SoxC group is group C of Sry-related HMG box proteins transcription factors. SoxC genes play an important role in determining the cell fate of neuronal mesenchymal progenitor cells in many developmental processes. [1]
In Drosophila melanogaster (fly), Caenorhabditis elegans (worm), and other lower animals SoxC is made up of only one member, but humans, mice and most other vertebrates have three members of the SoxC group. [2] The three are Sox4, Sox11, and Sox12. These three are extremely similar to one another, more so than other proteins, but they are all highly distinct in the way that they bind DNA and active transcription in vitro with different affinity. [3] The three found in humans and other vertebrates are single-exon genes. [2] The SoxC proteins have 2 domains, the first an Sry-related HMG box DNA binding domain that is located near the N-terminal and the second a trans-activation domain, known as TAD, located near the C-terminal. [3] Although these are transcription factors, to this date there is no evidence of post-translational modifications on SoxC members, but they can work cooperatively with other proteins though, such as transcription factors Brn2 and Brn1. [3]
All of the SoxC proteins share 67% identity and 94% similarity in the 33 residues of the C-terminal domain. [3] All SoxC genes show 84% identity and 95% similarity to one another in the HMG box, which is just slightly more highly conserved than the C-terminal domain. [3] The SoxC proteins only have between 45% and 67% identity to Sry and the other Sox proteins. [3] The SoxC genes found in the Drosophila melanogaster (fly), Caenorhabditis elegans (worm), and other lower animals are closely linked to those found in humans and other vertebrates. [3] The SoxC genes are highly conserved through vertebrate evolution and are similar enough to those in invertebrates and other lower animal species to speculate that these are based on an evolutionary necessity from before vertebrates and invertebrates separated through evolution. [3]
If these SoxC proteins were missing during developmental stages it would cause widespread problems through the body of mice, and in many cases death. [3] These have not been studied in humans though, because no occurrences have been linked to congential malformations of any of these proteins. [2] In mice however, mice embryos without Sox4 die of heart defects, but mice newborns without Sox11 do live but have widespread defects. [3] Mice without Sox12 are viable and show no outward signs of malformation. [3] Some of the common human malformations are also seen in mice with mutated SoxC, such as cleft palate or heart outflow tract malformation. [3] There is no evidence of the correlation between SoxC mutations in humans and these malformations, but there is speculation.
Sox4 facilitates differentiation of lymphocytes, osteoblasts, pancreatic beta cells and along with Sox11 promotes neural differentiation. In recent years, the belief has raised that SoxC genes may lead to tumor prognosis at elevated levels. [2] Increased expression of Sox11 and Sox4 are seen in numerous tumors and cancers and it is possible that the tumors differ depending on the circumstance and primary transformation mechanism. [2]
Sex-determining region Y protein (SRY), or testis-determining factor (TDF), is a DNA-binding protein encoded by the SRY gene that is responsible for the initiation of male sex determination in therian mammals. SRY is an intronless sex-determining gene on the Y chromosome. mutations in this gene lead to a range of disorders of sex development with varying effects on an individual's phenotype and genotype.
SOX genes encode a family of transcription factors that bind to the minor groove in DNA, and belong to a super-family of genes characterized by a homologous sequence called the HMG-box. This HMG box is a DNA binding domain that is highly conserved throughout eukaryotic species. Homologues have been identified in insects, nematodes, amphibians, reptiles, birds and a range of mammals. However, HMG boxes can be very diverse in nature, with only a few amino acids being conserved between species.
In evolutionary developmental biology, Paired box (Pax) genes are a family of genes coding for tissue specific transcription factors containing an N-terminal paired domain and usually a partial, or in the case of four family members, a complete homeodomain to the C-terminus. An octapeptide as well as a Pro-Ser-Thr-rich C terminus may also be present. Pax proteins are important in early animal development for the specification of specific tissues, as well as during epimorphic limb regeneration in animals capable of such.
Paired box protein Pax-6, also known as aniridia type II protein (AN2) or oculorhombin, is a protein that in humans is encoded by the PAX6 gene.
High-Mobility Group or HMG is a group of chromosomal proteins that are involved in the regulation of DNA-dependent processes such as transcription, replication, recombination, and DNA repair.
Teneurins are a family of phylogenetically conserved single-pass transmembrane glycoproteins expressed during pattern formation and morphogenesis. The name refers to "ten-a" and "neurons", the primary site of teneurin expression. Ten-m refers to tenascin-like protein major.
Transcription factor SOX-9 is a protein that in humans is encoded by the SOX9 gene.
Transcription factor SOX-4 is a protein that in humans is encoded by the SOX4 gene.
C-terminal-binding protein 2 also known as CtBP2 is a protein that in humans is encoded by the CTBP2 gene.
Transcription factor SOX-3 is a protein that in humans is encoded by the SOX3 gene. This gene encodes a member of the SOX family of transcription factors involved in the regulation of embryonic brain development and in determination of cell fate. The encoded protein acts as a transcriptional activator.
Transcription factor SOX-6 is a protein that in humans is encoded by the SOX6 gene.
Transcription factor SOX-18 is a protein that in humans is encoded by the SOX18 gene.
Transcription factor SOX-8 is a protein that in humans is encoded by the SOX8 gene.
SOX12 is a protein that in humans is encoded by the SOX12 gene. Sox12 belongs to the SoxC group of Sox family of transcription factors, together with Sox4 and Sox11. Sox12-null knockout mice appear normal, unlike Sox4 or Sox11 knockout mice. This probably comes from functional redundancy with Sox4 and Sox11. Sox12 is a weaker activator than both Sox4 and Sox11 in mouse.
SOX1 is a gene that encodes a transcription factor with a HMG-box DNA-binding domain and functions primarily in neurogenesis. SOX1, SOX2 and SOX3, members of the SOX gene family, contain transcription factors related to SRY, the testis-determining factor.
Notch proteins are a family of type-1 transmembrane proteins that form a core component of the Notch signaling pathway, which is highly conserved in metazoans. The Notch extracellular domain mediates interactions with DSL family ligands, allowing it to participate in juxtacrine signaling. The Notch intracellular domain acts as a transcriptional activator when in complex with CSL family transcription factors. Members of this Type 1 transmembrane protein family share several core structures, including an extracellular domain consisting of multiple epidermal growth factor (EGF)-like repeats and an intracellular domain transcriptional activation domain (TAD). Notch family members operate in a variety of different tissues and play a role in a variety of developmental processes by controlling cell fate decisions. Much of what is known about Notch function comes from studies done in Caenorhabditis elegans (C.elegans) and Drosophila melanogaster. Human homologs have also been identified, but details of Notch function and interactions with its ligands are not well known in this context.
Vasa is an RNA binding protein with an ATP-dependent RNA helicase that is a member of the DEAD box family of proteins. The vasa gene is essential for germ cell development and was first identified in Drosophila melanogaster, but has since been found to be conserved in a variety of vertebrates and invertebrates including humans. The Vasa protein is found primarily in germ cells in embryos and adults, where it is involved in germ cell determination and function, as well as in multipotent stem cells, where its exact function is unknown.
In molecular biology the DM domain is a protein domain first discovered in the doublesex proteins of Drosophila melanogaster and is also seen in C. elegans and mammalian proteins. In D. melanogaster the doublesex gene controls somatic sexual differentiation by producing alternatively spliced mRNAs encoding related sex-specific polypeptides. These proteins are believed to function as transcription factors on downstream sex-determination genes, especially on neuroblast differentiation and yolk protein genes transcription.
SRY -box 30 is a protein that in humans is encoded by the SOX30 gene.
SRY-box 7 is a protein that in humans is encoded by the SOX7 gene.