Gobin S J, Alcaïde-Loridan C, Bono M R, Ottone C, Chumakov I, Rothstein R, Fellous M
Immunogénétique Humaine, INSERM U276, Institut Pasteur, Paris, France.
Gene. 1995 Sep 22;163(1):27-33. doi: 10.1016/0378-1119(95)00399-q.
Yeast artificial chromosomes (YACs) from the CEPH MegaYAC library (Paris, France) ranging in size from 350 to 1600 kb and mapping to the q22.1 and q22.2 regions of human chromosome 21 were transferred into mammalian cells by spheroplast fusion. The integrity of the YACs from two adjacent parts of the region was compared after retrofitting and stable transfer into mammalian cells. We found that large YACs could easily be manipulated to allow transfer of the YAC material into mammalian cells and that the size of the YAC did not appear to be limiting for fusion. However, we show that there was great variability in the integrity of the YACs from the two regions, which was not related to the size of the YACs. Four YACs in region I from sequence-tagged site (STS) G51E05 up to STS LL103 showed, in general, no loss of material and correct gene transfer into mammalian cells. In contrast, the three YACs in the more centromeric region II (from STS G51B09 up to G51E05) frequently showed a loss of human material during handling, retrofitting and transfer. As a YAC from another library covering region II was also found to be unstable, we propose that the integrity of the YACs is highly dependent on the incorporated human chromosomal DNA.
来自法国巴黎CEPH MegaYAC文库、大小在350至1600 kb之间且定位于人类21号染色体q22.1和q22.2区域的酵母人工染色体(YAC),通过原生质球融合被转入哺乳动物细胞。在改造并稳定转入哺乳动物细胞后,比较了该区域两个相邻部分的YAC的完整性。我们发现,大型YAC能够很容易地进行操作,以便将YAC物质转入哺乳动物细胞,而且YAC的大小似乎对融合没有限制。然而,我们发现这两个区域的YAC完整性存在很大差异,这与YAC的大小无关。从序列标签位点(STS)G51E05到STS LL103的区域I中的四个YAC,总体上没有物质损失,并且向哺乳动物细胞的基因转移正确。相比之下,着丝粒较多的区域II中的三个YAC(从STS G51B09到G51E05)在处理、改造和转移过程中经常出现人类物质损失。由于发现来自另一个覆盖区域II的文库的一个YAC也不稳定,我们提出YAC的完整性高度依赖于整合的人类染色体DNA。