Search bioRxiv⌕ Search

Biology subjects

Geiselman, G. M.

Publications and source records attributed to Geiselman, G. M..

3 recordsLinked to original sources

The phage stress test: a proving ground for genome language models in biological prediction

Reliable biological prediction by AI is most likely to emerge first in the simplest systems with rich datasets and the fastest opportunities for testing and refinement. Phages with small genomes are an ideal testbed. Decades of experimental work have created an unusually information-rich literature benchmark that sits largely outside the sequence repositories typically used to train genome language models (GLMs). Recent work has shown that GLMs such as Evo2 can generate viable whole bacteriophage genomes, demonstrating that genome-scale biological design is possible. The next question is more mechanistic: can such models correctly predict the effects of simple, local sequence changes? Here, we evaluated Evo2 against experimental mutation data from two model phages: the single-stranded RNA phage MS2 and the single-stranded DNA phage {Phi}X174. We first addressed whether Evo2 sequence log-likelihood scores could distinguish viable from nonviable mutations, and then whether models trained on Evo2 embeddings were predictive of function. Across both phages, Evo2 captured expected sequence-level constraints: stop codons were generally penalized, synonymous substitutions had higher likelihood than nonsynonymous substitutions. Evo2 distinguished among synonymous codons in ways only weakly explained by host codon usage. However, for MS2, these capabilities did not translate into robust biological predictions. Specifically, Evo2 {Delta}SLL failed to distinguish functional from nonfunctional mutations in the lysis gene, an overlapping viral region that appears to be a particularly hard test case. In {Phi}X174, performance was stronger but still modest, and much of the apparent signal could be explained by simple covariates such as nonsense mutations, genomic position, and nucleotide distance from the reference. Together, these results introduce phages as a tractable proving ground for stress-testing GLMs against experimentally grounded genotype-to-phenotype tasks. More broadly, they provide a durable framework for identifying what data and model ingredients are required for biologically reliable prediction.

bioinformatics↗

Unfiltered: A rapid method for Agrobacterium-mediated transformation of Basidiomycete and Ascomycete yeasts

Agrobacterium-mediated transformation (AMT) is a critical method for genetic manipulation of non-model fungi, yet it remains a laborious and inefficient technique. When cocultured in acetosyringone-supplemented induction medium, Agrobacterium transfers DNA directly into yeast cells using its virulence machinery. Membrane filters are commonly used to support the co-culture of yeast and Agrobacterium on agar plates, however some reports demonstrate that these filters are unnecessary for specific yeast species. Here we confirm across diverse budding yeasts that membrane filters are not necessary for effective AMT. Concentrating the cells via centrifugation and "spotting" the cell pellet directly onto the induction medium proved effective. This reduces hands-on time to 15 minutes and eliminates filter cost. In the oleaginous yeast, Rhodotorula toruloides, this simplified method increases transformation efficiency by 66% to 2,500 transformants per 106 recipient cells. We further optimized the Agrobacterium:Rhodotorula cell ratio and culture resuspension volume to achieve more than 200,000 CFU per transformation representing a 2-3 fold improvement over previously implemented protocols. This spot-plating method was successfully applied to seven yeast species, including one for which genetic transformation has not previously been reported, Botryozyma nematodophila. This approach highlights the broad applicability of the spot-plating method across diverse yeast systems. Furthermore, this method could facilitate high-throughput transformation workflows that are critical for genome-scale functional studies.

microbiology↗

Genetically refactored Agrobacterium-mediated transformation

Members of Agrobacterium are costly plant pathogens while also essential tools for plant transformation. Though Agrobacterium-mediated transformation (AMT) has been heavily studied, its polygenic nature and its complex transcriptional regulation make identifying the genetic basis of transformational efficiency difficult through traditional genetic and bioinformatic approaches. Here we use a bottom-up synthetic approach to systematically refactor the tumor-inducing plasmid, wherein the majority of AMT machine components are encoded, into a minimal set of genes capable of plant and fungal transformation that is both controllable and orthogonal to its environment. We demonstrate that engineered vectors can be transferred to new heterologous bacteria, enabling them to transform plants. Our reductionist approach demonstrates how bottom-up engineering can be used to dissect and elucidate the genetic underpinnings of complex biological traits, and may lead to the development of strains of bacteria more capable of transforming recalcitrant plant species of societal importance.

microbiology↗