Karyotype heterogeneity and unclassified chromosomal abnormalities

• Published in: Cytogenetic and genome research Vol. 139; no. 3; p. 144
• Main Authors: Heng, H H Q, Liu, G, Stevens, J B, Abdallah, B Y, Horne, S D, Ye, K J, Bremer, S W, Chowdhury, S K, Ye, C J
• Format: Journal Article
• Language: English
• Published: Switzerland 01-01-2013
• Subjects: Chromatin - genetics; Chromosome Aberrations; Chromosome Segregation; Genome, Human; Genomics - methods; Humans; Karyotyping; Stochastic Processes
• ISSN: 1424-859X
• DOI: 10.1159/000348682

In a departure from traditional gene-centric thinking with regard to cytogenetics and cytogenomics, the recently introduced genome theory calls upon a re-focusing of our attention on karyotype analyses of disease conditions. Karyotype heterogeneity has been demonstrated to be directly involved in the somatic cell evolution process which is the basis of many common and complex diseases such as cancer. To correctly use karyotype heterogeneity and apply it to monitor system instability, we need to include many seemingly unimportant non-specific chromosomal aberrations into our analysis. Traditionally, cytogenetic analysis has been focused on identifying recurrent types of abnormalities, particularly those that have been linked to specific diseases. In this perspective, drawing on the new framework of 4D-genomics, we will briefly review the importance of studying karyotype heterogeneity. We have also listed a number of overlooked chromosomal aberrations including defective mitotic figures, chromosome fragmentation as well as genome chaos. Finally, we call for the systematic discovery/characterization and classification of karyotype abnormalities in human diseases, as karyotype heterogeneity is the common factor that is essential for somatic cell evolution.