NLM DIR Seminar Schedule
UPCOMING SEMINARS
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Feb. 17, 2026 Zhaohui Liang
Heterogeneous Graph Re-ranking for CLIP-based Medical Cross-modal Retrieval -
Feb. 19, 2026 Jean Thierry-Mieg
On Magic2, an innovative hardware-friendly RNA-seq analyzer -
Feb. 24, 2026 Ajith Viswanathan Asari Pankajam
TBD -
March 3, 2026 Gianlucca Goncalves Nicastro
TBD -
March 5, 2026 Hasan Balci
TBD
RECENT SEMINARS
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Feb. 5, 2026 Lana Yeganova
From Algorithms to Insights: Bridging AI and Topic Discovery for Large-Scale Biomedical Literature Analysis. -
Jan. 29, 2026 Mehdi Bagheri Hamaneh
FastSpel: A simple peptide spectrum predictor that achieves deep learning-level performance at a fraction of the computational cost -
Jan. 22, 2026 Mario Flores
AI Pipeline for Characterization of the Tumor Microenvironment -
Jan. 20, 2026 Anastasia Gulyaeva
Diversity and evolution of the ribovirus class Stelpaviricetes -
Jan. 8, 2026 Won Gyu Kim
LitSense 2.0: AI-powered biomedical information retrieval with sentence and passage level knowledge discovery
Scheduled Seminars on April 1, 2025
In-person: Building 38A/B2N14 NCBI Library or Meeting Link
Contact NLMDIRSeminarScheduling@mail.nih.gov with questions about this seminar.
Abstract:
In prokaryotes, functionally linked genes are typically clustered into operons, which are transcribed into a single mRNA, providing for the coregulation of the production of the respective proteins, whereas eukaryotes generally lack operons. We explored the possibility that some prokaryotic operons persist in eukaryotic genomes after horizontal gene transfer (HGT) from bacteria. Extensive comparative analysis of prokaryote and eukaryote genomes revealed 33 gene pairs originating from bacterial operons, mostly, encoding enzymes of the same metabolic pathways, and represented in distinct clades of fungi or amoebozoa. This amount of HGT is about an order of magnitude less than that observed for the respective individual genes. These operon fragments appear to be relatively recent acquisitions as indicated by their narrow phylogenetic spread and low intron density. In 20 of the 33 horizontally acquired operonic gene pairs, the genes are fused in the respective group of eukaryotes so that the encoded proteins become domains of a multifunctional protein ensuring coregulation and correct stoichiometry. We hypothesize that bacterial operons acquired via HGT initially persist in eukaryotic genomes under a neutral evolution regime, and subsequently are either disrupted by genome rearrangement or undergo gene fusion which is then maintained by selection.