Hox gene

Hox genes, a subset of homeobox genes, are a group of related genes that specify regions of the body plan of an embryo along the head-tail axis of animals. Hox proteins encode and specify the characteristics of 'position', ensuring that the correct structures form in the correct places of the body. For example, Hox genes in insects specify which appendages form on a segment (for example, legs, antennae, and wings in fruit flies), and Hox genes in vertebrates specify the types and shape of vertebrae that will form. In segmented animals, Hox proteins thus confer segmental or positional identity, but do not form the actual segments themselves.

Studies on Hox genes in ciliated larvae have shown they are only expressed in future adult tissues. In larvae with gradual metamorphosis the Hox genes are activated in tissues of the larval body, generally in the trunk region, that will be maintained through metamorphosis. In larvae with complete metamorphosis the Hox genes are mainly expressed in juvenile rudiments and are absent in the transient larval tissues. The larvae of the hemichordate species Schizocardium californicum and the pilidium larva of Nemertea do not express Hox genes.[1][2]

An analogy for the Hox genes can be made to the role of a play director who calls which scene the actors should carry out next. If the play director calls the scenes in the wrong order, the overall play will be presented in the wrong order. Similarly, mutations in the Hox genes can result in body parts and limbs in the wrong place along the body. Like a play director, the Hox genes do not act in the play or participate in limb formation themselves.

The protein product of each Hox gene is a transcription factor. Each Hox gene contains a well-conserved DNA sequence known as the homeobox, of which the term "Hox" was originally a contraction. However, in current usage the term Hox is no longer equivalent to homeobox, because Hox genes are not the only genes to possess a homeobox sequence; for instance, humans have over 200 homeobox genes, of which 39 are Hox genes.[3][4] Hox genes are thus a subset of the homeobox transcription factor genes. In many animals, the organization of the Hox genes in the chromosome is the same as the order of their expression along the anterior-posterior axis of the developing animal, and are thus said to display colinearity.[5][6] Production of Hox gene products at wrong location in the body is associated with metaplasia and predisposes to oncological disease, e.g. Barrett's esophagus is the result of altered Hox coding and is a precursor to esophageal cancer.[7]

  1. ^ Hejnol A, Vellutini BC (January 2017). "Larval Evolution: I'll Tail You Later…". Current Biology. 27 (1): R21–R24. Bibcode:2017CBio...27..R21H. doi:10.1016/j.cub.2016.10.057. PMID 28073016.
  2. ^ Gąsiorowski L, Hejnol A (10 February 2020). "Hox gene expression during development of the phoronid Phoronopsis harmeri". EvoDevo. 11 (2): 2. doi:10.1186/s13227-020-0148-z. PMC 7011278. PMID 32064072.
  3. ^ Holland PW, Booth HA, Bruford EA (October 2007). "Classification and nomenclature of all human homeobox genes". BMC Biology. 5: 47. doi:10.1186/1741-7007-5-47. PMC 2211742. PMID 17963489.
  4. ^ Bürglin TR, Affolter M (June 2016). "Homeodomain proteins: an update". Chromosoma. 125 (3): 497–521. doi:10.1007/s00412-015-0543-8. PMC 4901127. PMID 26464018.
  5. ^ Cite error: The named reference Nature Reviews 2005 was invoked but never defined (see the help page).
  6. ^ Carroll SB (August 1995). "Homeotic genes and the evolution of arthropods and chordates". Nature. 376 (6540): 479–485. Bibcode:1995Natur.376..479C. doi:10.1038/376479a0. PMID 7637779. S2CID 4230019.
  7. ^ Janmaat VT, Nesteruk K, Spaander MC, Verhaar AP, Yu B, Silva RA, et al. (June 2021). "HOXA13 in etiology and oncogenic potential of Barrett's esophagus". Nature Communications. 12 (1): 3354. Bibcode:2021NatCo..12.3354J. doi:10.1038/s41467-021-23641-8. PMC 8184780. PMID 34099670.

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