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Is it your fate to tie macramé while drinking coffee and eating sherbet in a minaret? That would be an unusual destiny, but if it turns out to be your kismet, you will owe much to Turkish and Arabic. We borrowed kismet from Turkish in the 1800s, but it ultimately derives from the Arabic qisma, meaning "portion" or "lot." Several other terms in our bizarre opening question (namely, macramé, coffee, sherbet, and minaret) have roots in those languages too. In the case of macramé and minaret, there is a little French influence as well. Coffee and macramé also have Italian relations, and sherbet has an ancestor in a Persian name for a type of cold drink.
The Kismet team has published several articles on the work, most recently in the July/August 2000 issue of IEEE Intelligent Systems. For more information, including video of the robot and technical papers, go to -robotics-group/kismet/kismet.html.
I believe in kismet. And because of kismet, the past year had me sitting in an olive-green W. H. Gunlocke chair, facing my desk in my office, writing a cookbook manuscript about the history of Black ice cream in America. My eyes often wandered to the pinboard above my desk, covered in postcards, photos, milagros, neon-pink Post-its, pastel pushpins, quotes, and reminders of things to do. It was a year of reading books about ice cream, ice, history, and sugar. Many months spent carefully combing the internet for any tidbit of information, and bidding on photos of Black America eating ice cream in the mid-twentieth century as I wondered what I got myself into. This is all out of character for me. Professionally, I identify as a pastry chef, not a writer. Be that as it may, no matter how uncomfortable I was with the writing, I knew these stories had to be told. The voices sat with me, ate with me, and slept with me. Am I a vessel? I often wondered. Or was this just good timing?
Chromatin remodeling proteins of the chromodomain DNA-binding protein family, CHD7 and CHD8, mediate early neurodevelopmental events including neural migration and differentiation. As such, mutations in either protein can lead to neurodevelopmental disorders. How chromatin remodeling proteins influence the activity of mature synapses, however, is relatively unexplored. A critical feature of mature neurons is well-regulated endocytosis, which is vital for synaptic function to recycle membrane and synaptic proteins enabling the continued release of synaptic vesicles. Here we show that Kismet, the Drosophila homolog of CHD7 and CHD8, regulates endocytosis. Kismet positively influenced transcript levels and bound to dap160 and endophilin B transcription start sites and promoters in whole nervous systems and influenced the synaptic localization of Dynamin/Shibire. In addition, kismet mutants exhibit reduced VGLUT, a synaptic vesicle marker, at stimulated but not resting synapses and reduced levels of synaptic Rab11. Endocytosis is restored at kismet mutant synapses by pharmacologically inhibiting the function of histone deacetyltransferases (HDACs). These data suggest that HDAC activity may oppose Kismet to promote synaptic vesicle endocytosis. A deeper understanding of how CHD proteins regulate the function of mature neurons will help better understand neurodevelopmental disorders.
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