Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships

• Published in: Genes Vol. 14; no. 1; p. 222
• Main Authors: Underwood, Adam, Rasicci, Daniel T, Hinds, David, Mitchell, Jackson T, Zieba, Jacob K, Mills, Joshua, Arnold, Nicholas E, Cook, Taylor W, Moustaqil, Mehdi, Gambin, Yann, Sierecki, Emma, Fontaine, Frank, Vanderweele, Sophie, Das, Akansha S, Cvammen, William, Sirpilla, Olivia, Soehnlen, Xavier, Bricker, Kristen, Alokaili, Maram, Green, Morgan, Heeringa, Sadie, Wilstermann, Amy M, Freeland, Thomas M, Qutob, Dinah, Milsted, Amy, Jauch, Ralf, Triche, Jr, Timothy J, Krawczyk, Connie M, Bupp, Caleb P, Rajasekaran, Surender, Francois, Mathias, Prokop, Jeremy W
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 14.01.2023; MDPI
• Subjects: Amino Acid Sequence; Amino acids; Blood-brain barrier; Cancer; Dimerization; Disease; Dysplasia; Genes; Genomes; Genotype; Genotypes; High mobility group proteins; High Mobility Group Proteins - chemistry; High Mobility Group Proteins - genetics; High Mobility Group Proteins - metabolism; Humans; Intellectual disabilities; Mutation; Neurological complications; Phenotypes; Proteins; Seizures; SOX Transcription Factors - genetics; Sox9 protein; SOXB2 Transcription Factors - genetics; SOXB2 Transcription Factors - metabolism; SOXE Transcription Factors - genetics; SOXF Transcription Factors - genetics; SOXF Transcription Factors - metabolism; transcription factor; paralog mapping; SOX genes; developmental biology; variant data integration
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes14010222

The SOX transcription factor family is pivotal in controlling aspects of development. To identify genotype-phenotype relationships of SOX proteins, we performed a non-biased study of SOX using 1890 open-reading frame and 6667 amino acid sequences in combination with structural dynamics to interpret 3999 gnomAD, 485 ClinVar, 1174 Geno2MP, and 4313 COSMIC human variants. We identified, within the HMG (High Mobility Group)- box, twenty-seven amino acids with changes in multiple SOX proteins annotated to clinical pathologies. These sites were screened through Geno2MP medical phenotypes, revealing novel SOX15 R104G associated with musculature abnormality and SOX8 R159G with intellectual disability. Within gnomAD, SOX18 E137K (rs201931544), found within the HMG box of ~0.8% of Latinx individuals, is associated with seizures and neurological complications, potentially through blood-brain barrier alterations. A total of 56 highly conserved variants were found at sites outside the HMG-box, including several within the SOX2 HMG-box-flanking region with neurological associations, several in the SOX9 dimerization region associated with Campomelic Dysplasia, SOX14 K88R (rs199932938) flanking the HMG box associated with cardiovascular complications within European populations, and SOX7 A379V (rs143587868) within an SOXF conserved far C-terminal domain heterozygous in 0.716% of African individuals with associated eye phenotypes. This SOX data compilation builds a robust genotype-to-phenotype association for a gene family through more robust ortholog data integration.