Molecular definition of breakpoints associated with human Xq isochromosomes : Implications for mechanisms of formation

• Published in: American journal of human genetics Vol. 58; no. 1; pp. 154 - 160
• Main Authors: WOLFF, D. J, MILLER, A. P, VAN DYKE, D. L, SCHWARTZ, S, WILLARD, H. F
• Format: Journal Article
• Language: English
• Published: Chicago, IL University of Chicago Press 1996
• Subjects: Biological and medical sciences; Cell Line; Cells, Cultured; Centromere; Chromosome aberrations; Chromosome Mapping; Chromosomes, Artificial, Yeast; Female; Genetic Markers; Humans; In Situ Hybridization; Isochromosomes; Karyotyping; Medical genetics; Medical sciences; Multigene Family; Oligonucleotide Probes; Turner Syndrome - genetics; X Chromosome; Chromosomal aberration; Human; Abnormal chromosome; Chromosome break; Abnormal X chromosome; Isochromosome
• ISSN: 0002-9297; 1537-6605

To test the centromere misdivision model of isochromosome formation, we have defined the breakpoints of cytogenetically monocentric and dicentric Xq isochromosomes (i(Xq)) from Turner syndrome probands, using FISH with cosmids and YACs derived from a contig spanning proximal Xp. Seven different pericentromeric breakpoints were identified, with 10 of 11 of the i(Xq)s containing varying amounts of material from Xp. Only one of the eight cytogenetically monocentric i(Xq)s demonstrated a single alpha-satellite (DXZ1) signal, consistent with classical models involving centromere misdivision. The remaining seven were inconsistent with such a model and had breakpoints that spanned proximal Xp11.21: one was between DXZ1 and the most proximal marker, ZXDA; one occurred between the duplicated genes, ZXDA and ZXDB; two were approximately 2 Mb from DXZ1; two were adjacent to ALAS2 located 3.5 Mb from DXZ1; and the largest had a breakpoint just distal to DXS1013E, indicating the inclusion of 8 Mb of Xp DNA between centromeres. The three cytologically dicentric i(Xq)s had breakpoints distal to DXS423E in Xp11.22 and therefore contained > or = 12 Mb of DNA between centromeres. These data demonstrate that the majority of breakpoints resulting in i(Xq) formation are in band Xp11.2 and not in the centromere itself. Therefore, we hypothesize that the predominant mechanism of i(Xq) formation involves sequences in the proximal short arm that are prone to breakage and reunion events between sister chromatids or homologous X chromosomes.