Small supernumerary marker chromosomes and the nuclear architecture of sperm – a study in a fertile and an infertile brother

Abstract

Small supernumerary marker chromosomes (sSMC) are found about four times more frequently in subfertile compared to the general population. The reason for this finding is still unclear. However, a connection of interphase architecture and genome function is suggested. And as we found in a previous study the presence of sSMC influences the nuclear architecture of peripheral blood cells and fibroblasts, we hypothesized that sSMC could have similar effects in sperm cells possibly leading to infertility. Here we applied for the first time 3-dimensional interphase fluorescence in situ hybridization (3D-FISH) to characterize the position of an extra-chromosome with respect to its sister- and selected other chromosomes (6, 15, 18, 19, 21, X, and Y) in sperm. Two sSMC carrier brothers with the identical sSMC derived from chromosome 15 were studied. One of the brothers was fertile and the other brother was infertile. Deviations from the normal positioning of chromosomes 21 and Y were seen in both brothers and for chromosomes 19 and X only in the infertile brother. Most striking were high rates of nullisomy and/or disomy for chromosomes 15, including sSMC (15), and 18 exclusively seen in the infertile brother. Overall, further evidence is provided that sSMC influence the nuclear architecture of a cell, including sperm. Further studies are necessary in sperm of fertile and infertile sSMC carriers to elaborate if the detected aneuploidy like that seen in the infertile brother is due to sSMC presence and disturbance of nuclear architecture.

• Fertile/infertile
• nuclear architecture
• small supernumerary marker chromosomes (sSMC)
• sperm

Acknowledgment

This study was supported in part by the Deutsche Forschungsgemeinschaft (DFG) (LI 820/46-1).

Declaration of interest

The authors report no declarations of interest.

Author contributions

Performed the 3D-FISH experiments and evaluation: TK, NK; Provided the samples and did their cytogenetic workup: NG; Final evaluation and drafting of the manuscript: TL; All authors contributed to the final version of the manuscript.