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莫洛尼白血病病毒的遗传传递:染色体整合位点的定位

Genetic transmission of Moloney leukemia virus: mapping of the chromosomal integration site.

作者信息

Doehmer J, Breindl M, Willecke K, Jaenisch R

出版信息

Haematol Blood Transfus. 1979;23:561-8. doi: 10.1007/978-3-642-67057-2_72.

Abstract

Mice genetically transmitting the exogenous Moloney leukemia virus (Balb/Mo) have been previously derived. These animals carried one copy of Moloney virus DNA (M-MuLV) in their germ line and transmitted the virus as a single Mendelian gene to the next generation. Homozygous BALB/Mo mice were used to genetically map the M-MuLV locus. Embryo fibroblasts were fused to established Chinese hamster cells and somatic cell hybrids were selected. Segregation of mouse chromosomal markers in the hybrids was correlated to the loss of M-MuLV-specific sequences as detected by molecular hybridization. Of 15 isozymes located on different mouse chromosomes only triosephosphate isomerase segregated syntenic with the M-MuLV gene, suggesting that the virus was integrated on chromosome No. 6. This was confirmed by sexual genetic experiments analyzing segregation of Moloney viremia and two markers on chromosome 6 and 15, respectively. The results show that M-MuLV expression is linked to wa-1 on chromosome 6 at a distance of about 30 map units. These data define a new genetic locus, Mov-1, representing the structural gene of M-MuLV in BALB/Mo mice.

摘要

先前已培育出能遗传外源性莫洛尼白血病病毒(Balb/Mo)的小鼠。这些动物的生殖系中携带一份莫洛尼病毒DNA(M-MuLV),并将该病毒作为一个单孟德尔基因传递给下一代。纯合BALB/Mo小鼠被用于对M-MuLV基因座进行遗传定位。将胚胎成纤维细胞与已建立的中国仓鼠细胞融合,并筛选出体细胞杂种。通过分子杂交检测,杂种中小鼠染色体标记的分离与M-MuLV特异性序列的丢失相关。在位于不同小鼠染色体上的15种同工酶中,只有磷酸丙糖异构酶与M-MuLV基因同线分离,这表明该病毒整合在6号染色体上。通过分别分析莫洛尼病毒血症以及6号和15号染色体上两个标记的分离情况的性遗传实验,证实了这一点。结果表明,M-MuLV的表达与6号染色体上的wa-1基因连锁,并相距约30个图距单位。这些数据定义了一个新的遗传基因座Mov-1,它代表BALB/Mo小鼠中M-MuLV的结构基因。

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