HomeInVivo Biosystems BlogView from the BenchMistakes and Lessons Learned Part 5: Maintaining Homozygous Cultures/Male Identification

Mistakes and Lessons Learned Part 5: Maintaining Homozygous Cultures/Male Identification


In this five part series we are exploring some common mishaps when working with C. elegans, so you can hopefully avoid them too! Especially since when testing a specific variable (compound, strain, etc.) we want to limit all other variables that may skew results or lead to inaccurate data. In the final installation of this five part series, we ask: is it a problem that I identified several males while prepping for an experiment? What should I do about it?

Males exist in low frequencies under ideal laboratory conditions (≤0.002 for Bristol N2) and although variation exists between Caenorhabditis strains, it is always below 0.5. Identifying males in your C.elegans culture may be an identifier that the population has experienced some degree of stress, or the population has been grown for too many generations that has allowed outcrossing. 

For most experiments, 1-2 males per 1000 hermaphrodites will not heavily skew data and therefore can be picked off of plates once identified. Lifespan experiments are one of the assays that are more sensitive to the presence of males, because the lifespan of a hermaphrodite that has been mated by a male is significantly less than a self-fertilized hermaphrodite. Males are also smaller than hermaphrodites, therefore they should also be removed from experiments where the size of C.elegans is being taken into consideration for phenotype determination. In addition to the smaller size of males, they may also be identified by their behavior. Males will move alongside a hermaphrodite for mating. 

identifying male worms

A video identifying a smaller, male C.elegans.


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