 | This article relies on a single source. (December 2020) |
Homeobox protein Nkx-2.8 (sometimes also called Nkx-2.9 especially in mice) is a protein that in humans is encoded by the gene NKX2-8. Nkx-2.8 is a transcription factor responsible for the formation of the branchial and visceral motor neuron subtypes of cranial motor nerves in vertebrates. Nkx-2.8 works together with another transcription factor, Nkx 2.2, to direct neural progenitor cells to their cell fate.
Cell lineage analysis of Nkx 2.9 and Nkx 2.2 double knockout (deficient) mouse embryos shows that cranial nerve alterations are a result of changes in neuronal progenitor cell fate. The trigeminal nerve is not affected in the double knockout mouse embryos, indicating that cell fate alteration is limited to the caudal hindbrain; that Nkx 2.9 and Nkx 2.2 proteins do not play a role in branchial or visceral motor neuron development in the portion of the hindbrain superior to neuromere 4.
Disturbance of Nkx 2.9 and Nkx 2.2 in mouse embryos results in the total loss of the spinal accessory and vagal motor nerves, and a partial loss of the glossopharyngeal and facial motor nerves. However, the somatic hypoglossal and abducens motor nerves are not disrupted.
