| Literature DB >> 33922911 |
Antonella Riva1,2, Antonella Gambadauro3, Valeria Dipasquale3, Celeste Casto3, Maria Domenica Ceravolo3, Andrea Accogli1,4, Marcello Scala2,5, Giorgia Ceravolo3, Michele Iacomino1, Federico Zara1,2, Pasquale Striano2,5, Caterina Cuppari3, Gabriella Di Rosa6, Maria Concetta Cutrupi3, Vincenzo Salpietro2,5, Roberto Chimenz7.
Abstract
Microphthalmia, anophthalmia, and coloboma (MAC) are a group of congenital eye anomalies that can affect one or both eyes. Patients can present one or a combination of these ocular abnormalities in the so called "MAC spectrum". The KIF17 gene encodes the kinesin-like protein Kif17, a microtubule-based, ATP-dependent, motor protein that is pivotal for outer segment development and disc morphogenesis in different animal models, including mice and zebrafish. In this report, we describe a Sicilian family with two siblings affected with congenital coloboma, microphthalmia, and a mild delay of motor developmental milestones. Genomic DNA from the siblings and their unaffected parents was sequenced with a clinical exome that revealed compound heterozygous variants in the KIF17 gene (NM_020816.4: c.1255C > T (p.Arg419Trp); c.2554C > T (p.Arg852Cys)) segregating with the MAC spectrum phenotype of the two affected siblings. Variants were inherited from the healthy mother and father, are present at a very low-frequency in genomic population databases, and are predicted to be deleterious in silico. Our report indicates the potential co-segregation of these biallelic KIF17 variants with microphthalmia and coloboma, highlighting a potential conserved role of this gene in eye development across different species.Entities:
Keywords: KIF17; MAC spectrum; coloboma; congenital eye defects; microphthalmia
Year: 2021 PMID: 33922911 DOI: 10.3390/ijms22094471
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923