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The meaning of stability. 稳定的意义。
Pub Date : 2020-07-27 DOI: 10.2307/j.ctt1wvwdr9.84
R. Lewontin
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引用次数: 303
Mechanisms of DNA uptake by cells. 细胞摄取DNA的机制。
Pub Date : 1977-05-12
S A Lacks
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引用次数: 0
The structure of late adenovirus type 2 messenger RNAs. 晚期腺病毒2型信使rna的结构。
Pub Date : 1977-05-12
R E Gelinas, L T Chow, R J Roberts, T R Broker, D F Klessig
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引用次数: 0
Teratocarcinoma cells as vehicles for mutant and foreign genes. 畸胎癌细胞作为突变基因和外源基因的载体。
Pub Date : 1977-05-12
B Mintz

Mouse malignant teratocarcinoma cells, upon injection into early embryos at the blastocyst stage, become integrated into the developing embryo and stably normalized. In the mosaic mice that are formed, tumor-derived cells can give rise to the full range of normal, functional somatic tissues, and also to germ cells from which progeny are obtained. Totipotent mouse teratocarcinoma cells thus provide a new and essentially parasexual means of generating entire animals. The advantages of in vitro and in vivo technologies can now therefore be combined to synthesize mice with experimentally useful mutations. After mutagenization of the teratocarcinoma cells in culture, and selection or screening for the desired mutant phenotype, cells of mutant clones are microinjected into genetically marked blastocysts for further differentiation and full gene expression within the framework of the organism. An example is the isolation, by 6-thioguanine resistance, of cells deficient in hypoxanthine-guanine phosphoribosyl transferase -- the same deficiency that characterizes human patients with the X-linked Lesch-Nyhan disease. In work in progress, these cells have been cycled into genetically marked blastocysts, where the tumor lineage has successfully given rise to fully differentiated tissue contributions in which the enzyme defect persists. Such experiments present numerous possibilities for introducing specific mutations into mice, toward the ends of studying gene mechanisms responsible for differentiation and of producing animal models of human genetic diseases. Teratocarcinoma cells may also serve as vehicles for introducing foreign genetic material into mice in order to facilitate analyses of gene control mechanisms in development and disease.

小鼠恶性畸胎癌细胞在囊胚期注入早期胚胎后,融入发育中的胚胎并稳定归一化。在形成的马赛克小鼠中,肿瘤来源的细胞可以产生各种正常的、功能性的体细胞组织,也可以产生生殖细胞,从中获得后代。因此,全能小鼠畸胎瘤细胞提供了一种新的、本质上是准性的产生整个动物的方法。因此,现在可以结合体外和体内技术的优点来合成具有实验上有用突变的小鼠。将培养的畸胎癌细胞诱变后,选择或筛选所需的突变表型,将突变克隆的细胞微注射到遗传标记的囊胚中,以进一步分化并在生物体框架内充分表达基因。一个例子是,通过对6-硫鸟嘌呤的耐药性,分离出缺乏次黄嘌呤-鸟嘌呤磷酸核糖基转移酶的细胞,这种缺陷与人类x连锁莱希-尼汉病患者的特征相同。在正在进行的工作中,这些细胞已被循环成具有遗传标记的囊胚,在囊胚中,肿瘤谱系已成功地产生了酶缺陷持续存在的完全分化的组织贡献。这类实验为将特定突变引入小鼠提供了许多可能性,目的是研究负责分化的基因机制,并建立人类遗传疾病的动物模型。畸胎癌细胞也可以作为将外来遗传物质引入小鼠体内的载体,以促进对发育和疾病中的基因控制机制的分析。
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引用次数: 0
Injection of tRNAs into somatic cells: search for in vivo systems to assay potential nonsense mutations in somatic cells. 向体细胞注射trna:寻找体内系统来测定体细胞中潜在的无义突变。
Pub Date : 1977-05-12
J E Celis
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引用次数: 0
Gene transfer experiments in Neurospora. 神经孢子虫基因转移实验。
Pub Date : 1977-05-12
N C Mishra
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引用次数: 0
The expression of cloned eukaryotic DNA in prokaryotes. 克隆真核DNA在原核生物中的表达。
Pub Date : 1977-05-12
J Carbon, B Ratzkin, L Clarke, D Richardson
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引用次数: 0
Viroids: autoinducing regulatory RNAs? 类病毒:自动诱导的调控rna ?
Pub Date : 1977-05-12
T O Diener
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引用次数: 0
Transformation of cultured cells to chloramphenicol resistance by purified mammalian mitochondrial DNA. 利用纯化的哺乳动物线粒体DNA将培养细胞转化为氯霉素抗性。
Pub Date : 1977-05-12
H G Coon, C Ho
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引用次数: 0
RNA-mediated manipulation of early chick embryonic gene functions in vitro. rna介导的鸡早期胚胎基因功能的体外调控。
Pub Date : 1977-05-12
M A Siddiqui, A K Deshpande, H H Arnold, S B Jakowlew, P A Crawford
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引用次数: 0
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