In this article, we will thoroughly explore the topic of Evx1, a topic that has captured the attention of people of all ages and walks of life. From its importance in history to its relevance today, Evx1 has been the subject of study and interest for researchers, academics and enthusiasts alike. Through a comprehensive analysis, we will examine the various aspects related to Evx1, from its origins to its impact on modern society. With the intention of providing a complete and detailed overview of Evx1, this article will delve into its many facets, offering a broad and enriching perspective to understand its true meaning and scope.
Evx1 is a mammalian gene located downstream of the HoxA cluster, which encodes for a homeobox transcription factor. Evx1 is a homolog of even-skipped (eve), which is a pair-rule gene that regulates body segmentation in Drosophila.[1][2] The expression of Evx1 is developmentally regulated, displaying a biphasic expression pattern with peak expression in the primitive streak during gastrulation and in interneurons during neural development.[3][4] Evx1 has been shown to regulate anterior-posterior patterning during gastrulation by acting as a downstream effector of the Wnt and BMP signalling pathways.[4][5] It is also a critical regulator of interneuron identity.[6]
Despite a regulatory role in both of these processes, the Evx1 KO mouse is viable and displays no overt phenotype after birth.[4][6]
A divergent long non-coding RNA (Evx1as) is also expressed from the locus, which is temporally and spatially co-expressed with Evx1.[3][4][7] Evx1as does not have a function beyond that of Evx1 (in trans);[4] however, it has been shown to regulate Evx1 at the locus (in cis).[7]