FB2026_02 , released June 18, 2026
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Citation
Zrimec, J., Börlin, C.S., Buric, F., Muhammad, A.S., Chen, R., Siewers, V., Verendel, V., Nielsen, J., Töpel, M., Zelezniak, A. (2020). Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure.  Nat. Commun. 11(1): 6141.
FlyBase ID
FBrf0247517
Publication Type
Research paper
Abstract
Understanding the genetic regulatory code governing gene expression is an important challenge in molecular biology. However, how individual coding and non-coding regions of the gene regulatory structure interact and contribute to mRNA expression levels remains unclear. Here we apply deep learning on over 20,000 mRNA datasets to examine the genetic regulatory code controlling mRNA abundance in 7 model organisms ranging from bacteria to Human. In all organisms, we can predict mRNA abundance directly from DNA sequence, with up to 82% of the variation of transcript levels encoded in the gene regulatory structure. By searching for DNA regulatory motifs across the gene regulatory structure, we discover that motif interactions could explain the whole dynamic range of mRNA levels. Co-evolution across coding and non-coding regions suggests that it is not single motifs or regions, but the entire gene regulatory structure and specific combination of regulatory elements that define gene expression levels.
PubMed ID
PubMed Central ID
PMC7708451 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference