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Liang Wang

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Open access Jul 2026

Biological Continued Pretraining Reshapes the Capability Profile of a Foundation Model Without Catastrophic Forgetting

It is widely assumed that continued pretraining (CPT) on a narrow, out-of-distribution corpus such as raw biological sequence must trade away a general-purpose model’s broad competence — the “alignment tax” or catastrophic-forgetting intuition. We test this directly, without any new training, by re-analyzing three checkpoints from a single lineage of a 26B-parameter Mixture-of-Experts model (Gemma-4-26B-A4B): the instruction-tuned base, the same model after biological CPT (8.7B tokens of DNA, protein, and biomedical text), and after subsequent supervised fine-tuning (SFT). Across three independent capability axes — general knowledge/reasoning (MMLU, ARC, HellaSwag), code generation (MBPP), and biomedical knowledge (BixBench) — we find that biological CPT does not degrade the model; it lifts it: MMLU +13 points, MBPP pass@1 nearly doubles (0.33 →0.63), and BixBench discrimination rises sharply (MCC 0.23 → 0.92). The single measured regression is truthfulness (TruthfulQA 8.8 points), a small and interpretable domain drift. A clean vocabulary-expansion ablation (< 0.4 pt on every general metric) confirms the gains are attributable to CPT, not tokenizer changes. Crucially, subsequent SFT narrows the model back: all three axes fall to near-base levels, revealing a consistent division of labor — CPT re-organizes and lifts the shared capability substrate; SFT cashes it out onto target tasks. We argue this reframes biological sequence not as a competitor for a foundation model’s capacity but as a form of structured scientific data that reshapes its capability profile, and that CPT and SFT should be budgeted as complementary rather than substitutable stages. All checkpoints, evaluation code, and per-example outputs are public. Highlights A training-free re-analysis of one 26B MoE lineage isolates the effect of biological continued pretraining (CPT) from tokenizer changes and from fine-tuning. Biological CPT does not cause catastrophic forgetting; it raises general knowledge (MMLU +13 pts) and code generation (MBPP pass@1 0.33 → 0.63). CPT also makes chain-of-thought reasoning 41% shorter and near-backtrack-free while pre-serving accuracy — an effect invisible to accuracy metrics. A consistent CPT-lifts / SFT-narrows division of labor recurs across four axes, reframing biological sequence as structured scientific data that reshapes a model’s capability profile. The Bigger Picture Adapting a general-purpose AI model to a specialized domain — here, the language of DNA and proteins — is usually assumed to come at a cost: teach it biology and it forgets how to reason about everything else. This “no free lunch” intuition shapes how practitioners budget compute and whether they attempt domain adaptation at all. We test the assumption directly, and without running any new training, by comparing three snapshots of the same model taken before and after biological training. The result overturns the intuition: feeding the model raw biological sequence made it better at general knowledge, at writing code, and even changed how it reasons — producing shorter, more decisive chains of thought without losing accuracy. The gains appear during the sequence-pretraining stage and are partly given back during task-specific fine-tuning, revealing that the two stages play complementary rather than interchangeable roles. This suggests a broader principle for data-centric AI: structured scientific data — biological sequence today, and by extension code, mathematics, and chemistry — is not merely knowledge to be absorbed but a lever that reshapes what a foundation model can do.

Liang Wang · 0 citations
Open access Jul 2026

Asymmetric Structural Transfer Between Natural Language and Biological Foundation Models

Cross-domain transfer is a defining property of foundation models, yet whether such transfer is symmetric across domains remains unknown. Prior work has reported a striking transfer from natural language to biological sequences: language models fine-tuned only on English structural tasks acquire zero-shot protein-homology discrimination. Here we ask the converse and general question—is structural transfer between language and biology directional? —and answer it systematically. We first reproduce forward transfer (language →biology) under controlled conditions, then evaluate the reverse direction (biology →language) across fine-tuning, iso-token continued pretraining, model scaling, multiple biological foundation-model families (ESM-2, ProtBERT), and adversarial synthetic structure tasks. Reverse transfer is consistently weak: it does not exceed matched-token controls, does not scale, and does not generalize. In an architecture-matched 2 × 2 analysis on models with known training data—which eliminates the pretraining-contamination confound that clouds large-model studies—a language model retains far more competence when moved to biology (off-domain drop 0.08) than a biological model retains when moved to language (drop 0.36). Scaling widens rather than closes this gap: language →biology transfer strengthens with size while biology →language transfer decays toward chance, a pattern shared by two independent protein-model families. Our findings establish that shared structural regularities between natural language and biological sequences do not imply symmetric representational transfer, revealing an intrinsic directionality in cross-domain foundation-model learning.

Liang Wang · 0 citations