UTX (gene) explained

Lysine-specific demethylase 6A also known as Ubiquitously transcribed tetratricopeptide repeat, X chromosome (UTX), is a protein which in humans is encoded by the KDM6A gene.[1] [2] [3] It belongs to the 2-oxoglutarate (2OG)-dependent dioxygenase superfamily.

Function

UTX has been linked with demethylation of lysine residues on histone, in particular H3K27, resulting in a gene de-repression, a potential means of regulating cellular metabolism.[4]

Further reading

Notes and References

  1. Web site: Entrez Gene: KDM6A lysine demethylase 6A .
  2. Lahn BT, Page DC . Functional coherence of the human Y chromosome . Science . 278 . 5338 . 675–80 . October 1997 . 9381176 . 10.1126/science.278.5338.675 . 1997Sci...278..675L .
  3. Greenfield A, Carrel L, Pennisi D, Philippe C, Quaderi N, Siggers P, Steiner K, Tam PP, Monaco AP, Willard HF, Koopman P . The UTX gene escapes X inactivation in mice and humans . Hum. Mol. Genet. . 7 . 4 . 737–42 . April 1998 . 9499428 . 10.1093/hmg/7.4.737 . free .
  4. Lee MG, Villa R, Trojer P, Norman J, Yan KP, Reinberg D, Di Croce L, Shiekhattar R . Demethylation of H3K27 regulates polycomb recruitment and H2A ubiquitination . Science . 318 . 5849 . 447–50 . October 2007 . 17761849 . 10.1126/science.1149042 . 2007Sci...318..447L . 23883131 . free .