HOX genes: The Rosetta Stone of the human cells biology
The cell memory program is a biological process that oversees several aspects of the cell life: i) where the new generated cell will be located ii) the fate of a new cell and the cell phenotype; iii) when it will manifest these features; iv) whether and how many cell divisions may perform; v) when will start apoptosis. Three gene families regulate the program: Polycomb family proteins induce a compact configuration of DNA-chromatin (heterochromatin) repressing HOX genes; Tritorax proteins induce an open configuration of DNA-chromatin (euchromatin), activating the HOX network. Finally, the HOX network that ensures the achievement of cell-specific gene programs mainly through the transcriptional control of the genes (Fig. 1). The Class I homeobox genes (HOX in human, Hox in mouse) are a transcription factor family, involved in embryo development containing a sequence of 183 nucleotides (homeobox) encoding a protein alpha helix-domain structure of 61 aminoacids (homeodomain); the homeodomain recognizes and binds a specific nucleotide sequence on DNA.
The HOX gene family is arranged in four chromosomal loci each containing from 9 to 11 genes located on chromosomes: 7p15 HOXA, 17p21 HOXB, 12q13 HOXC and 2q31 HOXD. Besides, HOX can be aligned, based on the sequence similarity of the homeodomain, in 13 vertical paralogous groups following the overlapping of the 39 genes and based on homeodomain primary structure (Fig. 2). The HOX genes are involved in the hematopoietic stem cell differentiation. The HOX clusters, from HOXC4 to HOXC8 and HOXA1 are always involved in the characterization of hematopoietic stem cell phenotype, in the change of immunoglobulin class, in the permutation of the somatic cells and in lymphomagenesis. The HOX network plays a crucial role in the remodeling of blood vessels during adult life. The meaning of HOX genes in the structuring of the heart has been shown for the first time in studies carried out on birds, Drosophila and the heart of amphibians. Subsequently, it has been deeply studied the role of HOX genes in determining of the anteroposterior polarity (A-P) in the vertebrates embryonic cardiac tube. The correct polarity during embryonic development of the cardiac tube in vertebrates, is crucial for the proper morphogenesis of the mature heart. The Hox genes Hoxd3, Hoxa4, and Hoxd4 are upregulated during the early stages of heart development in chicken embryos. Moreover, Hoxd3 is overexpressed in the region designed to the embryonic heart development, before forming of the cardiac tube.
Single mutations in HOXA1 sequence, is crucial in the determination of severe cardiovascular malformations. Mice knock out for Hoxa1, show defects as interrupted aortic arch, aberrant subclavian artery and Tetralogy of Fallot. Hoxa1 play a key role in the arrangement of the great arteries and heart outflow tract. Moreover, at the early stage of embryonic development, Hoxa1 is expressed in the precursors of cardiac neural crest cells (NCCs), present into the heart. Mice knockout for Hoxa3 gene, show cardiac abnormalities and links between circulatory and respiratory systems. The HOXC5, HOXA5 and HOXB5 expression, induce a development of new pharyngeal arches containing a new aortic arch artery with regular flow. HOXC9 is overexpressed, in human smooth muscle cells and the cardiovascular system during embryogenesis.
The cardiovascular development represents the crucial role that HOX network plays in the arrangement of our body and structures. The cluster is able to regulate and control different gene programs, interacting with miRNAs and ncRNAs. Structural alterations: agenesis during embryonal development, adults malformation, neoplastic transformation, deregulation of physiological and metabolic processes are related to HOX gene aberrations. Maybe in the future The HOX network will be considered as “Rosetta stone of human cell biology”.
Medical School “Federico II” of Naples
Department of Neurosciences reproductive and Odontostomatologic Scineces
Class I Homeobox Genes, “The Rosetta Stone of the Cell Biology”, in the Regulation of Cardiovascular Development.
Curr Med Chem. 2016