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Doyle, W. C.

Publications and source records attributed to Doyle, W. C..

2 recordsLinked to original sources

Mountable miniature microphones to identify and assign mouse ultrasonic vocalizations

Vocal communication is a major component of animal social behavior. Vocalizations can be learned or innate, and can convey a variety of signals, including territorial limits, the presence of predators, or courtship intent. Mouse ultrasonic vocalizations (USVs) are a promising model in which to study mammalian vocal production circuits. While mouse USVs are innate, mice still show complex vocal behavior, including production of structured song composed of multiple syllable types and the ability to modify their vocal rate and syllable repertoire based on social conditions. Though in courtship interactions male mice produce the majority of the emitted USVs, female mice are capable of emitting USVs. In order to study the underlying mechanisms of vocal production in freely behaving pairs of mice, it is necessary to identify the individual responsible for each syllable in group settings. Previous methods to identify the source of an individual USVs have used high-density microphone arrays and triangulation methods, which involve the use of multiple costly microphones and require implementation of complex computational methods. Here we identified, developed, and used an inexpensive, mountable, ultrasound-sensitive miniature-microphone system to record and identify USVs from individual mice during dual socializing behavior. Our system includes custom circuit boards that can be fitted to individual mice and connected to a variety of existing USV recording systems. We found that these miniature microphones reliably detected mouse USVs, and that a high percentage (90%) of vocalizations could be attributed to a specific animal in a vocalizing pair based on the relative amplitude differences alone. This simple readout method avoids the implementation of complicated triangulation methods. By pairing this method with simultaneous video recording and automated animal body part and identity tracking, we were able to study and describe the broader courtship behavioral landscape, in which USV production is one component. These results offer a promising, low-cost, and simple method that researchers can implement to study the social vocal communication between at least pairs of vocalizing mice.

animal behavior and cognition↗

Splicing modulators impair DNA damage response and induce killing of cohesin-mutant MDS/AML

Splicing modulation is a promising treatment strategy pursued to date only in splicing-factor mutant cancers; however, its therapeutic potential is poorly understood outside of this context. Like splicing factors, genes encoding components of the cohesin complex are frequently mutated in cancer, including myelodysplastic syndromes (MDS) and secondary acute myeloid leukemia (AML), where they are associated with poor outcomes. Here, we show that cohesin mutations are biomarkers of sensitivity to drugs targeting the splicing-factor SF3B1 (H3B-8800 and E-7107). We identify drug-induced alterations in splicing and corresponding reduced gene expression of a large number of DNA repair genes, including BRCA1 and BRCA2, as the mechanism underlying this sensitivity in cell line models, primary patient samples and patient-derived xenograft (PDX) models of AML. We find that DNA damage repair genes are particularly sensitive to exon skipping induced by SF3B1 modulators given their long length and large number of exons per transcript. Furthermore, we demonstrate that treatment of cohesin-mutant cells with SF3B1 modulators not only results in impaired DNA damage response and accumulation of DNA damage, but it significantly sensitizes cells to subsequent killing by PARP inhibitors and chemotherapy, and leads to improved overall survival of PDX models of cohesin-mutant AML in vivo. Our findings expand the potential therapeutic benefits of SF3B1 splicing modulators to include cohesin-mutant MDS and AML, and we propose this as a broader strategy for therapeutic targeting of other DNA damage-repair deficient cancers. One Sentence SummaryWe identify an unexpected effect of SF3B1 splicing inhibitors on regulation of DNA damage repair genes and show efficacy of combination treatment in cohesin-mutant MDS and AML.

cancer biology↗