Molecular biology explores the tiny machinery inside living cells, revealing how genetic instructions are read, copied, and turned into the proteins that keep us alive. This field acts as a bridge between the static code of DNA and the dynamic processes that drive growth, disease, and life itself, offering insights into everything from cellular repair to the development of new medicines.

On Gist.Science, we track every new preprint uploaded to bioRxiv in this category to make these complex discoveries accessible to everyone. Our team processes each submission to provide both clear, plain-language explanations and detailed technical summaries, ensuring you can grasp the core findings without getting lost in dense academic jargon.

Below are the latest molecular biology papers freshly processed from bioRxiv, ready for you to explore and understand.

📄 molecular biology

The HBV basal core promoter mutation confers a replicative advantage and transcriptionally reprograms hepatocytes toward HCC subtypes

This study demonstrates that the Hepatitis B virus basal core promoter (BCP) mutation enhances viral replication and transcriptionally reprograms hepatocytes to activate cancer-related pathways, thereby defining a distinct molecular subtype of hepatocellular carcinoma.

Seifert, L. L., Dangas, G., Chu, H., Yu, Y., Ogata, K., Hong, X., Zhang, M., Zhou, Y., Zou, C., Ramandi, A., Quirk, C. (…)2026-09-23
📄 molecular biology

Mutational screening reveals a cluster of residues within the SARS-CoV-2 nsp1 N-terminus that confers RNA-targeting selectivity

This study identifies two specific clusters of surface-exposed residues within the SARS-CoV-2 nsp1 N-terminal domain that are essential for distinguishing viral mRNA from host mRNA and for triggering mRNA decay, thereby explaining how the virus evades its own translational repression mechanism.

Guillen, J. V., Tokamov, S. A., Glaunsinger, B. A.2026-09-23
📄 molecular biology

Naloxone as mitochondrial phenotype rescuer in a 3D bioprinted LCHADD/VLCADD model

This study demonstrates that the opioid antagonist naloxone rescues mitochondrial morphology and restores vascularization in a 3D bioprinted model of LCHADD/VLCADD by inhibiting NOX2-driven oxidative stress, suggesting its potential as a rescue therapy for metabolic crises in these patients.

Degen, A., Ausserlechner, M., Sturmlehner, V., Ploner, C., Tucci, S., Karall, D., Homaeirad, H., Neumann, L., Hagenbuchn (…)2026-09-22
📄 molecular biology

Positive selection tends to act on exposed extracellular regions and delineate interaction modules targeted by pathogens

This study reveals that positive selection in human proteins predominantly targets exposed extracellular regions and pathogen-interaction interfaces, suggesting that host-pathogen conflicts drive adaptive evolution while identifying these evolutionarily selected residues as promising therapeutic targets.

Dobson, L., Schad, E., Ficho, E., Tantos, A., Szabo, A., Tusnady, G. E., Pancsa, R.2026-09-22
📄 molecular biology

LARP1-DM15/Sgt is a reader for cap-adjacent 2`-O-ribose methylation in TOP ribosomal protein mRNAs required for localization to synapses

This study identifies LARP1-DM15/Sgt as a reader complex that recognizes cap-adjacent 2'-O-ribose methylation (cOMe) on TOP ribosomal protein mRNAs to stabilize them and facilitate their localization to Drosophila synapses, thereby supporting local protein synthesis for sustained synaptic function.

Tian, Y. W., Hadzhiev, Y., Abis, G., Dodel, M., Alard, E., McQuarrie, D., Mardakheh, F. K., Conte, M., Mueller, F., Soll (…)2026-09-18
📄 molecular biology

Impact of hepatitis E virus host- and virus-derived insertions on the antiviral response in primary human hepatocytes

This study demonstrates that hepatitis E virus variants with different hypervariable region (HVR) insertions elicit distinct innate immune responses in primary human hepatocytes, with the HVR duplication variant triggering a significantly weaker antiviral response and suggesting a positive correlation between viral replication and host immune induction.

Schlienkamp, S., Nocke, M. K., Ulrich, R. G., Kinast, V., Steinmann, E., Todt, D.2026-09-17
📄 molecular biology

RNA trans-splicing treatment for Duchenne muscular dystrophy

The study introduces a multi-vector RNA End Joining (REJ) system that utilizes the cell's intrinsic spliceosome to reassemble large therapeutic proteins from split AAV vectors, demonstrating efficient, safe, and effective restoration of dystrophin expression to prevent muscle degeneration in Duchenne muscular dystrophy models.

Hsu, R. H., Williams, C. E., Maier, G., Gullo, M., Lettieri, K., Alvarez, C. J., Hermann, K. J., Kramer, S., Panda, S. (…)2026-09-16
📄 molecular biology

Genome-wide structural variant landscape following HDR-enhanced CRISPR editing in human hematopoietic stem and progenitor cells

This study reveals that while DNA-PK inhibitors moderately increase large on-target deletions in edited human hematopoietic stem and progenitor cells without substantially elevating genome-wide structural variations, the inherent risks of editing-induced structural variations necessitate careful safety assessments for all therapeutic protocols, particularly those involving multiple simultaneous edits.

Cloarec-Ung, F.-M., Sauvageau, G., Sheppard, H. M., Lansdorp, P. M., Knapp, D. J.2026-09-15
📄 molecular biology

A Pmk1-Regulated Mst12-Bip1 Network Coordinates Appressorium Function, Effector Deployment, and Invasive Growth by Magnaporthe oryzae

This study reveals that the Pmk1 MAP kinase orchestrates rice blast infection by regulating a transcriptional network involving the Mst12 and Bip1 factors, which collectively coordinate appressorium function, effector deployment, and invasive growth in *Magnaporthe oryzae*.

Molinari, C., Sahu, N., Ryder, L. S., Yan, X., Geshkovski, V., Nobori, T., Talbot, N. J.2026-09-14