Optimising human chromosome separation for the production of chromosome-specific DNA libraries by flow sorting
โ Scribed by P. Harris; E. Boyd; M. A. Ferguson-Smith
- Publisher
- Springer
- Year
- 1985
- Tongue
- English
- Weight
- 651 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
โฆ Synopsis
A number of cell lines, some containing chromosomes with distinctive heteromorphisms, have been flow karyotyped using a single laser flow sorter in an attempt to select those suitable for sorting all human chromosomes individually. Using the non-base-specific D N A stain ethidium bromide, chromosomes 3,4, 5, and 6 form individual peaks in practically all normal subjects, while the right combination of heteromorphisrns enables chromosomes 1, 2, 8, 9, 13, 16, 17, 18, 19, 20, 21, 22, and Y to be sorted separately. Two male cell lines, one containing a duplication and one a deletion of the X, produce flow karyotypes suitable for sorting chromosomes 7 and 8. The use of numerical chromosome abnormalities to enrich the sex chromosomes and the autosomes 18 and 21 is also illustrated. The DNA stain Hoechst 33258 binds preferentially to AT base pairs. Flow karyotypes produced with this fluorochrome separate some chromosomes not well separated with ethidium bromide. Chromosomes 5, 6, 8, 13, 14, 15, 17, and 20, and Y can be sorted individually with Hoechst 33258 with the right combination of heteromorphisms. Using these techniques, all human chromosomes apart from 10, 11, and 12 have been found as individual flow karyotype peaks, suitable for sorting with a high degree of purity.
๐ SIMILAR VOLUMES
DiGeorge syndrome (DGS) is a human developmental defect of the structures derived from the third and fourth pharyngeal pouches. It apparently arises due to deletion of 22q11. We describe a strategy for the isolation of DNA probes for this region. A deleted chromosome 22, which includes 22q11, was fl
A method combining flow sorting and molecular cytogenetic techniques for the identification of unknown marker chrornosomes is described. In this study, the bladder tumor cell line 182 was used, which was known t o carry a marker chromosome of the size of chromosome 7 in every cell. From the cytogene