Microphthalmia and Disrupted Retinal Development Due to a LacZ Knock-in/Knock-Out Allele at the Vsx2 Locus

Francesca R Napoli,1 Xiaodong Li,1 Alan A Hurtado,2 Edward M Levine1,3 1Department of Ophthalmology and Visual Sciences, Vanderbilt University Medical Center, Nashville, TN, 37232, USA; 2Program in Chemical and Physical Biology, Vanderbilt University, Nashville, TN, 37232, USA; 3Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, 37232, USACorrespondence: Edward M Levine, Email [email protected]: Visual System Homeobox 2 (Vsx2) is a transcription factor expressed in the developing retina that regulates tissue identity, growth, and fate determination. Several mutations in the Vsx2 gene exist in mice, including a spontaneous nonsense mutation and two targeted missense mutations originally identified in humans. Here, we expand the genetic repertoire to include a LacZ reporter allele (Vsx2LacZ) designed to express beta-Galactosidase (bGal) and simultaneously disrupt Vsx2 function (knock-in/knock-out).Methods: We generated a Vsx2LacZ reporter allele with an in-frame fusion to the Vsx2 coding sequence immediately following exon 2. Germline transmission was assessed with genomic DNA PCR and Western blot analysis was used to describe VSX2 expression from the mutant allele (LacZ). Eye size quantification and immunohistology were used to describe the embryonic and postnatal retinal phenotypes of LacZ homozygous and heterozygous mice. The contribution of Mitf to LacZ mutant microphthalmia was probed with the semi-dominant negative Mitfmi allele.Results: The retinal expression pattern of bGal is concordant with VSX2, and the mutant allele is recessive. Vsx2LacZ homozygous mice have congenital bilateral microphthalmia accompanied by defects in retinal development including ectopic expression of non-retinal genes, reduced proliferation, delayed neurogenesis, aberrant tissue morphology, and an absence of bipolar interneurons - all hallmarks of Vsx2 loss-of-function. The Mitfmi allele reduced the severity of microphthalmia caused by the Vsx2LacZ allele. Unexpectedly, the mutant VSX2 protein is stably expressed, and there are subtle differences in eye size and early retinal neurogenesis when compared to the null mutant, ocular retardation J.Conclusion: The perdurance of the mutant VSX2 protein combined with subtle deviations from the null phenotype leaves open the possibility that Vsx2LacZ allele is not a complete knock-out. The Vsx2LacZ allele exhibits loss-of-function characteristics and adds to the genetic toolkit for understanding Vsx2 function.Keywords: LacZ, reporter knock-in, Vsx2, Chx10, retina, proliferation, lineage fidelity, neurogenesis, immunohistology