Current Biology最新文献

Theory predicts that spatial modular networks contain the propagation of local disturbances, but field experimental tests of this hypothesis are lacking. We combined a field experiment with a metacommunity model to assess the role of modularity in buffering the spatial spread of algal turfs in three replicated canopy-dominated macroalgal networks. Experimental networks included three modules where plots with intact canopy cover (nodes) were connected through canopy-thinned corridors. The local perturbation consisted of removal of the canopy and understory species from four nodes within a single module to enable the establishment of algal turfs, which could then spread vegetatively to other untouched nodes through the canopy-thinned links. Results show that algal turfs invade mainly untouched nodes in the perturbed module, in agreement with the hypothesis that modularity can effectively constrain the spread of a spatial perturbation. The metacommunity model supports the empirical findings, illustrating greater resistance to perturbations of modular than random macroalgal canopy networks and making alternative explanations for the observed results unlikely. Evidence that the buffering effect of modularity can operate in natural environmental conditions has important implications for designing more robust networks of protected areas and less-fragile human-dominated fragmented landscapes.

Animals need to rapidly learn to recognize and avoid predators. This ability may be especially important for young animals due to their increased vulnerability. It is unknown whether, and how, nascent vertebrates are capable of such rapid learning. Here, we used a robotic predator-prey interaction assay to show that 1 week after fertilization-a developmental stage where they have approximately 1% the number of neurons of adults-zebrafish larvae rapidly and robustly learn to recognize a stationary object as a threat after the object pursues the fish for ∼1 min. Larvae continue to avoid the threatening object after it stops moving and can learn to distinguish threatening from non-threatening objects of a different color. Whole-brain functional imaging revealed the multi-timescale activity of noradrenergic neurons and forebrain circuits that encoded the threat. Chemogenetic ablation of those populations prevented the learning. Thus, a noradrenergic and forebrain multiregional network underlies the ability of young vertebrates to rapidly learn to recognize potential predators within their first week of life.

Visual experience gives rise to persistent theta oscillations in the mouse primary visual cortex (V1) that are specific to the familiar stimulus. Our recent work demonstrated the presence of these oscillations in higher visual areas (HVAs), where they are synchronized with V1 in a context-dependent manner. However, it remains unclear where these unique oscillatory dynamics originate. To investigate this, we conducted paired extracellular electrophysiological recordings in two visual thalamic nuclei (dorsal lateral geniculate nucleus [dLGN] and lateral posterior nucleus [LP]), the retrosplenial cortex (RSC), and the hippocampus (HPC). Oscillatory activity was not found in either of the thalamic nuclei, but a sparse ensemble of oscillating neurons was observed in both the RSC and HPC, similar to V1. To infer functional connectivity changes between the brain regions, we performed directed information analysis, which indicated a trend toward decreased connectivity in all V1-paired regions, with a consistent increase in V1 → V1 connections, suggesting that the oscillations appear to initiate independently within V1. Lastly, complete NMDA lesioning of the HPC did not abolish theta oscillations in V1 that emerge with familiarity. Altogether, these results suggest that (1) theta oscillations do not originate in the thalamus; (2) RSC exhibits theta oscillations, which may follow V1 given the temporal delay present; and (3) the HPC had a sparse group of neurons, with theta oscillations matching V1; however, lesioning suggests that these oscillations emerge independent of each other. Overall, our findings pave the way for future studies to determine the mechanisms by which diverse inputs and outputs shape this memory-related oscillatory activity in the brain.

Transitioning into and out of dormancy is a crucial survival strategy for many organisms. In unicellular cyanobacteria, surviving nitrogen-starved conditions involves tuning down their metabolism and reactivating it once nitrogen becomes available. Glucose-6-phosphate dehydrogenase (G6PDH), the enzyme that catalyzes the first step of the oxidative pentose phosphate (OPP) pathway, plays a key role in this process. G6PDH is produced at the onset of nitrogen starvation but remains inactive in dormant cells, only to be rapidly reactivated when nitrogen is restored. In this study, we investigated the mechanisms underlying this enzymatic regulation and found that G6PDH inactivation is primarily due to the accumulation of inhibitory metabolites. Moreover, our findings demonstrate that metabolite-level regulation is the driving force behind the resuscitation program. This study highlights the critical importance of metabolite-level regulation in ensuring rapid and precise enzymatic control, enabling microorganisms to swiftly adapt to environmental changes and undergo developmental transitions.

Ancient vomeronasal receptor type-1 (ancV1R), a putative vomeronasal receptor, is highly conserved across a wide range of vertebrates and is expressed in the majority of vomeronasal sensory neurons, co-expressing with canonical vomeronasal receptors, V1Rs and V2Rs. The pseudogenization of ancV1R is closely associated with vomeronasal organ (VNO) degeneration, indicating its critical role in pheromone sensing. However, the specific role of ancV1R remains unknown. In this study, to elucidate the function of ancV1R, we conducted phenotypic analyses of ancV1R-deficient female mice. Behavioral analyses showed that ancV1R-deficient females exhibited rejective responses toward male sexual behavior and displayed no preference for male urine. Physiological analyses demonstrate that the loss-of-function mutation of ancV1R reduced VNO response to various pheromone cues, including male urine, the sexual enhancing pheromone exocrine gland-secreting peptide 1 (ESP1), and β-estradiol 3-sulfate. Pre-exposure to ESP1 did not overcome the rejection behavior caused by ancV1R deficiency. Analysis of neural activity in the vomeronasal system revealed increased responses in the medial amygdala and posteromedial cortical amygdala of mutant females upon contact with males but not in response to male urine alone. Additionally, upon male contacts, ancV1R-deficient females exhibited increased neural activity in the lateral septum, a stress-associated brain region, along with elevated stress hormone levels. Such effects were not observed in females exposed solely to male urine. These findings suggest that, in females, ancV1R facilitates VNO responses to pheromone stimuli and plays a crucial role in perceiving males as mating partners. The absence of ancV1R results in failure of male perception, leading to abnormal sexual behaviors and stress responses upon male contact.

Anaphase is tightly controlled spatiotemporally to ensure proper separation of chromosomes.^1,2,3 The mitotic spindle, the self-organized microtubule structure driving chromosome segregation, scales in size with the available cytoplasm.^4,5,6,7 Yet, the relationship between spindle size and chromosome movement remains poorly understood. Here, we address this relationship during the cleavage divisions of the Drosophila blastoderm. We show that the speed of chromosome separation gradually decreases during the four nuclear divisions of the blastoderm. This reduction in speed is accompanied by a similar reduction in spindle length, ensuring that these two quantities are tightly linked. Using a combination of genetic and quantitative imaging approaches, we find that two processes contribute to controlling the speed at which chromosomes move in anaphase: the activity of molecular motors important for microtubule depolymerization and sliding and the cell cycle oscillator. Specifically, we found that the levels of multiple kinesin-like proteins important for microtubule depolymerization, as well as kinesin-5, contribute to setting the speed of chromosome separation. This observation is further supported by the scaling of poleward flux rate with the length of the spindle. Perturbations of the cell cycle oscillator using heterozygous mutants of mitotic kinases and phosphatases revealed that the duration of anaphase increases during the blastoderm cycles and is the major regulator of chromosome velocity. Thus, our work suggests a link between the biochemical rate of mitotic exit and the forces exerted by the spindle. Collectively, we propose that the cell cycle oscillator and spindle length set the speed of chromosome separation in anaphase.

Flavor is the quintessential multisensory experience, combining gustatory, retronasal olfactory, and texture qualities to inform food perception and consumption behavior. However, the computations that govern multisensory integration of flavor components and their underlying neural mechanisms remain elusive. Here, we use rats as a model system to test the hypothesis that taste and smell components of flavor are integrated in a reliability-dependent manner to inform hedonic judgments and that this computation is performed by neurons in the primary taste cortex. Using a series of two-bottle preference tests, we demonstrate that hedonic judgments of taste + smell mixtures are a weighted average of the component judgments, and that the weight of the components depends on their relative reliability. Using extracellular recordings of single-neuron spiking and local field potential activity in combination with decoding analysis, we reveal a correlate of this computation in gustatory cortex (GC). GC neurons weigh bimodal taste and smell inputs based on their reliability, with more reliable inputs contributing more strongly to taste + smell mixture responses. Input reliability was associated with less variable responses and stronger network-level synchronization in the gamma band. Together, our findings establish a quantitative framework for understanding hedonic multisensory flavor judgments and identify the neural computations that underlie them.

Approaching threats are perceived through visual looming, a rapid expansion of an image on the retina. Visual looming triggers defensive responses such as freezing, flight, turning, or take-off in a wide variety of organisms, from mice to fish to insects.^1,2,3,4 In response to looming, flies perform rapid evasive turns known as saccades.⁵ Saccades can also be initiated spontaneously to change direction during flight.^6,7,8,9 Two types of descending neurons (DNs), DNaX and DNb01, were previously shown to exhibit activity correlated with both spontaneous and looming-elicited saccades in Drosophila.^10,11 As they do not receive direct input from the visual system, it has remained unclear how visually elicited flight turns are controlled by the nervous system. DNp03 receives input from looming-sensitive visual projection neurons and provides output to wing motor neurons^12,13 and is therefore a promising candidate for controlling flight saccades. Using whole-cell patch-clamp recordings from DNp03 in head-fixed flying Drosophila, we showed that DNp03 responds to ipsilateral visual looming in a behavioral-state-dependent manner. We further explored how DNp03 activity relates to the variable behavioral output. Sustained DNp03 activity, persisting after the visual stimulus, was the strongest predictor of saccade execution. However, DNp03 activity alone cannot fully explain the variability in behavioral responses. Combined with optogenetic activation experiments during free flight, these results suggest an important but not exclusive role for DNp03 in controlling saccades, advancing our understanding of how visual information is transformed into motor commands for rapid evasive maneuvers in flying insects.

In vivo functions of the septin and actin cytoskeletons are closely intertwined, yet the mechanisms underlying septin-actin crosstalk have remained poorly understood. Here, we show that the yeast-bud-neck-associated Fes/CIP4 homology Bar-amphiphysin-Rvs (F-BAR) protein suppressor of yeast profilin 1 (Syp1)/FCHo uses its intrinsically disordered region (IDR) to directly bind and bundle filamentous actin (F-actin) and to physically link septins and F-actin. Interestingly, the only other F-BAR protein found at the neck during bud development, Hof1, has related activities and also potently inhibits the bud-neck-associated formin Bnr1. However, we find that Syp1 enhances rather than inhibits Bnr1-mediated actin assembly and fully overcomes Hof1-mediated inhibition of Bnr1. Further, during bud development, Syp1 and Hof1 show reciprocal patterns of arrival and departure from the bud neck, and in vitro Syp1 and Hof1 compete for septin binding. Together, our observations suggest that as the bud grows, the relative levels of these two F-BAR proteins at the bud neck invert, driving changes in septin organization, septin-actin linkage, and formin activity. More broadly, our findings expand the functional roles of Syp1/FCHo family proteins and our understanding of the working relationships among F-BAR proteins in cytoskeletal regulation.

The integration of different sensory streams is required to dynamically estimate how our head and body are oriented and moving relative to gravity. This process is essential to continuously maintain stable postural control, autonomic regulation, and self-motion perception. The nodulus/uvula (NU) in the posterior cerebellar vermis is known to integrate canal and otolith vestibular input to signal angular and linear head motion in relation to gravity. However, estimating body orientation and motion requires integrating proprioceptive cues with vestibular signals. Lesion studies demonstrate that the NU is crucial for maintaining postural control, suggesting it could play an important role in combining multimodal sensory input. Using high-density extracellular recordings in rhesus monkeys, we found that the majority of vestibular-sensitive Purkinje cells also encoded dynamic neck proprioceptive input. Furthermore, Purkinje cells generally aligned their directional tuning to vestibular and proprioceptive stimulation such that self-motion encoding was enhanced. The heterogeneous response dynamics among Purkinje cells enabled their population activity to generate head or body motion encoding in the downstream nuclei neurons on which they converge. Strikingly, when we then experimentally altered the orientation of the head relative to the body, Purkinje cells modulated their responses to vestibular stimulation to account for the change in body motion in space. These findings reveal that the NU integrates proprioceptive and vestibular input synergistically to maintain robust postural control.