Andreas Hejnol's picture
self portrait
  • E-mailAndreas.Hejnol@uib.no
  • Phone+47 55 58 43 28+47 930 71 870
  • Visitor Address
    Molecular Biology, Thormøhlensgate 55
    5006 Bergen
    523 A2
  • Postal Address
    Postboks 7803
    5020 Bergen

Understanding the evolution of animal biodiversity is one of the major goals in biology. How animals explored new habitats from only being confined to the marine environment and how the body plans diversified is still one of the most tremendous questions to be answered. My group studies a broad range of animal taxa using morphological and molecular tools to unravel the evolution and development of animal organ systems and the evolution of novel cell types. In the “post-genomic age” with its novel and advanced molecular tools we are able to study the connection between the genotype and the phenotype and how the interaction of genes and cells lead to the formation of a fertile adult. The “translation” of the genomic information into a living individual is realised during the process of development. Studying the development of an organism in which a single fertilised cell gives rise to a complex animal is not only fascinating, but is also one of the key processes to study to finally understand the evolution of animal diversity. Furthermore we study how developmental stages adapt to their environment. I investigate the genomic, molecular and cellular foundations of the development of diverse animal groups such as priapulids, acoels, bryozoans, brachiopods, nematomorphs, platyhelminthes, rotifers and nemerteans using the comparative evolutionary approach. My research team combines wet-lab approaches and bioinformatics to a unique ‘hybrid’ approach to gain information from a broad range of animal taxa using species that can be kept in the laboratory and some that are collected from the aquatic environment. My approach using broad taxon sampling instead of being limited to a model system adds to my unique profile and to my visibility in the field. I use advanced microscopical methods such as live 3D-timelapse microscopy (4D-microscopy) and light-sheet microscopy to study developmental processes in detail. I combine this approach with comparative genomics (de novo genome sequencing) and single-cell transcriptomics to identify evolutionary changes in the genes, their regulatory regions and their expression. We follow up on the discoveries with experimentally testing the role of genes with genome editing technologies (CRISPr-Cas9) in the organism. The molecular approaches allow to unravel the genetic framework underlying the formation of cell type diversity and different organ systems, such as the CNS (Marine Neurobiology), the alimentary canal and other mesodermal organs and finally the diversification of animals. Because taxon sampling is essential to understand evolution we implement these technologies into previously not investigated but highly informative species. Furthermore, we use the sequencing information to resolve important evolutionary relationships in the animal tree of life. Albeit 20 years of successful research has led to the higher resolution in animal relationships, several nodes have not yet been resolved. I use comparative genomics, e.g. to identify syntenies and rare genomic changes to contribute to solve the last mysteries of the placement of several animal taxa (position of Ctenophora, and Xenacoelomorpha, internal branching of Trochozoa).

  • Show author(s) (2023). The localization of Toll and Imd pathway and complement system components and their response to Vibrio infection in the nemertean Lineus ruber. BMC Biology.
  • Show author(s) (2023). Peripheral and central employment of acid-sensing ion channels during early bilaterian evolution. eLIFE. 25 pages.
  • Show author(s) (2023). Annelid functional genomics reveal the origins of bilaterian life cycles. Nature. 105-110.
  • Show author(s) (2022). Marine animal evolutionary developmental biology—Advances through technology development. Evolutionary Applications. 580-588.
  • Show author(s) (2022). Brachiopod and mollusc biomineralisation is a conserved process that was lost in the phoronid–bryozoan stem lineage. EVODEVO. 1-11.
  • Show author(s) (2021). The evolution of the metazoan Toll receptor family and its expression during protostome development. BMC Ecology and Evolution.
  • Show author(s) (2021). Publisher Correction: Conservative route to genome compaction in a miniature annelid (Nature Ecology & Evolution, (2021), 5, 2, (231-242), 10.1038/s41559-020-01327-6). Nature Ecology and Evolution. 262.
  • Show author(s) (2021). Nemertean, Brachiopod, and Phoronid Neuropeptidomics Reveals Ancestral Spiralian Signaling Systems. Molecular Biology and Evolution (MBE). 4847-4866.
  • Show author(s) (2021). Molecular evidence for a single origin of ultrafiltration-based excretory organs. Current Biology. 3629-3638.
  • Show author(s) (2021). Molecular and morphological analysis of the developing nemertean brain indicates convergent evolution of complex brains in Spiralia. BMC Biology.
  • Show author(s) (2021). FGF signaling acts on different levels of mesoderm development within Spiralia. Development.
  • Show author(s) (2020). Kompleksitetens svøpe - om "tidlige" og "seine" greiner på livets tre. Naturen. 97-104.
  • Show author(s) (2020). Hox gene expression during development of the phoronid Phoronopsis harmeri. EVODEVO.
  • Show author(s) (2020). Conservative route to genome compaction in a miniature annelid. Nature Ecology and Evolution. 231-242.
  • Show author(s) (2019). Morphology of the nervous system of monogonont rotifer Epiphanes senta with a focus on sexual dimorphism between feeding females and dwarf males. Frontiers in Zoology. 1-13.
  • Show author(s) (2019). Molecular patterning during the development of Phoronopsis harmeri reveals similarities to rhynchonelliform brachiopods. EVODEVO.
  • Show author(s) (2019). Hox gene expression in postmetamorphic juveniles of the brachiopod Terebratalia transversa. EVODEVO.
  • Show author(s) (2019). Evolutionary Implications of the microRNA- and piRNA Complement of Lepidodermella squamata (Gastrotricha). Non-coding RNA. 17 pages.
  • Show author(s) (2019). En vitenskap for fremtiden.
  • Show author(s) (2019). Embryonic expression of priapulid Wnt genes. Development, Genes and Evolution. 125-135.
  • Show author(s) (2019). Convergent evolution of a vertebrate-like methylome in a marine sponge. Nature Ecology and Evolution. 1464-1473.
  • Show author(s) (2019). Active mode of excretion across digestive tissues predates the origin of excretory organs. PLoS Biology. 1-22.
  • Show author(s) (2019). A nemertean excitatory peptide/CCHamide regulates ciliary swimming in the larvae of Lineus longissimus. Frontiers in Zoology. 1-14.
  • Show author(s) (2019). A developmental perspective on the evolution of the nervous system. Developmental Biology. 1-12.
  • Show author(s) (2018). Xenacoelomorph neuropeptidomes reveal a major expansion of neuropeptide systems during early bilaterian evolution. Molecular Biology and Evolution (MBE). 2528-2543.
  • Show author(s) (2018). Plan S: -Håper Nature legger om.
  • Show author(s) (2018). Pairwise comparisons across species are problematic when analyzing functional genomic data. Proceedings of the National Academy of Sciences of the United States of America. E409-E417.
  • Show author(s) (2018). Early metazoan cell type diversity and the evolution of multicellular gene regulation. Nature Ecology and Evolution. 1176-1188.
  • Show author(s) (2018). Convergent evolution of bilaterian nerve cords. Nature. 45-50.
  • Show author(s) (2018). A safer, urea-based in situ hybridization method improves detection of gene expression in diverse animal species. Developmental Biology. 15-23.
  • Show author(s) (2017). Increased taxon sampling reveals thousands of hidden orthologs in flatworms. Genome Research. 1263-1272.
  • Show author(s) (2017). Evolutionary and behavioral analysis of neuropeptides in bilaterians .
  • Show author(s) (2017). Clustered brachiopod Hox genes are not expressed collinearly and are associated with lophotrochozoan novelties. Proceedings of the National Academy of Sciences of the United States of America. E1913-E1922.
  • Show author(s) (2017). Cleavage modification did not alter blastomere fates during bryozoan evolution. BMC Biology.
  • Show author(s) (2017). An ancient FMRFamide-related peptide-receptor pair induces defence behaviour in a brachiopod larva. Open Biology.
  • Show author(s) (2016). Xenacoelomorpha's significance for understanding bilaterian evolution. Current Opinion in Genetics and Development. 48-54.
  • Show author(s) (2016). Xenacoelomorpha is the sister group to Nephrozoa. Nature. 89-93.
  • Show author(s) (2016). The larval nervous system of the penis worm Priapulus caudatus (Ecdysozoa). Philosophical Transactions of the Royal Society of London. Biological Sciences. 10 pages.
  • Show author(s) (2016). Molecular regionalization in the compact brain of the meiofaunal annelid Dinophilus gyrociliatus (Dinophilidae). EVODEVO. 1-21.
  • Show author(s) (2016). Embryonic chirality and the evolution of spiralian left - Right asymmetries. Philosophical Transactions of the Royal Society of London. Biological Sciences. 10 pages.

More information in national current research information system (CRIStin)

Developmental Diversity And The Evolution of Animal Organ Systems

Horizon 2020 Grants:


Research Council Norway (NFR)

  • Norwegian Research Grant: FRIPRO Grant "EVOBRAIN" (The origin and evolution of bilaterian brains) (2019-2023), Project Number 288541

  • Collaborative Project 2021: "A Norwegian BioGenome initiative: the initial Launch phase" (Project Number 326819)

Andreas Hejnol is Professor and research group leader of “Comparative Developmental Biology” at the Department of Biological Sciences (BIO) in Bergen, Norway. After obtaining his Ph.D. in Comparative Zoology from the Free University Berlin, Germany in 2002 he worked as a postdoctoral fellow in the laboratory of Ralf Schnabel in Braunschweig and at the Kewalo Marine Laboratory in the lab of Mark Q. Martindale in Hawaii. He led a research group at the Sars Centre from 2009-2019. His current research interest on descriptive, experimental molecular developmental biology of a broad range of invertebrates and includes comparative genomic approaches and phylogenomics. The main research goal is to understand the evolutionary origin and diversification of animal body plans, cell types and organ systems. He is ERC Consolidator Grant holder and received for his achievements in Evolutionary Developmental Biology and Comparative Zoology the prestigious Alexander O. Kovalevsky Medal from the St. Petersburg Society for Naturalists in 2018. Since 2021 he is also Professor for Zoology and Director of the Institute for Zoology and Evolutionary Research and the Phyletic Museum of the Friedrich Schiller University Jena, Germany.