4.4 Article

Assessing the regulatory potential of transposable elements using chromatin accessibility profiles of maize transposons

Journal

GENETICS
Volume 217, Issue 1, Pages -

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1093/genetics/iyaa003

Keywords

transposable elements; cis-regulatory regions; ATAC-seq; DNA methylation; Zea mays

Funding

  1. NSF [IOS-1934384, IOS-1856627, IOS-1844427, IOS1546727]
  2. Minnesota Agricultural Experiment Station [MIN 71-068]
  3. Pew Charitable Trusts
  4. NSF PRFB [IOS-1905869]

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Transposable elements (TEs) can create regulatory variation in maize genomes by disrupting existing DNA regulatory elements and creating novel ones, potentially leading to changes in gene expression. The presence of TEs interspersed with genes in maize genomes offers opportunities for significant allelic variation. Some TEs carrying accessible chromatin regions (ACRs) have been found to be associated with higher expression of nearby genes, suggesting a role in providing novel regulatory elements. These findings highlight the potential for a subset of TEs to rewire transcriptional responses in eukaryotic genomes.
Transposable elements (TEs) have the potential to create regulatory variation both through the disruption of existing DNA regulatory elements and through the creation of novel DNA regulatory elements. In a species with a large genome, such as maize, many TEs interspersed with genes create opportunities for significant allelic variation due to TE presence/absence polymorphisms among individuals. We used information on putative regulatory elements in combination with knowledge about TE polymorphisms in maize to identify TE insertions that interrupt existing accessible chromatin regions (ACRs) in B73 as well as examples of polymorphic TEs that contain ACRs among four inbred lines of maize including B73, Mo17, W22, and PH207. The TE insertions in three other assembled maize genomes (Mo17, W22, or PH207) that interrupt ACRs that are present in the B73 genome can trigger changes to the chromatin, suggesting the potential for both genetic and epigenetic influences of these insertions. Nearly 20% of the ACRs located over 2 kb from the nearest gene are located within an annotated TE. These are regions of unmethylated DNA that show evidence for functional importance similar to ACRs that are not present within TEs. Using a large panel of maize genotypes, we tested if there is an association between the presence of TE insertions that interrupt, or carry, an ACR and the expression of nearby genes. While most TE polymorphisms are not associated with expression for nearby genes, the TEs that carry ACRs exhibit enrichment for being associated with higher expression of nearby genes, suggesting that these TEs may contribute novel regulatory elements. These analyses highlight the potential for a subset of TEs to rewire transcriptional responses in eukaryotic genomes.

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