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Camacho, N.

Publications and source records attributed to Camacho, N..

3 recordsLinked to original sources

WATER reveals heterochrony of molecular programs underlies developmental failure caused by minor spliceosome inhibition

The final limb structure reflects coordinated deployment of molecular programs, defined not only by which genes are expressed but when they are activated and silenced across time. Existing omics analyses obscure the temporal unfolding of these programs and conflate program identity with deployment timing by assuming temporal equivalence between conditions. We developed WATER (Weighted Windowed Assignment of Temporal Expression of RNA), a framework that reconstructs temporal gene expression trajectories independently within each condition, enabling direct comparison of temporal program architecture between wild-type and perturbed systems. Applying WATER to U11-null mouse forelimb development revealed that minor spliceosome inhibition redistributes genes across inappropriate temporal trajectories. Minor spliceosome inhibition causes splicing defects in minor intron-containing genes such as the PRC2 component Eed, leading to reduced H3K27me3 deposition and chromatin-transcription divergence. Single-cell RNA sequencing revealed persistence of progenitor states, impaired chondrogenic progression, and p53-dependent apoptotic checkpoint activation. Orthogonal WATER analysis of Eed-knockout stem cells recapitulated key features of chromatin gating failure, including temporal redistribution of skeletal development programs and progenitor state persistence, confirming that Eed loss alone is sufficient to produce temporal program redistribution independently of other splicing defects. Trp53 ablation in U11-null limbs partially rescued distal limb structures without correcting the underlying splicing defects, establishing that checkpoint activation amplifies rather than initiates the timing disruption. The limb retains much of its molecular toolkit but executes it in the wrong order, demonstrating that developmental failure arises from mistimed deployment of intact molecular programs. Thus, temporal program architecture is a fundamental organizing principle of morphogenesis.

developmental biology↗

Subcellular relocalization and nuclear redistribution of the RNA methyltransferases TRMT1 and TRMT1L upon neuronal activation

RNA modifications are dynamic chemical entities that regulate RNA fate, and an avenue for environmental response in neuronal function. However, which RNA modifications may be playing a role in neuronal plasticity and environmental responses is largely unknown. Here we characterize the biochemical function and cellular dynamics of two human RNA methyltransferases previously associated with neurological dysfunction, TRMT1 and its homolog, TRMT1-like (TRMT1L). Using a combination of next-generation sequencing, LC-MS/MS, patient-derived cell lines and knockout mouse models, we confirm the previously reported dimethylguanosine (m 2,2 G) activity of TRMT1 in tRNAs, as well as reveal that TRMT1L, whose activity was unknown, is responsible for methylating a subset of cytosolic tRNA Ala (AGC) isoacceptors at position 26. Using a cellular in vitro model that mimics neuronal activation and long term potentiation, we find that both TRMT1 and TRMT1L change their subcellular localization upon neuronal activation. Specifically, we observe a major subcellular relocalization from mitochondria and other cytoplasmic domains (TRMT1) and nucleoli (TRMT1L) to different small punctate compartments in the nucleus, which are as yet uncharacterized. This phenomenon does not occur upon heat shock, suggesting that the relocalization of TRMT1 and TRMT1L is not a general reaction to stress, but rather a specific response to neuronal activation. Our results suggest that subcellular relocalization of RNA modification enzymes play a role in neuronal plasticity and transmission of information, presumably by addressing new targets.

molecular biology↗

The Healthy Brain Network Biobank: An open resource for transdiagnostic research in pediatric mental health and learning disorders

Technological and methodological innovations are equipping researchers with unprecedented capabilities for detecting and characterizing pathologic processes in the developing human brain. As a result, ambitions to achieve clinically useful tools to assist in the diagnosis and management of mental health and learning disorders are gaining momentum. To this end, it is critical to accrue large-scale multimodal datasets that capture a broad range of commonly encountered clinical psychopathology. The Child Mind Institute has launched the Healthy Brain Network (HBN), an ongoing initiative focused on creating and sharing a biobank of data from 10,000 New York area participants (ages 5-21). The HBN Biobank houses data about psychiatric, behavioral, cognitive, and lifestyle phenotypes, as well as multimodal brain imaging (resting and naturalistic viewing fMRI, diffusion MRI, morphometric MRI), electroencephalography, eye-tracking, voice and video recordings, genetics, and actigraphy. Here, we present the rationale, design and implementation of HBN protocols. We describe the first data release (n = 664) and the potential of the biobank to advance related areas (e.g., biophysical modeling, voice analysis).

neuroscience↗