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[染色体重排及其在大鼠胚胎细胞体外自发永生化和转化中的作用]

[Chromosomal rearrangements and their effects in spontaneous immortalization and transformation of rat embryo cells in vitro].

作者信息

Iartseva N M, Fedortseva R F, Artsybasheva I V

出版信息

Tsitologiia. 2007;49(4):311-21.

Abstract

G-banding analysis of LRec-1 and LRec-3, spontaneously immortalized cell lines from rat embryo fibroblast, revealed diploid karyotypes with specific clonal structural rearrangements of chromosomes 7 and 19 - del(7)(q11.2q22.1), t(7;19)(q11.1;q12) in malignant stage. Both clonal abnormalities of chromosomes 7 and 19 were also revealed in LRec-1k clone and LRec-1 sf cell line. Previous study of LRec-1 and LRec-3 cells showed the presence of karyotypes with pseudodiploid modal chromosome number, partial trisomy of chromosome 7 and same clonal structural rearrangements of chromosomes 7 and 19 in immortalized stage. In malignant stage, the trisomy 6 and new clonal structural rearrangements of chromosomes 1, 2, 11, 15, 18, 19 and of chromosomes 10, 20 were also found in LRec-1 sf and LRec-1 cells, accordingly. There were no new clonal structural chromosome rearrangements in LRec-1 k and LRec-3 cells. We compared locies of chromosomes involved in rearrangements with mapped genes on these chromosomes according to RATMAP. Supposedly these genes are involved in spontaneous immortalization of rat embryo fibroblast and malignant transformation of LRec-1 and LRec-3 cells and rearrangements of chromosomes 1, 2, 11, 15 and 18 facilitate expression of growth factors of LRec-1 sf cells.

摘要

对大鼠胚胎成纤维细胞自发永生化细胞系LRec - 1和LRec - 3进行G带分析,结果显示其核型为二倍体,在恶性阶段染色体7和19存在特定的克隆性结构重排——del(7)(q11.2q22.1)、t(7;19)(q11.1;q12)。在LRec - 1k克隆和LRec - 1 sf细胞系中也发现了染色体7和19的这两种克隆异常。先前对LRec - 1和LRec - 3细胞的研究表明,在永生化阶段存在假二倍体众数染色体数的核型、染色体7的部分三体以及染色体7和19相同的克隆性结构重排。在恶性阶段,LRec - 1 sf和LRec - 1细胞中还分别发现了染色体6三体以及染色体1、2、11、15、18、19和染色体10、20的新的克隆性结构重排。LRec - 1 k和LRec - 3细胞中未发现新的克隆性染色体结构重排。我们根据RATMAP将参与重排的染色体位点与这些染色体上的定位基因进行了比较。据推测,这些基因参与了大鼠胚胎成纤维细胞的自发永生化以及LRec - 1和LRec - 3细胞的恶性转化,染色体1、2、11、15和18的重排促进了LRec - 1 sf细胞生长因子的表达。

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