Abstract
Phenotypic complementation of xeroderma pigmentosum group A (XP-A) cells by microcell-mediated transfer of a single rearranged neo-tagged human chromosome from a human-mouse somatic cell hybrid designated K3SUB1A9-3 was reported previously. Extended growth of this human-mouse hybrid in culture led to deletion of the small arm of the human chromosome, with concomitant loss of complementing ability when introduced into XP-A cells by microcell-mediated chromosome transfer. Cytogenetic analysis of both hybrids suggests that the complementing locus is on chromosome 9q22.2-q34.3, and Southern blot analysis confirms the presence of distal chromosome 9q sequences.
Original language | English (US) |
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Pages (from-to) | 395-400 |
Number of pages | 6 |
Journal | Somatic Cell and Molecular Genetics |
Volume | 16 |
Issue number | 4 |
DOIs | |
State | Published - Jul 1990 |
ASJC Scopus subject areas
- Genetics
- Cell Biology