HOTAIR

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Gene found in humans

title: "HOTAIR" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["antisense-rna", "non-coding-rna"] description: "Gene found in humans" topic_path: "general/antisense-rna" source: "https://en.wikipedia.org/wiki/HOTAIR" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

::summary Gene found in humans ::

HOTAIR (for HOX transcript antisense RNA) is a human gene located between HOXC11 and HOXC12 on chromosome 12. It is the first example of an RNA expressed on one chromosome that has been found to influence the transcription of the HOXD cluster posterior genes located on chromosome 2. The sequence and function of HOTAIR are different in humans and mice. Sequence analysis of HOTAIR revealed that it exists in mammals, has poorly conserved sequences and considerably conserved structures, and has evolved faster than nearby HoxC genes. A subsequent study identified HOTAIR has 32 nucleotides long conserved noncoding element (CNE) that has a paralogous copy in HOXD cluster region (located between HOXD11 and HOXD12), suggesting that the HOTAIR conserved sequences predate whole genome duplication events at the root of vertebrate. While the conserved sequence paralogous with HOXD cluster is 32 nucleotide long, the HOTAIR sequence conserved from human to fish is about 200 nucleotide long and is marked by active enhancer features (bidirectional transcription, H3K4me1 and H3K27ac peaks).

Gene and transcribed RNA product

The HOTAIR gene contains 6,232 bp and encodes a 2.2 kb long noncoding RNA molecule, which controls gene expression. Its source DNA is located within a HOXC gene cluster. It is shuttled from chromosome 12 to chromosome 2 by the Suz-Twelve protein.

Function

The 5′ end of HOTAIR interacts with a Polycomb-group protein Polycomb Repressive Complex 2 (PRC2) and as a result regulates chromatin state. It is required for gene-silencing of the HOXD locus by PRC2. PRC2 is dispensable for HOTAIR-mediated transcriptional silencing. The 3′ end of HOTAIR interacts with the histone demethylase LSD1.

It is an important factor in the epigenetic differentiation of skin over the surface of the body. Skin from various anatomical positions is distinct, e.g. the skin of the eyelid differs markedly from that on the sole.

Clinical significance

HOTAIR is highly expressed in metastatic breast cancers. High levels of expression in primary breast tumours are a significant predictor of subsequent metastasis and death. This is partially due to HOTAIR-mediated overexpression of the HER2 oncogene through sequestration of miR-331-3p, which is a negative regulator of HER2 expression. In cells, especially those that over express PRC2, the prevention of HOTAIR expression leads to a reduction in invasive potential of that cell. It is also involved in esophageal squamous cell carcinoma.

References

References

  1. "Genecards entry on HOTAIR".
  2. (May 2011). "Structural and functional differences in the long non-coding RNA hotair in mouse and human". PLOS Genetics.
  3. (April 2011). "The sequence, structure and evolutionary features of HOTAIR in mammals". BMC Evolutionary Biology.
  4. (April 2020). "Ancestrally Duplicated Conserved Noncoding Element Suggests Dual Regulatory Roles of HOTAIR in cis and trans". iScience.
  5. (August 2008). "Genetics: The production line". Nature.
  6. (June 2007). "Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs". Cell.
  7. (August 2010). "Long noncoding RNA as modular scaffold of histone modification complexes". Science.
  8. (April 2017). "PRC2 is dispensable for ''HOTAIR''-mediated transcriptional repression". The EMBO Journal.
  9. (January 2003). "Homeobox genes, fetal wound healing, and skin regional specificity". The Journal of Investigative Dermatology.
  10. (April 2014). "Lnc RNA HOTAIR functions as a competing endogenous RNA to regulate HER2 expression by sponging miR-331-3p in gastric cancer". Molecular Cancer.
  11. (April 2010). "Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis". Nature.
  12. (November 2013). "Upregulation of the long non-coding RNA HOTAIR promotes esophageal squamous cell carcinoma metastasis and poor prognosis". Molecular Carcinogenesis.

::callout[type=info title="Wikipedia Source"] This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page. ::

antisense-rnanon-coding-rna