Comparative Cytology of Female Meiosis I Among Species.

G3 (Bethesda)

Department of Biological Sciences, DePaul University, 2325 N. Clifton Ave., Chicago IL 60614

Published: May 2020

The physical connections established by recombination are normally sufficient to ensure proper chromosome segregation during female Meiosis I. However, nonexchange chromosomes (such as the Muller element or "dot" chromosome in can still segregate accurately because they remain connected by heterochromatic tethers. A recent study examined female meiosis in the closely related species and , and found a nearly twofold difference in the mean distance the obligately nonexchange dot chromosomes were separated during Prometaphase. That study proposed two speculative hypotheses for this difference, the first being the amount of heterochromatin in each species, and the second being the species' differing tolerance for common inversions in natural populations. We tested these hypotheses by examining female meiosis in 12 additional species. While neither hypothesis had significant support, we did see 10-fold variation in dot chromosome sizes, and fivefold variation in the frequency of chromosomes out on the spindle, which were both significantly correlated with chromosome separation distances. In addition to demonstrating that heterochromatin abundance changes chromosome behavior, this implies that the duration of Prometaphase chromosome movements must be proportional to the size of the element in these species. Additionally, we examined , a species that lacks a free dot chromosome. We observed that chromosomes still moved out on the meiotic spindle, and the element was always positioned closest to the spindle poles. This result is consistent with models where one role of the dot chromosomes is to help organize the meiotic spindle.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202005PMC
http://dx.doi.org/10.1534/g3.120.400867DOI Listing

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