Yano Y
Section of Bacterial Infection, Hokkaido University, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1992 Nov;67(6):761-71.
MuLV-integration sites were analyzed on seventeen thymic leukemia cell lines which have been established from spontaneous thymic leukemias in AKR mice and bone marrow chimeras. Three proviral integration sites were identified; near c-myc, N-myc and pim-1. Among them the integrations near the N-myc were analyzed. Two cell lines from AKR and a cell line from [(BALB/c x B6) F1-->AKR] bone marrow chimera contained the proviral integration near N-myc. In all three cell lines the integration of the provirus was found 18 to 20 bp downstream of the translational termination codon. The partial sequence analysis of the integrated LTR cell line established from AKR thymic lymphomas was the same as AKV. In contrast, the LTR integrated in a cell line from a bone marrow chimera was different from that of MuLV so far reported.
对从AKR小鼠自发胸腺白血病和骨髓嵌合体中建立的17种胸腺白血病细胞系的莫洛尼鼠白血病病毒(MuLV)整合位点进行了分析。确定了三个前病毒整合位点,分别靠近c-myc、N-myc和pim-1。其中对靠近N-myc的整合进行了分析。来自AKR的两个细胞系和来自[(BALB/c×B6)F1→AKR]骨髓嵌合体的一个细胞系含有靠近N-myc的前病毒整合。在所有三个细胞系中,前病毒的整合位于翻译终止密码子下游18至20个碱基对处。从AKR胸腺淋巴瘤建立的整合LTR细胞系的部分序列分析与AKV相同。相比之下,整合在骨髓嵌合体细胞系中的LTR与迄今报道的MuLV不同。