| Literature DB >> 28515211 |
Fatwa Adikusuma1,2,3, Daniel Pederick1,2, Dale McAninch1,2, James Hughes1,2, Paul Thomas4,2,5.
Abstract
Gene duplication provides spare genetic material that evolution can craft into new functions. Sox2 and Sox3 are evolutionarily related genes with overlapping and unique sites of expression during embryogenesis. It is currently unclear whether SOX2 and SOX3 have identical or different functions. Here, we use CRISPR/Cas9-assisted mutagenesis to perform a gene-swap, replacing the Sox3 ORF with the Sox2 ORF to investigate their functional equivalence in the brain and testes. We show that increased expression of SOX2 can functionally replace SOX3 in the development of the infundibular recess/ventral diencephalon, and largely rescues pituitary gland defects that occur in Sox3 null mice. We also show that ectopic expression of SOX2 in the testes functionally rescues the spermatogenic defect of Sox3 null mice, and restores gene expression to near normal levels. Together, these in vivo data provide strong evidence that SOX2 and SOX3 proteins are functionally equivalent.Entities:
Keywords: CRISPR/CAS9 mutagenesis; SOXB1 genes; gene swap
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Year: 2017 PMID: 28515211 PMCID: PMC5500146 DOI: 10.1534/genetics.117.202549
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562