Transfer of yeast artificial chromosomes into mammalian cells and comparative study of their integrity
Author
dc.contributor.author
Gobin, Samuel J.P.
Author
dc.contributor.author
Alcaïde-Loridan, Catherine
Author
dc.contributor.author
Bono Merino, María Rosa
Author
dc.contributor.author
Ottone, Catherine
Author
dc.contributor.author
Chumakov, Ilya
Author
dc.contributor.author
Rothstein, Rodney
Author
dc.contributor.author
Fellous, Marc
Admission date
dc.date.accessioned
2018-12-20T14:34:27Z
Available date
dc.date.available
2018-12-20T14:34:27Z
Publication date
dc.date.issued
1995
Cita de ítem
dc.identifier.citation
Gene, Volumen 163, Issue 1, 2018, Pages 27-33
Identifier
dc.identifier.issn
03781119
Identifier
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10.1016/0378-1119(95)00399-Q
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/156553
Abstract
dc.description.abstract
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