Diversity, duplication, and genomic organization of homeobox genes in Lepidoptera

  1. Peter W H Holland1,5
  1. 1 University of Oxford;
  2. 2 University of Oxford, UK Centre for Ecology and Hydrology;
  3. 3 Oxford Brookes University;
  4. 4 -
  • * Corresponding author; email: peter.holland{at}zoo.ox.ac.uk
  • Abstract

    Homeobox genes encode transcription factors with essential roles in patterning and cell fate in developing animal embryos. Many homeobox genes, including Hox and NK genes, are arranged in gene clusters, a feature likely related to transcriptional control. Sparse taxon sampling and fragmentary genome assemblies mean that little is known about dynamics of homeobox gene evolution across Lepidoptera, or how changes in homeobox gene number and organization relate to diversity in this large order of insects. Here we analyze an extensive dataset of high-quality genomes to characterize the number and organization of all homeobox genes in 123 species of Lepidoptera from 23 taxonomic families. We find most Lepidoptera have around 100 homeobox loci, including an unusual Hox gene cluster in which the lab gene is repositioned and the ro gene is next to pb. A topologically associating domain spans much of the gene cluster, suggesting deep regulatory conservation of the Hox cluster arrangement in this insect order. Most Lepidoptera have four Shx genes, divergent zen-derived loci, but these loci underwent dramatic duplication in several lineages with some moths having over 165 homeobox loci in the Hox gene cluster; this expansion is associated with local LINE element density. In contrast, the NK gene cluster content is more stable, although there are differences in organization compared to other insects, and major rearrangements within butterflies. Our analysis represents the first description of homeobox gene content across the order Lepidoptera, exemplifying the potential of newly generated genome assemblies for understanding genome and gene family evolution.

    • Received July 12, 2022.
    • Accepted November 29, 2022.

    This manuscript is Open Access.

    This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International license), as described at http://creativecommons.org/licenses/by/4.0/.

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    1. Genome Res. gr.277118.122 Published by Cold Spring Harbor Laboratory Press

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