Keyeux G, Gilgenkrantz S, Lefranc G, Lefranc M P
Laboratoire d'Immunogénétique Moléculaire, UA CNRS 1191, Université des Sciences et Techniques du Languedoc, Montpellier, France.
Hum Genet. 1989 Jun;82(3):219-22. doi: 10.1007/BF00291158.
Molecular characterization of a ring chromosome 14 was carried out in a patient with the 46,XX,r(14) karyotype. The breakpoints shown by chromosome banding were within bands p11 and q32. Using molecular probes for the immunoglobulin heavy chain (IGH), D14S1 and PI loci located at 14q32, we showed that the IGH and D14S1 loci, located at 14q32.3 and 14q32.2 respectively, were deleted on the ring chromosome 14, but that the PI locus was not. Therefore, the chromosomal break lies between PI and D14S1. These results show that the order of these chromosome 14 markers is cen-PI-D14S1-IGH, in keeping with multipoint linkage data. Further molecular characterization of ring 14 chromosomes should lead to a detailed understanding of the molecular events and clinical consequences of the gene deletion associated with such chromosomal aberrations.
对一名核型为46,XX,r(14)的患者进行了14号环状染色体的分子特征分析。染色体显带显示的断点位于p11和q32带内。使用针对位于14q32的免疫球蛋白重链(IGH)、D14S1和PI基因座的分子探针,我们发现分别位于14q32.3和14q32.2的IGH和D14S1基因座在14号环状染色体上缺失,但PI基因座未缺失。因此,染色体断裂位于PI和D14S1之间。这些结果表明,这些14号染色体标记的顺序是cen-PI-D14S1-IGH,与多点连锁数据一致。对14号环状染色体的进一步分子特征分析应能深入了解与此类染色体畸变相关的基因缺失的分子事件和临床后果。