4.2 Article

Centromere inactivation on a neo-Y fusion chromosome in threespine stickleback fish

Journal

CHROMOSOME RESEARCH
Volume 24, Issue 4, Pages 437-450

Publisher

SPRINGER
DOI: 10.1007/s10577-016-9535-7

Keywords

Dicentric chromosome fusion; Centromere inactivation; CENP-A; ChIP-seq; Gasterosteus aculeatus; Gasterosteus nipponicus

Funding

  1. National Science Foundation Graduate Research Fellowship [DGE-1256082]
  2. National Institutes of Health Chromosome Metabolism and Cancer Training Grant [T32 CA009657]
  3. National Institutes of Health grant [R01 GM116853]
  4. Fred Hutchinson Cancer Research Center

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Having one and only one centromere per chromosome is essential for proper chromosome segregation during both mitosis and meiosis. Chromosomes containing two centromeres are known as dicentric and often mis-segregate during cell division, resulting in aneuploidy or chromosome breakage. Dicentric chromosome can be stabilized by centromere inactivation, a process which reestablishes monocentric chromosomes. However, little is known about this process in naturally occurring dicentric chromosomes. Using a combination of fluorescence in situ hybridization (FISH) and immunofluorescence combined with FISH (IF-FISH) on metaphase chromosome spreads, we demonstrate that centromere inactivation has evolved on a neo-Y chromosome fusion in the Japan Sea threespine stickleback fish (Gasterosteus nipponicus). We found that the centromere derived from the ancestral Y chromosome has been inactivated. Our data further suggest that there have been genetic changes to this centromere in the two million years since the formation of the neo-Y chromosome, but it remains unclear whether these genetic changes are a cause or consequence of centromere inactivation.

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