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Pitsch, M. J.

Publications and source records attributed to Pitsch, M. J..

2 recordsLinked to original sources

A genetic model of copulatory wounding in Drosophila melanogaster

In the animal kingdom, copulatory wounds occur due to aggressive behavior or injury from the female or male appendages in contact. Copulatory wounds are a source of sexual conflict as the injury can lead to death or infection. In the laboratory, Drosophila melanogaster does not ordinarily exhibit signs of injury during copulation, but here we find can be induced to do so by overexpression of the serine protease, Hayan, in either the male or female fruit fly. Melanin deposits mark sites of injury along the female ventral abdomen and occur following a single copulation event. The male fly mid-legs are the source of injury as they rub against the ventral female abdomen. Surgical removal of the male mid-legs prevents melanization while still permitting mating to occur. Likewise, removal of the right or left mid-leg results in a corresponding loss of melanization on the female abdominal side that lacks the mid-leg contact. Thus, it appears that overexpression of Hayan alters the female and male anatomy to sensitize it to injury during copulation. We show that these copulatory wounds heal similar to a puncture wound via the generation of enlarged multinucleated, polyploid cells. However, the size of the injury dictates the mechanism of healing. The polyploid cells arise solely by cell fusion in response to small injuries (<1,000m2), whereas the endocycle is simultaneously simulated by larger wounds (>3,000m2) to compensate for cell loss. Therefore, we speculate that wound-induced polyploidization may have evolved to repair similar injuries resulting from sexual conflict in nature.

developmental biology↗

Biochemical computation underlying behavioral decision-making

Computations in the brain are broadly assumed to emerge from patterns of fast electrical activity. Challenging this view, we show that a male flys decision to persist in mating, even through a potentially lethal threat, hinges on biochemical computations that enable processing over minutes to hours. Each neuron in a recurrent network measuring time into mating contains slightly different internal molecular estimates of elapsed time. Protein Kinase A (PKA) activity contrasts this internal measurement with input from the other neurons to represent evidence that the networks goal has been achieved. When consensus is reached, PKA pushes the network toward a large-scale and synchronized burst of calcium influx, which we call an eruption. The eruption functions like an action potential at the level of the network, transforming deliberation within the network into an all-or-nothing output, after which the male will no longer sacrifice his life to continue mating. We detail the continuous transformation between interwoven molecular and electrical information over long timescales in this system, showing how biochemical activity, invisible to most large scale recording techniques, is the key computational currency directing a life-or-death decision.

neuroscience↗