Human Genetics

, Volume 124, Issue 5, pp 473–478

Gradual reduction of BUBR1 protein levels results in premature sister-chromatid separation then in aneuploidy

  • Elodie Bohers
  • Nasrin Sarafan-Vasseur
  • Aurélie Drouet
  • Marianne Paresy
  • Jean-Baptiste Latouche
  • Jean-Michel Flaman
  • Richard Sesboüé
  • Thierry Frebourg
Original Investigation

Abstract

Biallelic and heterozygous mutations of the BUB1B gene have been reported in mosaic variegated aneuploidy (MVA), a rare disorder characterized by constitutional mosaic aneuploidies associated to severe intrauterine growth retardation, microcephaly and, in most cases, to premature chromatid separation (PCS), highlighting the key role of human BUBR1 in chromosome segregation. To study the consequences of gradual reduction of the BUBR1 protein levels, inhibition of BUB1B expression in model cells was induced using short hairpin RNAs (shRNAs). We obtained stable shRNA-transduced HeLa cells displaying a gradient of residual BUBR1 protein (8.5, 10, 14, 58, and 77%), mimicking the situation of patients’ cells harboring one or two BUB1B mutations. Induction of PCS was detected in all transduced cells and its level was correlated to the decrease of BUBR1. Aneuploidy was clearly detected in cells with residual BUBR1 below 50%. Our data demonstrate that the function of the human BUBR1 protein in the spindle checkpoint is remarkably dosage-dependent and that the biological consequences of BUB1B expression reduction on premature chromatid separation and aneuploidy depend on the residual amount of BUBR1. This provides a biological explanation for the mode of inheritance of PCS, which is dominant, and of MVA, which can be recessive in some families and result from the combination of a null allele associated to a common hypomorphic allele in others.

Copyright information

© Springer-Verlag 2008

Authors and Affiliations

  • Elodie Bohers
    • 1
    • 2
  • Nasrin Sarafan-Vasseur
    • 1
    • 2
  • Aurélie Drouet
    • 1
    • 2
  • Marianne Paresy
    • 3
  • Jean-Baptiste Latouche
    • 1
    • 2
  • Jean-Michel Flaman
    • 1
    • 2
  • Richard Sesboüé
    • 1
    • 2
  • Thierry Frebourg
    • 1
    • 2
  1. 1.Faculty of MedicineINSERM U614RouenFrance
  2. 2.Department of GeneticsUniversity HospitalRouenFrance
  3. 3.Department of PathologyRouen University HospitalRouenFrance

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