Spontaneous occurrence of a Robertsonian fusion involving chromosome 19 bysingle whole-arm reciprocal translocation (WART) in wild-derived house mice

Citation
J. Catalan et al., Spontaneous occurrence of a Robertsonian fusion involving chromosome 19 bysingle whole-arm reciprocal translocation (WART) in wild-derived house mice, CHROMOS RES, 8(7), 2000, pp. 593-601
Citations number
46
Categorie Soggetti
Molecular Biology & Genetics
Journal title
CHROMOSOME RESEARCH
ISSN journal
09673849 → ACNP
Volume
8
Issue
7
Year of publication
2000
Pages
593 - 601
Database
ISI
SICI code
0967-3849(200010)8:7<593:SOOARF>2.0.ZU;2-N
Abstract
Chromosomal races of the house mouse (Mus musculus domesticus) bear Roberts onian (Rb) fusions, which consist of centric translocations between two non -homologous acrocentric chromosomes. The high level of diversity of these f usions in house mice is generated by de-novo formation of Rb fusions and su bsequent whole-arm reciprocal exchanges (WARTs). This paper describes the s pontaneous occurrence of a new Rb fusion, Rb(4.19), in progeny of wild-deri ved house mice segregating for Rb(4.12). The chromosomal mutation was trace d to a female which exhibited germline and somatic mosaicism indicating an early embryonic origin of the mutation. FISH analysis of centromerically-lo cated ribosomal genes suggested that no modification was observed on chromo somes 12 and 19 prior to or following the occurrence of Rb(4.19). Distribut ion of telomeric sequences showed that both Rb fusions lacked telomeres in their centromeric regions. It is argued that this spontaneous mutation most likely originated by single whole-arm reciprocal translocation (WART) betw een Rb(4.12) and an acrocentric chromosome 19, resulting in Rb(4.19) and a neo-acrocentric chromosome 12. Sequences required for centromeric function and proximal telomeres would have been transferred to the neo-chromosome 12 from chromosome 19 during the translocation. The existence of such WARTs w hich generate derived acrocentric chromosomes has several implications for chromosomal evolution in house mice.