Jensen N A, Baron-Van Evercooren A, Mattei M G, Galiana E, Guron C, Pinçon-Raymond M, Baron H, Rouget P, Cuzin F, Rassoulzadegan M
Unité 273 de l'INSERM, Université de Nice, France.
Mol Biol Med. 1989 Dec;6(6):493-500.
Among a series of 44 transgenic families established after microinjection into fertilized eggs of a plasmid DNA where the structural gene for the large T antigen of polyoma virus is located downstream from the viral early promoter-enhancer region, one family with a hereditary neurological disorder was observed. At about three weeks of age, these animals developed a syndrome of constant tremor with recurrent seizures. Histological and ultra-structural examination revealed extensive dysmyelination in the white matter of the brain stem, cerebellum and spinal cord, as well as of peripheral nerves. This phenotype is reminiscent of that of the mouse "twitcher" (twi) mutant and of the human hereditary leukodystrophies. Expression of the viral sequences, assayed by Northern analysis and immunolabeling of T antigen, occurred predominantly in cells of the central nervous system. Integration of the transgene was mapped by in situ hybridization on metaphasic plaques in region B-C1 of chromosome 12 (where the twi locus was previously localized). Long-term cultures of cells with neural characteristics could be established readily from the brain of the transgenic mice.
在将多瘤病毒大T抗原的结构基因位于病毒早期启动子-增强子区域下游的质粒DNA显微注射到受精卵后建立的44个转基因家系中,观察到一个患有遗传性神经疾病的家系。在大约三周龄时,这些动物出现了持续震颤并伴有反复发作癫痫的综合征。组织学和超微结构检查显示,脑干、小脑和脊髓以及外周神经的白质中存在广泛的髓鞘形成异常。这种表型让人联想到小鼠“抽搐”(twi)突变体和人类遗传性脑白质营养不良的表型。通过Northern分析和T抗原免疫标记检测病毒序列的表达,主要发生在中枢神经系统的细胞中。通过原位杂交在12号染色体B-C1区域的中期斑块上对转基因的整合进行了定位(twi基因座先前定位于此)。可以很容易地从转基因小鼠的大脑中建立具有神经特征的细胞长期培养物。