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Bei, D.

Publications and source records attributed to Bei, D..

2 recordsLinked to original sources

RNAi-based screen for cuticle pigmentation in Drosophila melanogaster reveals novel regulators of brain dopamine

The dopaminergic system has been extensively studied for its role in behavior and neurological diseases. Despite this, we still know little about how dopamine levels are regulated in vivo. To identify regulators of dopamine, we utilized Drosophila melanogaster cuticle pigmentation as a readout, where dopamine is used as a precursor to melanin. We started by measuring dopamine from known pigmentation mutants (e.g. tan, ebony, black) and then performed an RNAi-based screen to identify new regulators. We found 153 hits, which were enriched for developmental signaling pathways and mitochondria-associated proteins. From 35 prioritized candidates, 11 had an effect on head dopamine levels. Effects on brain dopamine were mild even when the rate-limiting synthesis enzyme Tyrosine hydroxylase (TH) was knocked down, suggesting changes in dopamine levels are tightly regulated in the nervous system. We pursued two of our hits that reduced brain dopamine levels, clueless and mask. Further examination suggests that mask regulates transcription of TH and affects dopamine-dependent sleep patterns. In summary, by studying genes that affect cuticle pigmentation, we were able to identify genes that affect dopamine metabolism as well as a novel regulator of behavior.

neuroscience↗

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

Individuals with autism spectrum disorders (ASD) exhibit an increased burden of de novo variants in a broadening range of genes. We functionally tested the effects of ASD missense variants using Drosophila through humanization rescue and overexpression-based strategies. We studied 79 ASD variants in 74 genes identified in the Simons Simplex Collection and found 38% of them caused functional alterations. Moreover, we identified GLRA2 as the cause of a spectrum of neurodevelopmental phenotypes beyond ASD in eight previously undiagnosed subjects. Functional characterization of variants in ASD candidate genes point to conserved neurobiological mechanisms and facilitates gene discovery for rare neurodevelopmental diseases.

genetics↗