结构与1型和2型单纯疱疹病毒相似。一个长的单一区域(分子量为75×10⁶,位于基因组左端10×10⁶至85×10⁶MW[10 - 85]处),被直接重复序列(32 - 34)细分为片段1(分子量为22×10⁶,位于10 - 32处)和片段2(分子量为51×10⁶,位于34 - 85处),其两侧分别是一个长末端区域(分子量为10×10⁶,位于0 - 10处)和一个长反向区域(分子量为10×10⁶,位于85 - 95处)。一个短的单一区域(分子量为8×10⁶,位于103 - 111处)两侧分别是一个短末端区域(分子量为8×10⁶,位于111 - 119处)和一个短反向区域(分子量为8×10⁶,位于95 - 103处)。直接重复片段(0.9×10⁶)可用SmaI切割分离。发现右端末端是异质的。