Transposable element derived DNaseI-hypersensitive sites in the human genome
2006

Transposable Elements and Gene Regulation in Humans

Sample size: 14216 publication 10 minutes Evidence: moderate

Author Information

Author(s): Mariño-Ramírez Leonardo, Jordan I King

Primary Institution: National Center for Biotechnology Information, National Institutes of Health

Hypothesis

Transposable elements contribute to the evolution of gene regulatory sequences in the human genome.

Conclusion

Transposable elements provide a mechanism for generating functionally relevant gene regulatory divergence between evolutionary lineages.

Supporting Evidence

  • 23% of DNaseI-hypersensitive sites contain transposable element-derived sequences.
  • TE-derived HS sites are functionally relevant in driving gene expression in CD4+ T cells.
  • Genes with TE-derived HS sites are statistically over-represented in immune response functions.

Takeaway

Some parts of our DNA come from jumping genes called transposable elements, which help control how our genes work, especially in immune cells.

Methodology

The study used high throughput mapping of DNaseI-hypersensitive sites in CD4+ T cells to evaluate the contribution of transposable elements to gene regulatory sequences.

Potential Biases

Potential bias in the interpretation of the functional relevance of TE-derived HS sites due to their lack of evolutionary conservation.

Limitations

The study primarily focused on HS sites in CD4+ T cells and may not generalize to other cell types.

Participant Demographics

The study analyzed HS sites specifically in human CD4+ T cells.

Statistical Information

P-Value

0

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1745-6150-1-20

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