16Measurements of nuclear organization in asymmetric nuclei in 2D images have traditionally been manual. 17 This is exemplified by attempts to measure chromosome position in sperm samples, typically by dividing the 18 nucleus into zones, and manually scoring which zone a FISH signal lies in. This is time consuming, limiting 19 the number of nuclei that can be analyzed, and prone to subjectivity. We have developed a new approach for 20 automated mapping of FISH signals in asymmetric nuclei, integrated into an existing image analysis tool for 21 nuclear morphology. Automatic landmark detection defines equivalent structural regions in each nucleus, then 22 dynamic warping of the FISH images to a common shape allows us to generate a composite of the signal 23 within the entire cell population. Using this approach, we mapped the positions of the sex chromosomes and 24 two autosomes in three mouse lineages (Mus musculus domesticus, Mus musculus musculus and Mus spretus).
25We found that in all three, chromosomes 11 and 19 tend to interact with each other, but are shielded from 26 interactions with the sex chromosomes. This organization is conserved across 2 million years of mouse 27 evolution.
62Mus musculus domesticus and Mus spretus. Of these, M. spretus has a notably different nuclear shape [18] to 63 the others, being shorter and wider, allowing us to test whether chromosome position is conserved across 64 structurally equivalent regions.
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Materials and Methods
66Sample collection 67 68We collected sperm from wild-derived inbred mouse strains Mus musculus musculus (PWK/PhJ), M. m. 69 domesticus (LEWES/EiJ) and Mus spretus (STF). All animal procedures were in accordance with the University 70 of Montana Institute for Animal Care and Use Committee (protocol 002-13) and were subject to local ethical 71 review. Animals were bred at the University of Montana from mice purchased from Jackson Laboratories (Bar 72Harbor, ME) or were acquired from Francois Bonhomme (University of Montpellier). Animals were housed 73 singly or in small groups, sacrificed via CO2 followed by cervical dislocation, and tissues were collected post 74 mortem for analysis. Sperm were collected and fixed in 3:1 methanol-acetic acid as previously described [18].
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