Biology subjects

Kao, D.

Publications and source records attributed to Kao, D..

6 recordsLinked to original sources

bioRxiv2025

Daple-FLT3 (CCDC88C-FLT3) gene fusion requires the coiled-coil domain for maximal activation and pericentrosomal localization

Gene fusions are stable protein products often occurring from chromosomal rearrangements. These chimeric proteins typically contain distinct molecular entities from each parent gene, and thus, create a product with altered or aberrant function. Gene fusions are frequently found in cancers, including Leukemia. Here, we characterize the kinase activity and subcellular distribution of the Daple-FLT3 (CCDC88C-FLT3) fusion oncoprotein--a rare, but recurrent gene fusion found in patients with hematological malignancies. The protein contains the FLT3 kinase domain and is activated without ligand stimulation. This leads to activation in STAT5a, AKT, and MAPK signaling, which can be modulated by the tyrosine kinase inhibitors (TKIs) sorafenib, quizartinib, and to a lesser degree, imatinib. Moreover, fusion of this kinase domain to Daple facilitates its localization to the pericentrosomal space and enhances kinase activation. These findings provide evidence that targeting Daple-FLT3 outside of its kinase domain may be a complementary approach with TKI therapy. Key PointsO_LIDaple-FLT3 fusion proteins contain a constitutively active kinase domain, activating distinct signaling molecules in cells C_LIO_LICoiled-coil domain on Daple is dispensable for kinase activation, but necessary for maximal activation C_LI

cancer biology↗

bioRxiv2021

Development of an oral swab based microbiome test for the detection of feline dental disease

Variations in the microbial composition of the mouth (the oral microbiome) have known associations with dental and systemic disease. While this is relatively well understood in humans, research on this topic in companion animals, and in cats in particular, has been limited. In this study, we used oral microbiome data obtained from shotgun metagenomic sequencing of 38,000 cats (data gathered through a direct-to-consumer cat DNA testing platform) to reveal the staggering diversity of the feline oral microbiome, identifying 8,344 microbial species across the entire cohort. We used a subset of these data points (6,110 cats) to develop a feline dental health test able to assess a cats risk of having periodontal disease, tooth resorption and halitosis based on their oral microbiome. After filtering out classified microbial reads with low abundance, we were able to detect 606 microbes in a single cats oral microbiome, identifying not just bacteria, but also viruses, fungi, archaea and protozoa. Due to the shortage of available published research on the microbial signature of tooth resorption and halitosis in cats, we used our periodontal disease feline cohort (n=570) to validate our approach. We observed microbial compositional abundance trends consistent with previously reported findings from feline, canine and human studies on periodontal disease. We used compositional abundance-based statistical methods relying on pairwise log-ratio (PLR) transformation to identify microbes significantly correlated with each of the three dental conditions of interest. We identified a set of 27 microbes that are predictive for all three dental conditions, as well as microbes specifically predictive of periodontal disease, tooth resorption or halitosis. We used the compositional abundance profiles of predictive microbes to develop a risk score based model assessing the probability that a cat is suffering from each of the three dental conditions. The model had highest sensitivity for halitosis (72%) and highest specificity for tooth resorption (78%). Lastly, we observed relatively consistent dental disease risk profiles when we compared data from sample collection methods targeting the whole mouth versus those targeting the gum line specifically. In contrast, samples collected in triplicates from the same cats using a sampling method targeting the whole mouth showed more variation in the generated risk profiles. This was likely due to a failure to consistently collect sufficient sample material from areas of the mouth where microbes relevant to dental pathology would be found in highest amounts (i.e., the gum line). For this reason, we have modified the tests instructions to emphasize the importance of targeting the gum line during sample collection. Regular at home or in clinic screening with the feline dental health test described in this study has the potential to facilitate early detection and prevention of dental disease.

genomics↗

bioRxiv2020

Fecal microbiota transplantation efficacy for Clostridium difficile infection: A trans-kingdom battle between donor and recipient gut microbiomes

Fundamental restoration ecology and community ecology theories can help us better understand the underlying mechanisms of fecal microbiota transplantation (FMT) and to better design future microbial therapeutics for recurrent Clostridium difficile infections (rCDI) and other dysbiosis-related conditions. In a single cohort study, stool samples were collected from donors and rCDI patients one week prior to FMT (pre-FMT) as well as from patients one week following FMT (post-FMT). Using metagenomic sequencing and machine learning methods, our results suggested that the FMT outcome is not only dependent on the ecological structure of the recipients, but also the interactions between the donor and recipient microbiomes, both at the taxonomical and functional levels. Importantly, we observed that the presence of specific bacteria in donors (Clostridiodes spp., Desulfovibrio spp., Odoribacter spp. and Oscillibacter spp.) and the absence of specific fungi (Yarrowia spp.) and bacteria (Wigglesworthia spp.) in recipients prior to FMT could accurately predict FMT success. Our results also suggested a series of interlocked mechanisms for FMT success, including the repair of the disturbed gut microbial ecosystem by transient colonization of nexus species followed by secondary succession of bile acid metabolizers, sporulators, and short chain fatty acid producers. Therefore, a better understanding of such mechanisms can be fundamental key elements to develop adaptive, personalized microbial-based strategies for the restoration of the gut ecosystem. ImportanceThere have been a number of studies focusing on understanding the underlying mechanisms in FMT treatment, which can accordingly be used for the optimization of future treatments. However, the current scientific lens has mainly had a uni-kingdom major focus on bacteria, leading to the proposition of the existence of FMT "super-donors". On the contrary, our preliminary study here suggests that FMT is not necessarily a one stool fits all approach and that donor-recipient cross-kingdom microbiota interactions, along with their short-term fluctuations in the gut, bring profound implications in FMT success. The results also conceptualize a series of interlocked mechanisms for FMT success, including first repairing the disturbed gut microbial ecosystem by transient species, followed by secondary succession of indigenous or exogenous bile acid metabolizers, sporulators, and short chain fatty acid producers.

microbiology↗

bioRxiv2019

The neuropeptide Drosulfakinin regulates social isolation-induced aggression in Drosophila

Social isolation strongly modulates behavior across the animal kingdom. We utilized the fruit fly Drosophila melanogaster to study social isolation-driven changes in animal behavior and gene expression in the brain. RNA-seq identified several head-expressed genes strongly responding to social isolation or enrichment. Of particular interest, social isolation downregulated expression of the gene encoding the neuropeptide Drosulfakinin (Dsk), the homologue of vertebrate cholecystokinin (CCK), which is critical for many mammalian social behaviors. Dsk knockdown significantly increased social isolation-induced aggression. Genetic activation or silencing of Dsk neurons each similarly increased isolation-driven aggression. Our results suggest a U-shaped dependence of social isolation-induced aggressive behavior on Dsk signaling, similar to the actions of many neuromodulators in other contexts.\n\nData availabilityThe raw sequence data from RNA-seq experiments has been deposited into the Sequence Read Archive (https://www.ncbi.nlm.nih.gov/sra) with accession number: PRJNA481582. Supplementary files and figures accompany this article.

neuroscience↗

bioRxiv2017

MLL3/4 Prevents Stem Cell Hyperplasia And Controls Differentiation Programs In A Planarian Cancer Stem Cell Model

Currently, little is known about the evolution of epigenetic regulation in animal stem cells. Using the planarian stem cell system to investigate the role of the COMPASS family of MLL3/4 histone methyltransferases, we demonstrate that their role as tumour suppressors in stem cells is conserved over a large evolutionary distance in animals. This also suggested the potential conservation of a genome wide epigenetic regulation program in animal stem cells, so we assessed the regulatory effects of Mll3/4 loss of function by performing RNA-seq and ChIP-seq on the G2/M planarian stem cell population, part of which contributes to the formation of outgrowths. We find many oncogenes and tumour suppressors among the affected genes that are therefore likely candidates for mediating MLL3/4 tumour suppression function in mammals, where little is known about in vivo regulatory targets. Our work demonstrates conservation of an important epigenetic regulatory program in animals and highlights the utility of the planarian model system for studying epigenetic regulation.

developmental biology↗

bioRxiv2017

Epigenetic analyses of the planarian genome reveals conservation of bivalent promoters in animal stem cells.

Planarian flatworms have an indefinite capacity to regenerate missing or damaged body parts owing to a population of pluripotent adult stems cells called neoblasts (NBs). Currently, little is known about the importance of the epigenetic status of NBs and how histone modifications regulate homeostasis and cellular differentiation. We have developed an improved and optimized ChIP-seq protocol for NBs in Schmidtea mediterranea and have generated genome-wide profiles for the active marks H3K4me3 and H3K36me3, and suppressive marks H3K4me1 and H3K27me3. The genome-wide profiles of these marks were found to correlate well with NB gene expression profiles. We found that genes with little transcriptional activity in the NB compartment but which switch on in post-mitotic progeny during differentiation are bivalent, being marked by both H3K4me3 and H3K27me3 at promoter regions. In further support of this hypothesis bivalent genes also have a high level of paused RNA Polymerase II at the promoter-proximal region. Overall, this study confirms that epigenetic control is important for the maintenance of a NB transcriptional program and makes a case for bivalent promoters as a conserved feature of animal stem cells and not a vertebrate specific innovation. By establishing a robust ChIP-seq protocol and analysis methodology, we further promote planarians as a promising model system to investigate histone modification mediated regulation of stem cell function and differentiation.

developmental biology↗