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Ma, X.-Y.

Publications and source records attributed to Ma, X.-Y..

3 recordsLinked to original sources

NPlasmid-seq: Cas9-encoded terminal signatures enable molecule-level nanopore quality control of vector and IVT-template plasmids

Consensus-based plasmid quality control can overlook structural heterogeneity within a preparation. We developed NPlasmid-seq, a Cas9-guided nanopore workflow that encodes sample identity through paired terminal signatures generated at predefined backbone positions, without sample-specific oligonucleotide barcodes. We cleavage-validated 24 sgRNAs. In five representative assigned read bins, each bin showed its strongest sequence agreement with its cognate reference. Contaminant detection was evaluated with a single class-specific classifier applied both to computational read mixtures and to physical DNA mixtures, placing the two designs on a common scale. In computational read mixtures of 5,000 reads, a contaminant was detected in all 20 independent subsamples at each of 0.2%, 0.5%, 1% and 5% abundance and in 13 of 20 subsamples at 0.1%; precision was 1.000 in all 100 subsamples, with no false-positive calls among 493,200 reads from the declared target plasmid. In physical DNA mixtures carried through cleavage, pooled library preparation and sequencing, a contaminant was detected in all six samples prepared at 0.5 mol% input and all six at 1 mol%. Observed read fractions did not distinguish the 0.5 and 1 mol% input levels. Instead, they differed systematically by 4.0-fold between preparation pools, a larger effect than the difference between the two input levels. We therefore interpret the workflow as a detector, not a quantifier, of sub-percent contamination. Read-level analysis identified a recurrent 93-bp deletion in 61.7% of reads from a preparation that had passed consensus-based quality control. Sanger genotyping of 24 colonies identified deletion-type profiles in 10 colonies and intact-type profiles in three. The remaining 11 colonies showed double peaks at the diagnostic locus, consistent with coexistence of both sequence forms within individual clones. In in vitro transcription template plasmids, longer poly(A) tracts were associated with higher multimeric-read fractions. Across ten matched A90 culture pairs, propagation at 30 degree reduced these fractions relative to 37 degree (paired t-test, P = 0.0098). These measurements describe recovered read populations, not absolute molecular abundances. NPlasmid-seq therefore complements consensus validation by revealing sequence and structural heterogeneity within a preparation and by identifying a culture condition associated with a lower multimeric-read fraction.

bioengineering↗

Visualizing single base RNA mutations in living cells through DNA nanostructure mediated amplification

Capturing RNA dynamics in living cells would provide critical insights into transcriptional control and cellular adaptation, but remains technically formidable -- particularly at single-base precision. Here, we introduce a DNA tetrahedron based three-dimensional catalytic hairpin assembly (3D@CHA) nanoplatform that couples target recognition with catalytic activation in a spatially organized framework. Three cascaded hairpins (H-AN, H1, and H2) then enable localized and efficient signal amplification. Without external carriers or transfection, the platform exhibits robust biocompatibility, distinguishing highly homologous insulin I (Ins1) and insulin II (Ins2) mRNAs in living cells and tracking their redistribution and intercellular transfer during metabolic changes. Introducing a single-base mismatch site into H1 and coupling it with a Forster resonance energy transfer (FRET) readout yielded a KRAS-3D@CHA probe capable of detecting KRASG12D mutations at the RNA level with single-base resolution. This platform establishes a programmable framework for precise RNA imaging and mutation discrimination, opening new avenues for RNA-level diagnostics and precision oncology.

cell biology↗

A neuroendocrine principle: Pancreatic islets actively shape sympathetic innervation

Survival critically depends on maintaining blood glucose levels to provide essential energy, especially during emergencies such as the fight-or-flight response, when timely glucose control via neural integration is vital. However, pancreatic islets constitute only a small fraction of the pancreas and are dispersed throughout the organ, raising the fundamental question of how the nervous system coordinates synchronized control of multiple islets. Using whole-organ clearing and 3D imaging, we mapped pancreatic sympathetic innervation, revealing specialized anatomical integration between sympathetic nerves and islets. Transplanted islets intrinsically attracted sympathetic nerves independent of their native environment. Chronic islet injury disrupted sympathetic innervation and markedly impaired nerve regeneration after denervation. Sympathetic denervation markedly elevated islet-derived Reg2 and Reg3{beta}; administration of these proteins accelerated sympathetic regeneration and improved islet graft function. Our findings identify an islet-sympathetic architecture actively maintained by islets, uncovering an endocrine-driven mechanism for neural regulation, highlighting Reg2 and Reg3{beta} as therapeutic candidates for diabetes management.

neuroscience↗