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Gruner, H. N.

Publications and source records attributed to Gruner, H. N..

2 recordsLinked to original sources

Robo1 and 2 repellent receptors cooperate to guide facial neuron cell migration and axon projections in the embryonic mouse hindbrain

BackgroundThe facial nerve is necessary for our ability to eat, speak, and make facial expressions. Both the axons and cell bodies of the facial nerve undergo a complex embryonic migration pattern involving migration of the cell bodies caudally and tangentially through rhombomeres, and simultaneously the axons projecting to exit the hindbrain to form the facial nerve.\n\nResultsOur goal in this study was to test the functions of the chemorepulsive receptors Robo1 and Robo2 in facial neuron and axon migration by analyzing genetically marked motor neurons in double mutant mouse embryos through the migration time course, E10.0-E13.5. In Robo1/2 double mutants, axon and cell body migration errors were more severe than in single mutants. Most axons did not make it to their motor exit point, and instead projected into and longitudinally within the floor plate. Surprisingly, some facial neurons had bifurcated axons that either exited or projected into the floor plate. At the same time, a subset of mutant facial cell bodies failed to migrate caudally, and instead shifted into the floor plate.\n\nConclusionsRobo1 and Robo2 have redundant functions to guide multiple aspects of the complex cell migration of the facial nucleus, as well as regulating axon trajectories and suppressing formation of ectopic axons.\n\nBullet pointsO_LIRobo1 and 2 repellent receptors were tested for functions in facial neuron cell body and axon migration in the developing E10.0-E13.5 hindbrain of double mutant mouse embryos.\nC_LIO_LIIn Robo1;Robo2 double mutant embryos, facial motor neuron cell bodies and axons abnormally grew into the hindbrain floor plate, with stronger effects than in single Robo mutants.\nC_LIO_LIMany facial nerve axons abnormally bifurcated, failed to project to their proper exit point, and instead projected longitudinally within the floor plate.\nC_LIO_LIFacial neuron cell body tangential migration was disrupted.\nC_LIO_LIRobo receptor-mediated repulsion is required for proper migration of both facial axon projections and cell body migrations.\nC_LI\n\nFunding was provided to G.S.M. by NIH R01 NS054740, R21 NS077169, and R01 EY025205. Core facilities at the University of Nevada Reno campus are supported by NIH COBREs GM103650 and GM103554, and Nevada INBRE GM103440.

neuroscience

Global accumulation of circRNAs during aging in Caenorhabditis elegans

Circular RNAs (CircRNAs) are a newly appreciated class of RNAs that lack free 5{acute} and 3{acute} ends, are expressed by the thousands in diverse forms of life, and are mostly of enigmatic function. Ostensibly due to their resistance to exonucleases, circRNAs are known to be exceptionally stable. Here, we examined the global profile of circRNAs in C. elegans during aging by performing ribo-depleted total RNA-seq from the fourth larval stage (L4) through 10-day old adults. Using stringent bioinformatic criteria and experimental validation, we annotated 1,166 circRNAs, including 575 newly discovered circRNAs. These circRNAs were derived from 797 genes with diverse functions, including genes involved in the determination of lifespan. A massive accumulation of circRNAs during aging was uncovered. Many hundreds of circRNAs were significantly increased among the aging time-points and increases of select circRNAs by over 40-fold during aging were quantified by qRT-PCR. The age-accumulation of circRNAs was not accompanied by increased expression of linear RNAs from the same host genes. We attribute the global scale of circRNA age-accumulation to the high composition of postmitotic cells in adult C. elegans, coupled with the high resistance of circRNAs to decay. These findings suggest that the exceptional stability of circRNAs might explain age-accumulation trends observed from neural tissues of other organisms, which also have a high composition of post-mitotic cells. Given the suitability of C. elegans for aging research, it is now poised as an excellent model system to determine if there are functional consequences of circRNA accumulation during aging.

genomics