Arc Institute

Arc Institute

@arcinstitute.org

A full-stack institute for AI and biology research.

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Much of the functional biology encoded in genomes remains hidden in noncoding DNA. In a preprint out today, Patrick Hsu and team introduce COMPASS, a genomic language model-based approach to systematically map this underexplored sequence space.

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To explore the atlas at scale, the team deployed AI agents to develop analyses and investigate biological hypotheses under researcher guidance. They identified candidate divergent riboswitches, ribozymes, and previously uncharacterized PhoH2-associated RNAs that existing annotation methods missed.

Much of the functional biology encoded in genomes remains hidden in noncoding DNA. In a preprint out today, Patrick Hsu and team introduce COMPASS, a genomic language model-based approach to systematically map this underexplored sequence space.

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Periodicity in Evo-PIN token entropies revealed the internal architecture of tandem repeat arrays. The pattern recovered guide arrays alongside their cognate effector proteins from sequence alone, and nominated new repeat architectures that don't belong to any known RNA-guided system.

COMPASS also uncovered diversity within known RNA families. Across the 32,190 predicted bridge RNAs analyzed, 19% had longer predicted DNA recognition sequences than the characterized IS621 system, identifying variants that may confer greater specificity for genome engineering.

Much of the functional biology encoded in genomes remains hidden in noncoding DNA. In a preprint out today, Patrick Hsu and team introduce COMPASS, a genomic language model-based approach to systematically map this underexplored sequence space.

The team fine-tuned Evo 2 on 750M prokaryotic intergenic sequences to develop Evo-PIN, which captures shared features of noncoding RNAs beyond sequence similarity. COMPASS used these representations to cluster 376M sequences into 5.14M clusters without sequence alignment or prior annotations.

Fewer than 1% of COMPASS clusters contained known ncRNA annotations, highlighting the extent of unexplored sequence diversity. By combining conserved RNA structures with neighboring gene analysis, the team identified 20,149 clusters of candidate structured RNAs with nominated protein partners.

Our cells carry the same DNA, but how this DNA is interpreted differs wildly from cell to cell. In a new preprint, Science Fellow Jingtian Zhou and team introduce Bolero, a model conditioned on cell state that predicts chromatin accessibility and expression from DNA alone.

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Trained only on human data, Bolero's AP-1 model correctly predicted enhancer activity in mouse and macaque neurons it never saw in training. In effect, Bolero turns genome sequence into a queryable map of cell-state-specific regulation across cell types, activity states, and species.

Our cells carry the same DNA, but how this DNA is interpreted differs wildly from cell to cell. In a new preprint, Science Fellow Jingtian Zhou and team introduce Bolero, a model conditioned on cell state that predicts chromatin accessibility and expression from DNA alone.

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The team gave Bolero a dial for AP-1 activity, a per-cell score that conditions the model alongside cell state. Turning this dial up in a virtual simulation, Bolero predicted the unique ways that specific cells changed their DNA accessibility up to 29x better than a motif scan.

It found that different transcription factors team up with AP-1 depending on cell type, and the exact spacing matters. FOX motifs boost the response most when they sit 4 base pairs from AI-1, and each partner motif has its own preferred spacing.

Our cells carry the same DNA, but how this DNA is interpreted differs wildly from cell to cell. In a new preprint, Science Fellow Jingtian Zhou and team introduce Bolero, a model conditioned on cell state that predicts chromatin accessibility and expression from DNA alone.

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That embedding comes from Bolero-10M, a new atlas of 10M+ single cells spanning the human brain and body, development and aging, and multiple species. This lets Bolero predict regulation for cell states it's never directly seen.

To test Bolero’s capability, the team gave it a puzzle: the same neural-activity signal (AP-1) hits many neuron types at once. But while these neurons get an identical signal, they respond completely differently. Why could this be?

Our cells carry the same DNA, but how this DNA is interpreted differs wildly from cell to cell. In a new preprint, Science Fellow Jingtian Zhou and team introduce Bolero, a model conditioned on cell state that predicts chromatin accessibility and expression from DNA alone.

Bolero takes two inputs: the raw DNA sequence, and a "cell-state embedding" describing cell identity. Rather than just tagging cell type onto the output, the embedding generates custom weights added into the network at every layer. Every cell state gets its own effective network.

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Pythia learns RNA sequence and 2D folding directly, without external structural predictors, so it can pinpoint binding sites driven by structure. In tests on five RBPs, disrupting structures flagged by Pythia weakened binding, while preserving the fold rescued it.

RBPs control RNA splicing, transport, translation, and decay, and their malfunction has been linked to diseases like cancer. Models that can explain, not just predict, how these proteins find their targets give researchers testable hypotheses about this layer of gene regulation.

Hundreds of human tRNA genes form a redundant repertoire for decoding the genetic code. But does redundancy imply functional equivalence? A pan-cancer in vivo CRISPRi atlas from @genophoria.bsky.social and Vijay Ramani at @Gladstone Institutes reveals a structured landscape of tRNA dependencies.

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The changes were coordinated across cancer cell lines, revealing tRNA isoacceptors associated with tumor-related adaptation. Distinct codon usage preferences of proliferation- and tumor stress-associated programs provided further biological context.

Hundreds of human tRNA genes form a redundant repertoire for decoding the genetic code. But does redundancy imply functional equivalence? A pan-cancer in vivo CRISPRi atlas from @genophoria.bsky.social and Vijay Ramani at @Gladstone Institutes reveals a structured landscape of tRNA dependencies.

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Are tRNA requirements fixed, or shaped by where cells grow? To find out, the team compared matched CRISPRi screens during tumor growth in vivo and cell culture in vitro.

The same cancer cells showed extensively reorganized tRNA dependencies in tumors versus culture. But dependencies on aminoacyl-tRNA synthetases were much more concordant, highlighting the environmental sensitivity of tRNA requirements.

Hundreds of human tRNA genes form a redundant repertoire for decoding the genetic code. But does redundancy imply functional equivalence? A pan-cancer in vivo CRISPRi atlas from @genophoria.bsky.social and Vijay Ramani at @Gladstone Institutes reveals a structured landscape of tRNA dependencies.

Across 16 cancer cell lines from 7 tissue types, tRNA dependencies in living tumors showed tissue-specific organization. At isodecoder resolution, dependency profiles classified tissue of origin with 80% accuracy.

At isoacceptor level, tRNA dependencies were associated with cellular codon demand, linking the genetic dependencies of the tRNA repertoire to cellular translational demand.

Most perturbation models learn only from experiments. Our new model, PIE, also draws on decades of curated biological knowledge to predict which genes respond to a perturbation, even in biological contexts and for perturbations it has never seen.

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On the Replogle-Nadig dataset, PIE was up to 3.2x better than the strongest baseline at identifying differentially expressed genes, with the biggest gain on unseen perturbations. It still made meaningful predictions when context and perturbation were both unseen.

Most perturbation models learn only from experiments. Our new model, PIE, also draws on decades of curated biological knowledge to predict which genes respond to a perturbation, even in biological contexts and for perturbations it has never seen.

PIE does this by turning public databases (Cellosaurus, NCBI Gene, Gene Ontology, DepMap, PubChem) into inputs. Each gene is represented by its text description, so PIE works across the different gene sets measured in different studies.

Virtual cell models are only as good as the data they learn from. To predict how any cell type responds to a perturbation, models need high-quality causal data generated across contexts, so technical noise doesn't masquerade as biology.

Here's what that looks like in practice. For this year's Virtual Cell Challenge, we ran identical Perturb-seq protocols in six cell lines, profiled 30M+ cells, then selected perturbations with strong (≥80%) median knockdown. Go behind the scenes in this blog post: arcinstitute.org/news/behind-...

arcinstitute.orgGenerating high-quality Perturb-seq data for the 2026 Virtual Cell Challenge | Arc InstituteAt Arc, we believe virtual cell models can fill a critical gap: predicting the effects of genetic mutations, environmental changes, and small molecule treatments in biological systems we cannot readil...

Many important bacterial non-coding RNAs and structural elements remain undiscovered. To help, David Li, Garyk Brixi, Michael Fischbach, @brianhie.bsky.social & team introduce Minerva, which uses a genome language model to predict RNA base pairing, repeats, & other interactions from sequence alone.

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In prophages, Unknown Group 27 reverse transcriptase loci hold arrays of roughly 150nt mcRNA units, diverse in sequence but sharing a predicted structure. Expressed in E. coli, all five systems reverse transcribed the central hairpin of each unit into 50-100nt ssDNA.

Many important bacterial non-coding RNAs and structural elements remain undiscovered. To help, David Li, Garyk Brixi, Michael Fischbach, @brianhie.bsky.social & team introduce Minerva, which uses a genome language model to predict RNA base pairing, repeats, & other interactions from sequence alone.

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Across 150 bacterial genomes, Minerva predicted 62,083 loci carrying at least two neighboring hairpins, and 70.2% of those sit outside existing annotations. The full scan took 100 minutes on one H100.

In Pseudomonas, the TwoAYGGAY RNA family extends well past its Rfam annotation, with three further hairpins and a 3’ pseudoknot on an elongated basal stem. A covariance model rebuilt on the Minerva predictions found 16,086 matches across 1,148 of 1,324 strains.

Many important bacterial non-coding RNAs and structural elements remain undiscovered. To help, David Li, Garyk Brixi, Michael Fischbach, @brianhie.bsky.social & team introduce Minerva, which uses a genome language model to predict RNA base pairing, repeats, & other interactions from sequence alone.

For any portion of a genome, Minerva returns a map of which positions pair with which, including pseudoknots and overlapping hairpins that are hard to capture otherwise. Nothing needs to be aligned first, and one pass per region is fast enough to scan a whole genome.

Loss of function for 1 gene can make a cancer cell resist a DNA damage response (DDR) inhibitor, while another gene can make it easy to kill. Arc Core Investigator Luke Gilbert and collaborators mapped both across five DDR inhibitors and found loss of PRDX1 sensitizes cells to all five.

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The team then repeated the screens in PRDX1 knockout cells. Knocking down IREB2, PAX7, or MRGBP restored growth under DNA-PK inhibition and lowered γH2AX. All three lowered labile iron, and chelating iron partly rescued the cells, indicating PRDX1 protects the genome from iron-driven oxidation.

PRDX1 clears hydrogen peroxide that free iron turns into DNA-damaging hydroxyl radicals. This work identifies PRDX1 and its upstream genes as potential druggable targets to pair with DDR inhibitors or to use in cancers already deficient in DNA repair. See in NChemBio: www.nature.com/articles/s41...

nature.comChemogenomic maps reveal a PRDX1-dependent iron–damage axis in the DNA damage response - Nature Chemical BiologyLarge-scale CRISPR dependency mapping reveals 1,000+ genes that modify cellular outcomes to DNA damage response drugs. Loss of PRDX1, acting through a PAX7–MRGBP–IREB2 pathway, broadly sensitized cell...

Loss of function for 1 gene can make a cancer cell resist a DNA damage response (DDR) inhibitor, while another gene can make it easy to kill. Arc Core Investigator Luke Gilbert and collaborators mapped both across five DDR inhibitors and found loss of PRDX1 sensitizes cells to all five.

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Six genes consistently sensitized cells to all inhibitors when repressed. One was PRDX1, a peroxiredoxin that reduces hydrogen peroxide. Knocking it down raised γH2AX and sensitized cells to the PARP, ATR, ATM, and DNA-PK inhibitors.

The team asked whether antioxidants could substitute for PRDX1. Catalase, SOD1, trolox, glutathione, and NAC offered no protection. Relocalizing PRDX3 or PRDX4 from the mitochondria or ER to the cytosol restored resistance, identifying the damaging ROS as nucleocytoplasmic.

Loss of function for 1 gene can make a cancer cell resist a DNA damage response (DDR) inhibitor, while another gene can make it easy to kill. Arc Core Investigator Luke Gilbert and collaborators mapped both across five DDR inhibitors and found loss of PRDX1 sensitizes cells to all five.

The team screened a genome-scale CRISPRi library in A549 lung cancer cells against the PARP inhibitor olaparib and against inhibitors of the repair kinases including ATR, ATM, DNA-PK, and WEE1. They screened each drug on its own as well as combined with olaparib.

More than 1,200 genes made cells more sensitive to a single inhibitor when repressed, and 300+ made them resistant. The olaparib combinations added 300 more sensitizers. All 32 screens are searchable at ddri-screens.gilbertlab.arcinstitute.org