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用白血病病毒感染植入前小鼠胚胎和新生小鼠:病毒DNA和RNA的组织分布以及成年动物的白血病发生情况。

Infection of preimplantation mouse embryos and of newborn mice with leukemia virus: tissue distribution of viral DNA and RNA and leukemogenesis in the adult animal.

作者信息

Jaenisch R, Fan H, Croker B

出版信息

Proc Natl Acad Sci U S A. 1975 Oct;72(10):4008-12. doi: 10.1073/pnas.72.10.4008.

Abstract

Explanted mouse embryos derived from low leukemia incidence strains were infected with Moloney murine leukemia virus (M-MuLV) at the 4-8 cell stage of development. After cultivation in vitro to the blastocyst stage, the embryos were surgically transferred to the uteri of pseudo-pregnant surrogate mothers. Of 15 animals born, one developed a leukemia at 8 weeks of age. When autopsied, this leukemia was found to be of the lymphatic type, as is typical for the M-MuLV-induced disease. In addition, infectious M-MuLV virus was isolated from the serum. Molecular hybridization tests for the presence of M-MuLV-specific sequences were conducted on DNA and RNA extracted from eight different organs. The DNA-DNA reannealing experiments revealed the presence of two classes of M-MuLV-specific sequences in equal concentrations in all tissues tested. The less abundant class of M-MuLV-specific sequences was not detected in tissues from uninfected animals or in non-target tissues of leukemic animals infected at birth. The results are consistent with the working hypothesis that the virus was integrated in all cells of the animal, possibly including the germ line. Fifty to 100 times more M-MuLV-specific RNA was detected in tumor tissues than was found in non-target organs such as liver, brain, and testes. Since all organs contained the same amount of virus-specific DNA, these results indicate that the M-MuLV-specific DNA can be differentially expressed in different tissues.

摘要

将源自低白血病发病率品系的小鼠胚胎在发育的4-8细胞阶段用莫洛尼鼠白血病病毒(M-MuLV)感染。在体外培养至囊胚阶段后,通过手术将胚胎移植到假孕代孕母亲的子宫中。在出生的15只动物中,有一只在8周龄时患上了白血病。尸检时发现这种白血病是淋巴型的,这是M-MuLV诱导疾病的典型类型。此外,从血清中分离出了具有传染性的M-MuLV病毒。对从八个不同器官提取的DNA和RNA进行了M-MuLV特异性序列存在的分子杂交试验。DNA-DNA复性实验表明,在所有测试组织中均存在两类浓度相等的M-MuLV特异性序列。在未感染动物的组织或出生时感染的白血病动物的非靶组织中未检测到含量较少的M-MuLV特异性序列类别。这些结果与病毒整合到动物的所有细胞中,可能包括生殖系的工作假设一致。在肿瘤组织中检测到的M-MuLV特异性RNA比在肝脏、大脑和睾丸等非靶器官中多50至100倍。由于所有器官所含的病毒特异性DNA量相同,这些结果表明M-MuLV特异性DNA可以在不同组织中差异表达。

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