Barrier to autointegration factor 1 explained

Barrier-to-autointegration factor is a protein that in humans is encoded by the BANF1 gene.[1] [2] It is a member of the barrier-to-autointegration factor family of proteins.

Function

The protein encoded by this gene was identified by its ability to protect retroviruses from intramolecular integration and therefore promote intermolecular integration into the host cell genome. The endogenous function of the protein is unknown. The protein forms a homodimer which localizes to the nucleus and is specifically associated with chromosomes during mitosis. This protein binds to DNA in a non-specific manner and studies in rodents suggest that it also binds to lamina-associated polypeptide 2, a component of the nuclear lamina. It also associates with the LEM Domain containing proteins LAP2, Emerin, and MAN1. The protein's DNA binding ability is modulated by ATP concentration.[3]

Interactions

Barrier to autointegration factor 1 has been shown to interact with Thymopoietin.[4]

Clinical relevance

Mutations in this gene have been shown to cause hereditary progeroid syndrome.[5]

See also

Further reading

Notes and References

  1. Lee MS, Craigie R . A previously unidentified host protein protects retroviral DNA from autointegration . Proc Natl Acad Sci U S A . 95 . 4 . 1528–33 . Mar 1998 . 9465049 . 19075 . 10.1073/pnas.95.4.1528 . 1998PNAS...95.1528L . free .
  2. Web site: Entrez Gene: BANF1 barrier to autointegration factor 1.
  3. Sridharan S, Kurzawa N, Werner T, Günthner I, Helm D, Huber W, Bantscheff M, Savitski MM . Proteome-wide solubility and thermal stability profiling reveals distinct regulatory roles for ATP . Nature Communications . 10 . 1 . 1155 . March 2019 . 30858367 . 10.1038/s41467-019-09107-y . 6411743 . 2019NatCo..10.1155S .
  4. Furukawa K . LAP2 binding protein 1 (L2BP1/BAF) is a candidate mediator of LAP2-chromatin interaction . J. Cell Sci. . 112 . Pt 15. 2485–92 . August 1999 . 10.1242/jcs.112.15.2485 . 10393804 .
  5. Puente XS, Quesada V, Osorio FG, Cabanillas R, Cadiñanos J, Fraile JM, Ordóñez GR, Puente DA, Gutiérrez-Fernández A, Fanjul-Fernández M, Lévy N, Freije JM, López-Otín C . Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome . Am. J. Hum. Genet. . 88 . 5 . 650–6 . May 2011 . 21549337 . 3146734 . 10.1016/j.ajhg.2011.04.010 .