bioRxiv Science⌕ Search

Biology subjects

Traenkner, D.

Publications and source records attributed to Traenkner, D..

4 recordsLinked to original sources

A Microglial Regulatory Program Linked to Neuropsychiatric Disorders

Hoxb8 is a transcription factor required for the normal function of a specialized microglial population. Loss of Hoxb8 causes compulsive overgrooming and anxiety-like behaviors in mice, with greater severity in females after sexual maturity. However, the Hoxb8-dependent transcriptional program in microglia remains poorly understood. Here, we integrated Hoxb8 chromatin occupancy, transcriptional responses, and chromatin contacts to classify genes by their spatial relationship to Hoxb8 binding. Hoxb8 occupied thousands of genomic regions, but only a subset of associated genes responded transcriptionally. Locally associated, Hoxb8-activated genes were linked to immune signaling and hormone responsiveness, whereas locally associated, Hoxb8-suppressed genes were linked to cell-cycle and genome-maintenance processes. Distally associated genes contributed to neuronal and intercellular communication and were enriched for genes associated with obsessive-compulsive disorder and anxiety. These findings reveal a functionally organized Hoxb8-dependent transcriptional program and identify potential connections between Hoxb8 activity in microglia, hormone responsiveness, intercellular communication, and neuropsychiatric disease risk.

neuroscience↗

PROX1 Controls Cellular Patterning, Innervation and Differentiation in the Mouse Organ of Corti

The organ of Corti is divided into functional compartments responsible for hearing or cochlear amplification. A medial compartment containing inner hair cells innervated by Type I spiral ganglion neurons and a lateral compartment containing outer hair cells innervated by Type II spiral ganglion neurons. Supporting cells also differ, with lateral compartment pillar cells and Deiters cells developing specialized cellular structures to support outer hair cell electromotility. We bred organ of Corti-restricted Prox1 conditional knockout mice to study lateral compartment development because PROX1 is the first transcription factor expressed strictly in lateral compartment supporting cells. In the absence of Prox1, supporting cell numbers increased without corresponding changes in outer hair cells, and they appear incompletely differentiated based on morphological criteria. Outer hair cell number was not impacted but innervation was disrupted with many afferent neurons turning incorrectly towards the cochlear apex. RNAseq revealed no changes in gene expression that could account for the innervation phenotype. Therefore, we propose that PROX1 promotes pillar and Deiters cell differentiation and organization that has secondary effects on innervation but is not required for compartment specification.

developmental biology↗

Genomic Convergence in Hibernating Mammals Elucidates the Genetics of Metabolic Regulation in the Hypothalamus

Elucidating the genetic basis of mammalian metabolism could help define mechanisms central to health and disease. Here, we define conserved cis-regulatory elements (CREs) and programs for mammalian metabolic control. We delineate gene expression and chromatin responses in the mouse hypothalamus for 7 steps of the Fed-to-Fasted-to-Refed (FFR) response process. Comparative genomics of hibernating versus non-hibernating lineages then illuminates cis-elements showing convergent changes in hibernators. Hibernators accumulated loss-of-function effects for specific CREs regulating hypothalamic FFR responses. Multi-omics approaches pinpoint key CREs, genes, regulatory programs, and cell types in the divergence of hibernating and homeothermic lineages. The refeeding period after extended fasting is revealed as one critical period of chromatin remodeling with convergent genomic changes. This genetic framework is a step toward harnessing hibernator adaptations in medicine. One sentence summaryConvergent signals define cis-regulatory mechanisms behind food scarcity responses and hibernator-homeotherm divergence.

genomics↗

Modular Splicing is Linked to Evolution in the Synapse-Specificity Molecule Kirrel3

Kirrel3 is a cell-adhesion molecule that instructs the formation of specific synapses during brain development in mouse and Kirrel3 variants may be risk factors for autism and intellectual disabilities in humans. Kirrel3 is predicted to undergo alternative splicing but brain isoforms have not been studied. Here, we present the first in-depth characterization of Kirrel3 isoform diversity in brain using targeted, long-read mRNA sequencing of mouse hippocampus. We identified 19 isoforms with predicted transmembrane and secreted forms and show that even rare isoforms generate detectable protein in the brain. We also analyzed publicly-available long-read mRNA databases from human brain tissue and found 11 Kirrel3 isoforms that, similar to mouse, encode transmembrane and secreted forms. In mice and humans, Kirrel3 diversity arises from alternative, independent use of protein-domain coding exons and alternative early translation-stop signals. Intriguingly, the alternatively spliced exons appear at branch points in the chordate phylogenetic tree, including one exon only found in humans and their closest living relatives, the great apes. Together, these results validate a simple pipeline for analyzing isoform diversity in genes with low expression and suggest that Kirrel3 function is fine-tuned by alternative splicing and may play a role in brain evolution. Significance StatementKirrel3 is an important molecule for synapse and circuit formation with gene variants that are associated with neurodevelopmental disorders, yet Kirrel3 function remains largely unknown. Here, we report new isoforms of mouse and human Kirrel3, including secreted and transmembrane forms, that suggest a diverse repertoire of Kirrel3 actions. Importantly, we identified a new Kirrel3 exon only present in humans and the other great apes with potential to play an important role in circuit formation unique to these species.

neuroscience↗