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SV40介导的肿瘤选择和染色体转移以富集囊性纤维化区域。

SV40-mediated tumor selection and chromosome transfer to enrich for cystic fibrosis region.

作者信息

Porteous D J, Dorin J R, Wilkinson M M, Fletcher J M, Emslie E, van Heyningen V

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.

出版信息

Somat Cell Mol Genet. 1990 Jan;16(1):29-38. doi: 10.1007/BF01650477.

Abstract

The somatic cell hybrid C121, with chromosome 7 as its sole human component, arose when mouse macrophages SV40 genomes are integrated at 7q31-7q35. We show that hybrids with a reduced chromosome 7 component, but which retain markers linked to the cystic fibrosis locus, can be generated by direct in vivo tumor selection or following chromosome-mediated gene transfer and SV40-mediated cellular transformation. Our methods for chromosome fragmentation and fine-structure mapping can now be applied to the substantial number of SV40-transformed human cell lines, with independent chromosomal integration sites, already available. Our results also suggest that expression of human epidermal growth factor receptor augments the tumorigenic potential of the SV40-transformed C121 hybrid.

摘要

体细胞杂种C121以7号染色体作为其唯一的人类成分,它是在小鼠巨噬细胞的SV40基因组整合到7q31 - 7q35时产生的。我们发现,通过直接的体内肿瘤筛选或经染色体介导的基因转移以及SV40介导的细胞转化,可以产生7号染色体成分减少但仍保留与囊性纤维化基因座相关标记的杂种。我们的染色体片段化和精细结构作图方法现在可应用于大量已有的、具有独立染色体整合位点的SV40转化的人类细胞系。我们的结果还表明,人类表皮生长因子受体的表达增强了SV40转化的C121杂种的致瘤潜力。

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