SOX gene family

SOXB subfamily, C-terminal next to HMG box
Identifiers
SymbolSOXp
PfamPF12336
InterProIPR022097
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
SOXE, N-terminal
Identifiers
SymbolSox_N
PfamPF12444
InterProIPR022151
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
SOXF, C-terminal, 9aaTAD
Identifiers
SymbolSOX_C
InterProIPR021934
PROSITEPS51516
SOXF, central
Identifiers
SymbolSox17_18_mid
PfamPF12067
InterProIPR033392
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

SOX genes (SRY-related HMG-box 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 (for high mobility group). 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.

Sox genes are defined as containing the HMG box of a gene involved in sex determination called SRY, which resides on the Y-chromosome. There are 20 SOX genes present in humans and mice, and 8 present in Drosophila. Almost all Sox genes show at least 50% amino acid similarity with the HMG box in Sry. The family is divided into subgroups according to homology within the HMG domain and other structural motifs, as well as according to functional assays.[1]

The developmentally important Sox family has no singular function, and many members possess the ability to regulate several different aspects of development. While many Sox genes are involved in sex determination, some are also important in processes such as neuronal development. For example, Sox2 and Sox3 are involved in the transition of epithelial granule cells in the cerebellum to their migratory state. Sox 2 is also a transcription factor in the maintenance of pluripotency in both Early Embryos and ES Cells.[2] Granule cells then differentiate to granule neurons, with Sox11 being involved in this process.[3] It is thought that some Sox genes may be useful in the early diagnosis of childhood brain tumours due to this sequential expression in the cerebellum, making them a target for significant research.

Sox proteins bind to the sequence WWCAAW and similar sequences (W=A or T). They have weak binding specificity and unusually low affinity for DNA. Sox genes are related to the Tcf/Lef1 group of genes which also contain a sequence-specific high mobility group and have a similar sequence specificity (roughly TWWCAAAG).[4]

  1. ^ Bowles, J; Schepers G; Koopman P. (November 2000). "Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators". Dev. Biol. 227 (2): 239–55. doi:10.1006/dbio.2000.9883. PMID 11071752.
  2. ^ Takahashi, Kazutoshi; Yamanaka, Shinya (2006-08-25). "Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors". Cell. 126 (4): 663–676. doi:10.1016/j.cell.2006.07.024. hdl:2433/159777. ISSN 0092-8674. PMID 16904174.
  3. ^ Rex, M; Church, R; Tointon, K; Ichihashi, RM; Mokhtar, S; Uwanogho, D; Sharpe, PT; Scotting, PJ (March 1998). "Granule cell development in the cerebellum is punctuated by changes in Sox gene expression". Molecular Brain Research. 55 (1): 28–34. doi:10.1016/S0169-328X(97)00354-9. PMID 9645957.
  4. ^ Lefebvre V, Dumitriu B, Penzo-Méndez A, Han Y, Pallavi B (2007). "Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors". Int. J. Biochem. Cell Biol. 39 (12): 2195–214. doi:10.1016/j.biocel.2007.05.019. PMC 2080623. PMID 17625949.