| Literature DB >> 33961779 |
Norine Voisin1, Rhonda E Schnur2, Sofia Douzgou3, Susan M Hiatt4, Cecilie F Rustad5, Natasha J Brown6, Dawn L Earl7, Boris Keren8, Olga Levchenko9, Sinje Geuer10, Sarah Verheyen11, Diana Johnson12, Yuri A Zarate13, Miroslava Hančárová14, David J Amor15, E Martina Bebin16, Jasmin Blatterer11, Alfredo Brusco17, Gerarda Cappuccio18, Joel Charrow19, Nicolas Chatron20, Gregory M Cooper4, Thomas Courtin8, Elena Dadali9, Julien Delafontaine21, Ennio Del Giudice22, Martine Doco23, Ganka Douglas24, Astrid Eisenkölbl25, Tara Funari24, Giuliana Giannuzzi1, Ursula Gruber-Sedlmayr26, Nicolas Guex27, Delphine Heron8, Øystein L Holla28, Anna C E Hurst29, Jane Juusola24, David Kronn30, Alexander Lavrov9, Crystle Lee31, Séverine Lorrain32, Else Merckoll33, Anna Mikhaleva1, Jennifer Norman34, Sylvain Pradervand35, Darina Prchalová14, Lindsay Rhodes24, Victoria R Sanders19, Zdeněk Sedláček14, Heidelis A Seebacher11, Elizabeth A Sellars13, Fabio Sirchia36, Toshiki Takenouchi37, Akemi J Tanaka38, Heidi Taska-Tench19, Elin Tønne5, Kristian Tveten28, Giuseppina Vitiello22, Markéta Vlčková14, Tomoko Uehara37, Caroline Nava8, Binnaz Yalcin39, Kenjiro Kosaki37, Dian Donnai3, Stefan Mundlos10, Nicola Brunetti-Pierri18, Wendy K Chung38, Alexandre Reymond40.
Abstract
The ALF transcription factor paralogs, AFF1, AFF2, AFF3, and AFF4, are components of the transcriptional super elongation complex that regulates expression of genes involved in neurogenesis and development. We describe an autosomal dominant disorder associated with de novo missense variants in the degron of AFF3, a nine amino acid sequence important for its binding to ubiquitin ligase, or with de novo deletions of this region. The sixteen affected individuals we identified, along with two previously reported individuals, present with a recognizable pattern of anomalies, which we named KINSSHIP syndrome (KI for horseshoe kidney, NS for Nievergelt/Savarirayan type of mesomelic dysplasia, S for seizures, H for hypertrichosis, I for intellectual disability, and P for pulmonary involvement), partially overlapping the AFF4-associated CHOPS syndrome. Whereas homozygous Aff3 knockout mice display skeletal anomalies, kidney defects, brain malformations, and neurological anomalies, knockin animals modeling one of the microdeletions and the most common of the missense variants identified in affected individuals presented with lower mesomelic limb deformities like KINSSHIP-affected individuals and early lethality, respectively. Overexpression of AFF3 in zebrafish resulted in body axis anomalies, providing some support for the pathological effect of increased amount of AFF3. The only partial phenotypic overlap of AFF3- and AFF4-associated syndromes and the previously published transcriptome analyses of ALF transcription factors suggest that these factors are not redundant and each contributes uniquely to proper development.Entities:
Keywords: AFF3; AFF4; horseshoe kidney; intellectual disability; mesomelic dysplasia
Year: 2021 PMID: 33961779 PMCID: PMC8206167 DOI: 10.1016/j.ajhg.2021.04.001
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025